TopicNeuro

electrophysiology

50 Seminars18 Positions11 ePosters

Latest

PositionNeuroscience

Dr. Tom Franken

Washington University
St. Louis, USA
Jan 4, 2026

A postdoctoral position is available in Dr. Tom Franken’s laboratory in the Department of Neuroscience at the Washington University School of Medicine in St. Louis. The project will study the neural circuits that parse visual scenes into organized collections of objects. We use a variety of techniques including high-density electrophysiology, behavior, optogenetics, and viral targeting in non-human primates. For more information on the lab, please visit sites.wustl.edu/frankenlab/. The PI is committed to mentoring and to nurturing a creative, thoughtful and collaborative lab culture. The laboratory is in an academic setting in the Department of Neuroscience at the Washington University School of Medicine in St. Louis, a large and collaborative scientific community. This provides an ideal environment to train, conduct research, and launch a career in science. Postdoctoral appointees at Washington University receive a competitive salary and a generous benefits package (hr.wustl.edu/benefits/). WashU Neuroscience is consistently ranked as one of the top 10 places worldwide for neuroscience research and offers an outstanding interdisciplinary training environment for early career researchers. In addition to high-quality research facilities, career and professional development training for postdoctoral researchers is provided through the Career Center, Teaching Center, Office of Postdoctoral Affairs, and campus groups. St. Louis is a city rich in culture, green spaces, free museums, world-class restaurants, and thriving music and arts scenes. On top of it all, St. Louis is affordable and commuting to campus is stress-free, whether you go by foot, bike, public transit, or car. The area combines the attractions of a major city with affordable lifestyle opportunities (postdoc.wustl.edu/prospective-postdocs/why-st-louis/). Washington University is dedicated to building a diverse community of individuals who are committed to contributing to an inclusive environment – fostering respect for all and welcoming individuals from diverse backgrounds, experiences and perspectives. Individuals with a commitment to these values are encouraged to apply. Additional information on being a postdoc at Washington University in St. Louis can be found at neuroscience.wustl.edu/education/postdoctoral-research/ and postdoc.wustl.edu/prospective-postdocs. Required Qualifications Ph.D. (or equivalent doctoral) degree in neuroscience (broadly defined). Strong background in either electrophysiology, behavioral techniques or scientific programming/machine learning. Preferred Qualifications Experience with training of larger animals. Experience with electrophysiology. Experience with studies of the visual system. Ability to think creatively to solve problems. Well organized and attention to detail. Excellent oral and written communication skills. Team player with a high level of initiative and motivation. Working Conditions This position works in a laboratory environment with potential exposure to biological and chemical hazards. The individual must be physically able to wear protective equipment and to provide standard care to research animals. Salary Range Base pay is commensurate with experience. Applicant Special Instructions Applicants should submit the following materials to Dr. Tom Franken at ftom@wustl.edu: 1) A cover letter explaining how their interest in the position matches their background and career goals. 2) CV or Biosketch. 3) Contact information for at least three professional references. Accommodation If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request. Pre-Employment Screening All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening. Benefits Statement Washington University in St. Louis is committed to providing a comprehensive and competitive benefits package to our employees. Benefits eligibility is subject to employment status, full-time equivalent (FTE) workload, and weekly standard hours. Please visit our website at https://hr.wustl.edu/benefits/ to view a summary of benefits. EEO/AA Statement Washington University in St. Louis is committed to the principles and practices of equal employment opportunity and especially encourages applications by those from underrepresented groups. It is the University’s policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information. Diversity Statement Washington University is dedicated to building a diverse community of individuals who are committed to contributing to an inclusive environment – fostering respect for all and welcoming individuals from diverse backgrounds, experiences and perspectives. Individuals with a commitment to these values are encouraged to apply.

PositionNeuroscience

Dr. Michele Insanally

University of Pittsburgh
Pittsburgh, PA
Jan 4, 2026

The Insanally Lab is hiring postdocs to study the neural basis of auditory perception and learning. We incorporate a wide range of techniques including behavioral paradigms, in vivo multi-region neural recordings, optogenetics, chemogenetics, fiber photometry, and novel computational methods. Our lab is super supportive, collaborative, and we take mentoring seriously! Located at Pitt, our lab is part of a large systems neuroscience community that includes CNBC and CMU. For inquiries, feel free to reach out to me here: mni@pitt.edu. To find out more about our work, visit Insanallylab.com

PositionNeuroscience

Dr. Rudy Behnia

Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University
New York, NY
Jan 4, 2026

The Behnia Lab, is seeking to hire a Postdoctoral Research Scientist to assist with studies on how our brains see the world around us. The overarching goal of the lab is to define the processing steps that transform light signals in photoreceptors into feature of a visual scene such as color or direction of motion. For a given visual feature, we aim to describe not only the underlying mathematic operations (algorithms) that govern a transformation, but also the neural circuits that implement these. We make extensive use of connectomics data, as well as the abundant genetic tools available in fruit flies, and collaborate extensively with theorist to build biologically constrained models of perception. We are also interested in understanding how different internal/environmental states or other sensory systems influence the visual perception and how multisensory representations are used for higher cognitive functions such as learning and navigation. We invite to you review our website for more details about our work: http://behnialab.neuroscience.columbia.edu. Example projects include: 1/ A multidisciplinary collaboration with the laboratory of Ashok Litwin-Kumar at the Center for Theoretical Neuroscience, aimed at defining circuit mechanisms underlying multisensory learning, 2/ Investigating the role of neuromodulatory systems in color processing. Please contact Rudy Behnia directly at rb3161@columbia.edu for more details. The Behnia lab is part of the Columbia University’s Mortimer B. Zuckerman Mind Brain Behavior Institute (the Zuckerman Institute) brings together world-class researchers from varied scientific disciplines to explore aspects of mind and brain, through the exchange of ideas and active collaboration. The Zuckerman Institute’s home, the Jerome L. Greene Science Center is a state-of-the-art facility on Columbia’s Manhattanville campus. Situated in the heart of Manhattan in New York City, the Zuckerman Institute houses over 50 laboratories employing a broad range of interdisciplinary approaches to transform our understanding of the mind and brain. In this highly collaborative environment, experimental, computational, and theoretical labs work together to gain critical insights into how the brain develops, performs, endures and recovers. The Zuckerman Institute provides multiple levels of support for postdoctoral researchers (https://zuckermaninstitute.columbia.edu/postdocs). The Postdoc Program provides postdocs with an enriched research environment to advance their scientific training and support their professional growth. This includes frameworks to build a professional network of mentors and peers, through the personal board of advisors, as well as leadership opportunities, workshops and opportunities for public engagement. The Behnia lab strives to provide a supportive environment where creativity, independence, work/life balance are valued. We are strong advocates of diversity, equality, inclusion and belonging. We encourage application from applicants from diverse backgrounds. Prior experience in quantitative analysis of neuronal recordings and/or behavior and related programming skills (Python, version control, databases) are required. Prior expertise with in vivo imaging, electrophysiological recordings or behavioral studies, as well as superior motivation, drive and demonstrated aptitude for carrying out independent research are highly desirable qualifications. In addition, the ideal candidate would seek to work in a highly diverse and collaborative environment.

PositionNeuroscience

Dr. Rudy Behnia

Mortimer B. Zuckerman Mind Brain Behavior Institute
New York City, NY
Jan 4, 2026

The Behnia Lab, is seeking to hire a Postdoctoral Research Scientist to assist with studies on how our brains see the world around us. The overarching goal of the lab is to define the processing steps that transform light signals in photoreceptors into feature of a visual scene such as color or direction of motion. For a given visual feature, we aim to describe not only the underlying mathematic operations (algorithms) that govern a transformation, but also the neural circuits that implement these. We make extensive use of connectomics data, as well as the abundant genetic tools available in fruit flies, and collaborate extensively with theorist to build biologically constrained models of perception. We are also interested in understanding how different internal/environmental states or other sensory systems influence the visual perception and how multisensory representations are used for higher cognitive functions such as learning and navigation. We invite to you review our website for more details about our work: http://behnialab.neuroscience.columbia.edu. Example projects include: 1/ A multidisciplinary collaboration with the laboratory of Ashok Litwin-Kumar at the Center for Theoretical Neuroscience, aimed at defining circuit mechanisms underlying multisensory learning, 2/ Investigating the role of neuromodulatory systems in color processing. Please contact Rudy Behnia directly at rb3161@columbia.edu for more details. The Behnia lab is part of the Columbia University’s Mortimer B. Zuckerman Mind Brain Behavior Institute (the Zuckerman Institute) brings together world-class researchers from varied scientific disciplines to explore aspects of mind and brain, through the exchange of ideas and active collaboration. The Zuckerman Institute’s home, the Jerome L. Greene Science Center is a state-of-the-art facility on Columbia’s Manhattanville campus. Situated in the heart of Manhattan in New York City, the Zuckerman Institute houses over 50 laboratories employing a broad range of interdisciplinary approaches to transform our understanding of the mind and brain. In this highly collaborative environment, experimental, computational, and theoretical labs work together to gain critical insights into how the brain develops, performs, endures and recovers. The Zuckerman Institute provides multiple levels of support for postdoctoral researchers (https://zuckermaninstitute.columbia.edu/postdocs). The Postdoc Program provides postdocs with an enriched research environment to advance their scientific training and support their professional growth. This includes frameworks to build a professional network of mentors and peers, through the personal board of advisors, as well as leadership opportunities, workshops and opportunities for public engagement. The Behnia lab strives to provide a supportive environment where creativity, independence, work/life balance are valued. We are strong advocates of diversity, equality, inclusion and belonging. We encourage application from applicants from diverse backgrounds.

PositionNeuroscience

Dr. Loren Frank

University of California, San Francisco
San Francisco, USA
Jan 4, 2026

The Frank Lab at the University of California, San Francisco is looking for a Junior Specialist Technician to begin work January 2021 or later. This is a full-time paid position with a two-year minimum commitment required. During this time, the technician will work directly with a postdoctoral fellow and may also contribute to other lab projects as time allows. The lab investigates the neural underpinnings of learning and memory by collecting in vivo electrophysiological recordings from the hippocampus of rats while they learn and perform complex, memory-dependent behaviors. We have developed cutting-edge decoding algorithms to capture neural representations of spatial location as rats navigate an environment. The specific project aims to measure how such spatial representations are altered in aged rats compared to young rats and assess whether changes in spatial representation might drive changes in performance of a memory-dependent task. Please reach out to Anna Gillespie (postdoc) if interested. Responsibilities include: Handling and behavioral training of rats Construction of microelectrode drives Participation in rat implant surgeries Development of behavioral and neural data analyses Collection of large scale electrophysiological and behavioral datasets

PositionNeuroscience

Dr Guillermina López-Bendito

Institute of Neuroscience of Alicante (CSIC-UMH)
Spain, Alicante
Jan 4, 2026

The López-Bendito Lab is interested in understanding and uncovering the principles underlying the development of sensory circuits with emphasis on the role of the thalamus in the development of cortical sensory maps. Furthermore, we are developing strategies for circuit restoration in sensory deprived mice. We are seeking for two (2) highly motivated postdoctoral scientists to investigate the cellular and molecular mechanisms involved in sensory circuit glia-to-neuron reprogramming. This 3-years project funded by La Caixa Foundation aims to understand the rules for region-specific reprogramming with the ultimate goal of recovery sensory thalamocortical circuits in sensory deprived mice. Applicants should have a proven track record and an independent working style.

PositionNeuroscience

Ethan Goldberg

The University of Pennsvylvania
Philadelphia, PA, U.S.A.
Jan 4, 2026

A postdoctoral fellowship position is available to study mechanisms genetic epilepsies of childhood in experimental model systems. The lab studies ion channel variants expressed in heterologous systems; neurons and organoids derived from human embryonic stem cells from human patients; cell profiling/transcriptomics; cellular neurophysiology and synaptic transmission in acute brain slices prepared from mice; and 2P calcium imaging and electrophysiology in awake, behaving experimental animals. Recent graduate with a Ph.D. in Neuroscience or applied field (electrical or biomedical engineering; computer science; cellular and molecular biology). Prior experience with electrophysiology, imaging, transcriptomics, and/or computational neuroscience, is preferred. Recent publications from the lab include: -- Favero, M., Sotuyo, N.P., Lopez, E., Kearney, J.A., Goldberg, E.M. : A transient developmental window of fast-spiking interneuron dysfunction in a mouse model of Dravet syndrome. The Journal of Neuroscience 38(36): 7912-7927, September 2018. PMCID: PMC6125809 -- Goff, K.M., Goldberg, E.M.: Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet Syndrome. Elife July 2019. PMCID: PMC6629374 -- Tran, C.H., Vaiana, M., Nakuci, J., Somarowthu, A., Goff, K.M., Goldstein, N., Murthy, P., Muldoon, S.F., Goldberg, E.M.: Interneuron desynchronization precedes seizures in a mouse model of Dravet syndrome. Journal of Neuroscience 40(13): 2764-2775, May 2020. PMCID: PMC7096149 -- Zaman, T., Helbig, K.L., Clatot, J., […] Goldberg, E.M. : SCN3A-related neurodevelopmental disorder: A spectrum of epilepsy and brain malformation. Ann Neurol doi: 10.1002/ana.25809, Online ahead of print 2020.

PositionNeuroscience

Prof. Ross Williamson

University of Pittsburgh
Pittsburgh, PA, USA
Jan 4, 2026

The Williamson Laboratory investigates the organization and function of auditory cortical projection systems in behaving mice. We use a variety of state-of-the-art tools to probe the neural circuits of awake mice – these include two-photon calcium imaging and high-channel count electrophysiology (both with single-cell optogenetic perturbations), head-fixed behaviors (including virtual reality), and statistical approaches for neural characterization. Details on the research focus and approaches of the laboratory can be found here: https://www.williamsonlaboratory.com/research/

PositionNeuroscience

Prof. Carmen Varela

Florida Atlantic University
Jupiter, Florida
Jan 4, 2026

Gain expertise in rodent electrophysiology and behavior studying thalamic cellular and network mechanisms of sleep and memory consolidation. We have several openings to study the mechanisms of synaptic plasticity and cellular spike dynamics that contribute to episodic memory consolidation during sleep. Trainees will gain expertise in systems neuroscience using electrophysiology (cell ensemble and LFP recording) and behavior in rats, as well as expertise on the thalamic molecular and cellular mechanisms underlying normal and disrupted sleep-dependent memory consolidation and the use of non-invasive technologies to regulate them. Some of the projects are part of collaborations with Harvard University and the Scripps Florida Institute.

PositionNeuroscience

Marsa

Laboratory of Dr. Panayiota Poirazi at IMBB-FORTH
IMBB-FORTH
Jan 4, 2026

The successful applicant will work on a multidisciplinary collaborative project aiming to determine the importance of cortical engram cells in memory formation and storage and probe the role of cortical memory engrams in the generation and retrieval of a sensory-based memory. The project as a whole combines computational modeling, electrophysiology, calcium imaging techniques, and molecular and behavioral experiments. First, the biophysical properties of engrams will be identified in a cortical area of interest, and their functional role will be unraveled in vivo. Then, computational modeling will be used to determine the role of engram cells during memory recall. This project is a collaboration between the Florey Institute of Neuroscience and Mental Health in Melbourne, Australia (Prof. L. Palmer), and the University of Dublin, Ireland (Prof. T. Ryan).

PositionNeuroscience

Alberto Bacci

ICM - Institut du Cerveau | Paris Brain Institute
47 Boulevard de l'Hopital, 75013 Paris, France
Jan 4, 2026

The successful candidate will work on inhibitory circuits of the prefrontal cortex of mice. In particular, they will study the properties and plasticity of synapses connecting a rich diversity of prefrontal cortical neuron subtypes. The candidate will also perform and analyze electrophysiological recordings in vivo, using high-density Neuropixels probes. This project is part of an ERA-Net NEURON international consortium and focuses on the rich diversity of GABAergic interneurons and their impact on the functional states of prefrontal cortical networks in healthy and diseased states.

PositionNeuroscience

Prof. Dr. Caspar Schwiedrzik

German Primate Center (DPZ) - Leibniz Institute for Primate Research
Göttingen, Germany
Jan 4, 2026

The Perception and Plasticity Group of Caspar Schwiedrzik at the DPZ is looking for an outstanding postdoc interested in studying the neural basis of high-dimensional category learning in vision. The project investigates neural mechanisms of category learning at the level of circuits and single cells, utilizing electrophysiology, functional magnetic resonance imaging, behavioral testing in humans and non-human primates, and computational modeling. It is funded by an ERC Consolidator Grant (Acronym DimLearn; “Flexible Dimensionality of Representational Spaces in Category Learning”). The postdoc’s project will focus on investigating the neural basis of visual category learning in macaque monkeys combining chronic multi-electrode electrophysiological recordings and electrical microstimulation. In addition, the postdoc will have the opportunity to cooperate with other lab members on parallel computational investigations using artificial neural networks as well as comparative research exploring the same questions in humans. The postdoc will play a key role in our research efforts in this area. The lab is located at Ruhr-University Bochum and the German Primate Center in Göttingen. At both locations, the lab is embedded into interdisciplinary research centers with international faculty and students pursuing cutting-edge research in cognitive and computational neuroscience. The main site for this part of the project will be Göttingen. The postdoc will have access to state-of-the-art electrophysiology, an imaging center with a dedicated 3T research scanner, and behavioral setups. The project will be conducted in close collaboration with the labs of Fabian Sinz, Alexander Gail, and Igor Kagan.

SeminarNeuroscience

Consciousness at the edge of chaos

Martin Monti
University of California Los Angeles
Dec 12, 2025

Over the last 20 years, neuroimaging and electrophysiology techniques have become central to understanding the mechanisms that accompany loss and recovery of consciousness. Much of this research is performed in the context of healthy individuals with neurotypical brain dynamics. Yet, a true understanding of how consciousness emerges from the joint action of neurons has to account for how severely pathological brains, often showing phenotypes typical of unconsciousness, can nonetheless generate a subjective viewpoint. In this presentation, I will start from the context of Disorders of Consciousness and will discuss recent work aimed at finding generalizable signatures of consciousness that are reliable across a spectrum of brain electrophysiological phenotypes focusing in particular on the notion of edge-of-chaos criticality.

SeminarNeuroscience

Unpacking the role of the medial septum in spatial coding in the medial entorhinal cortex

Jennifer Robinson
McGill University
Sep 11, 2025
SeminarNeuroscienceRecording

Fear learning induces synaptic potentiation between engram neurons in the rat lateral amygdala

Kenneth Hayworth
Carboncopies Foundation & BPF Aspirational Neuroscience
Apr 22, 2025

Fear learning induces synaptic potentiation between engram neurons in the rat lateral amygdala. This study by Marios Abatis et al. demonstrates how fear conditioning strengthens synaptic connections between engram cells in the lateral amygdala, revealed through optogenetic identification of neuronal ensembles and electrophysiological measurements. The work provides crucial insights into memory formation mechanisms at the synaptic level, with implications for understanding anxiety disorders and developing targeted interventions. Presented by Dr. Kenneth Hayworth, this journal club will explore the paper's methodology linking engram cell reactivation with synaptic plasticity measurements, and discuss implications for memory decoding research.

SeminarNeuroscience

Mouse Motor Cortex Circuits and Roles in Oromanual Behavior

Gordon Shepherd
Northwestern University
Jan 14, 2025

I’m interested in structure-function relationships in neural circuits and behavior, with a focus on motor and somatosensory areas of the mouse’s cortex involved in controlling forelimb movements. In one line of investigation, we take a bottom-up, cellularly oriented approach and use optogenetics, electrophysiology, and related slice-based methods to dissect cell-type-specific circuits of corticospinal and other neurons in forelimb motor cortex. In another, we take a top-down ethologically oriented approach and analyze the kinematics and cortical correlates of “oromanual” dexterity as mice handle food. I'll discuss recent progress on both fronts.

SeminarNeuroscienceRecording

Combined electrophysiological and optical recording of multi-scale neural circuit dynamics

Chris Lewis
University of Zurich
Apr 30, 2024

This webinar will showcase new approaches for electrophysiological recordings using our silicon neural probes and surface arrays combined with diverse optical methods such as wide-field or 2-photon imaging, fiber photometry, and optogenetic perturbations in awake, behaving mice. Multi-modal recording of single units and local field potentials across cortex, hippocampus and thalamus alongside calcium activity via GCaMP6F in cortical neurons in triple-transgenic animals or in hippocampal astrocytes via viral transduction are brought to bear to reveal hitherto inaccessible and under-appreciated aspects of coordinated dynamics in the brain.

SeminarNeuroscienceRecording

Closed-loop deep brain stimulation as a neuroprosthetic of dopaminergic circuits – Current evidence and future opportunities; Spatial filtering to enhance signal processing in invasive neurophysiology

Wolf-Julian Neumann, MD & Prof. Victoria Peterson, PhD
Charité – Universitätsmedizin Berlin, Germany / IMAL-UNL-CONICET, Sata Fe, Argentinia
Feb 15, 2024

On Thursday February 15th, we will host Victoria Peterson and Julian Neumann. Victoria will tell us about “Spatial filtering to enhance signal processing in invasive neurophysiology”. Besides his scientific presentation on “Closed-loop deep brain stimulation as a neuroprosthetic of dopaminergic circuits – Current evidence and future opportunities”, Julian will give us a glimpse at the person behind the science. The talks will be followed by a shared discussion. Note: The talks will exceptionally be held at 10 ET / 4PM CET. You can register via talks.stimulatingbrains.org to receive the (free) Zoom link!

SeminarNeuroscienceRecording

State-of-the-Art Spike Sorting with SpikeInterface

Samuel Garcia and Alessio Buccino
CRNS, Lyon, France and Allen Institute for Neural Dynamics, Seattle, USA
Nov 7, 2023

This webinar will focus on spike sorting analysis with SpikeInterface, an open-source framework for the analysis of extracellular electrophysiology data. After a brief introduction of the project (~30 mins) highlighting the basics of the SpikeInterface software and advanced features (e.g., data compression, quality metrics, drift correction, cloud visualization), we will have an extensive hands-on tutorial (~90 mins) showing how to use SpikeInterface in a real-world scenario. After attending the webinar, you will: (1) have a global overview of the different steps involved in a processing pipeline; (2) know how to write a complete analysis pipeline with SpikeInterface.

SeminarNeuroscience

Consolidation of remote contextual memory in the neocortical memory engram

Jun-Hyeong Cho
Oct 26, 2023

Recent studies identified memory engram neurons, a neuronal population that is recruited by initial learning and is reactivated during memory recall.  Memory engram neurons are connected to one another through memory engram synapses in a distributed network of brain areas.  Our central hypothesis is that an associative memory is encoded and consolidated by selective strengthening of engram synapses.  We are testing this hypothesis, using a combination of engram cell labeling, optogenetic/chemogenetic, electrophysiological, and virus tracing approaches in rodent models of contextual fear conditioning.  In this talk, I will discuss our findings on how synaptic plasticity in memory engram synapses contributes to the acquisition and consolidation of contextual fear memory in a distributed network of the amygdala, hippocampus, and neocortex.

SeminarNeuroscienceRecording

Rodents to Investigate the Neural Basis of Audiovisual Temporal Processing and Perception

Ashley Schormans
BrainsCAN, Western University, Canada.
Sep 27, 2023

To form a coherent perception of the world around us, we are constantly processing and integrating sensory information from multiple modalities. In fact, when auditory and visual stimuli occur within ~100 ms of each other, individuals tend to perceive the stimuli as a single event, even though they occurred separately. In recent years, our lab, and others, have developed rat models of audiovisual temporal perception using behavioural tasks such as temporal order judgments (TOJs) and synchrony judgments (SJs). While these rodent models demonstrate metrics that are consistent with humans (e.g., perceived simultaneity, temporal acuity), we have sought to confirm whether rodents demonstrate the hallmarks of audiovisual temporal perception, such as predictable shifts in their perception based on experience and sensitivity to alterations in neurochemistry. Ultimately, our findings indicate that rats serve as an excellent model to study the neural mechanisms underlying audiovisual temporal perception, which to date remains relativity unknown. Using our validated translational audiovisual behavioural tasks, in combination with optogenetics, neuropharmacology and in vivo electrophysiology, we aim to uncover the mechanisms by which inhibitory neurotransmission and top-down circuits finely control ones’ perception. This research will significantly advance our understanding of the neuronal circuitry underlying audiovisual temporal perception, and will be the first to establish the role of interneurons in regulating the synchronized neural activity that is thought to contribute to the precise binding of audiovisual stimuli.

SeminarNeuroscienceRecording

Adaptive deep brain stimulation to treat gait disorders in Parkinson's disease; Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson's disease

Doris Wang, MD, PhD & Stephanie Cernera, PhD
University of California, San Francisco, USA
Aug 31, 2023

On Friday, August 31st we will host Stephanie Cernera & Doris Wang! Stephanie Cernera, PhD, is a postdoctoral research fellow in the Starr lab at University of California San Francisco. She will tell us about “Personalized chronic adaptive deep brain stimulation outperforms conventional stimulation in Parkinson’s Disease”. Doris Wang, MD, PhD, is a neurosurgeon and assistant professor at the University of California San Francisco. Apart from her scientific presentation about “Adaptive Deep Brain Stimulation to Treat Gait Disorders in Parkinson’s Disease”, she will give us a glimpse at the “Person behind the science”. The talks will be followed by a shared discussion. You can register via talks.stimulatingbrains.org to receive the (free) Zoom link!

SeminarNeuroscience

The balanced brain: two-photon microscopy of inhibitory synapse formation

Corette Wierenga
Donders Institute
May 11, 2023

Coordination between excitatory and inhibitory synapses (providing positive and negative signals respectively) is required to ensure proper information processing in the brain. Many brain disorders, especially neurodevelopental disorders, are rooted in a specific disturbance of this coordination. In my research group we use a combination of two-photon microscopy and electrophisiology to examine how inhibitory synapses are fromed and how this formation is coordinated with nearby excitatroy synapses.

SeminarNeuroscience

Distinct contributions of different anterior frontal regions to rule-guided decision-making in primates: complementary evidence from lesions, electrophysiology, and neurostimulation

Mark Buckley
Oxford University
May 5, 2023

Different prefrontal areas contribute in distinctly different ways to rule-guided behaviour in the context of a Wisconsin Card Sorting Test (WCST) analog for macaques. For example, causal evidence from circumscribed lesions in NHPs reveals that dorsolateral prefrontal cortex (dlPFC) is necessary to maintain a reinforced abstract rule in working memory, orbitofrontal cortex (OFC) is needed to rapidly update representations of rule value, and the anterior cingulate cortex (ACC) plays a key role in cognitive control and integrating information for correct and incorrect trials over recent outcomes. Moreover, recent lesion studies of frontopolar cortex (FPC) suggest it contributes to representing the relative value of unchosen alternatives, including rules. Yet we do not understand how these functional specializations relate to intrinsic neuronal activities nor the extent to which these neuronal activities differ between different prefrontal regions. After reviewing the aforementioned causal evidence I will present our new data from studies using multi-area multi-electrode recording techniques in NHPs to simultaneously record from four different prefrontal regions implicated in rule-guided behaviour. Multi-electrode micro-arrays (‘Utah arrays’) were chronically implanted in dlPFC, vlPFC, OFC, and FPC of two macaques, allowing us to simultaneously record single and multiunit activity, and local field potential (LFP), from all regions while the monkey performs the WCST analog. Rule-related neuronal activity was widespread in all areas recorded but it differed in degree and in timing between different areas. I will also present preliminary results from decoding analyses applied to rule-related neuronal activities both from individual clusters and also from population measures. These results confirm and help quantify dynamic task-related activities that differ between prefrontal regions. We also found task-related modulation of LFPs within beta and gamma bands in FPC. By combining this correlational recording methods with trial-specific causal interventions (electrical microstimulation) to FPC we could significantly enhance and impair animals performance in distinct task epochs in functionally relevant ways, further consistent with an emerging picture of regional functional specialization within a distributed framework of interacting and interconnected cortical regions.

SeminarNeuroscienceRecording

More than a beast growing in a passive brain: excitation and inhibition drive epilepsy and glioma progression

Gilles Huberfeld
Hôpital Fondation Adolphe de Rothschild
Apr 12, 2023

Gliomas are brain tumors formed by networks of connected tumor cells, nested in and interacting with neuronal networks. Neuronal activities interfere with tumor growth and occurrence of seizures affects glioma prognosis, while the developing tumor triggers seizures in the infiltrated cortex. Oncometabolites produced by tumor cells and neurotransmitters affect both the generation of epileptic activities by neurons and the growth of glioma cells through synaptic-related mechanisms, involving both GABAergic / Chloride pathways and glutamatergic signaling. From a clinical sight, epilepsy occurrence is beneficial to glioma prognosis but growing tumors are epileptogenic, which constitutes a paradox. This lecture will review how inhibitory and excitatory signaling drives glioma growth and how epileptic and oncological processes are interfering, with a special focus on the human brain.

SeminarNeuroscience

A specialized role for entorhinal attractor dynamics in combining path integration and landmarks during navigation

Malcolm Campbell
Harvard
Mar 9, 2023

During navigation, animals estimate their position using path integration and landmarks. In a series of two studies, we used virtual reality and electrophysiology to dissect how these inputs combine to generate the brain’s spatial representations. In the first study (Campbell et al., 2018), we focused on the medial entorhinal cortex (MEC) and its set of navigationally-relevant cell types, including grid cells, border cells, and speed cells. We discovered that attractor dynamics could explain an array of initially puzzling MEC responses to virtual reality manipulations. This theoretical framework successfully predicted both MEC grid cell responses to additional virtual reality manipulations, as well as mouse behavior in a virtual path integration task. In the second study (Campbell*, Attinger* et al., 2021), we asked whether these principles generalize to other navigationally-relevant brain regions. We used Neuropixels probes to record thousands of neurons from MEC, primary visual cortex (V1), and retrosplenial cortex (RSC). In contrast to the prevailing view that “everything is everywhere all at once,” we identified a unique population of MEC neurons, overlapping with grid cells, that became active with striking spatial periodicity while head-fixed mice ran on a treadmill in darkness. These neurons exhibited unique cue-integration properties compared to other MEC, V1, or RSC neurons: they remapped more readily in response to conflicts between path integration and landmarks; they coded position prospectively as opposed to retrospectively; they upweighted path integration relative to landmarks in conditions of low visual contrast; and as a population, they exhibited a lower-dimensional activity structure. Based on these results, our current view is that MEC attractor dynamics play a privileged role in resolving conflicts between path integration and landmarks during navigation. Future work should include carefully designed causal manipulations to rigorously test this idea, and expand the theoretical framework to incorporate notions of uncertainty and optimality.

SeminarNeuroscienceRecording

Prox2+ and Runx3+ vagal sensory neurons regulate esophageal motility

Elijah Lowenstein
Birchmeier lab, Max Delbrück Center
Mar 1, 2023

Sensory neurons of the vagus nerve monitor distention and stretch in the gastrointestinal tract. We used genetically guided anatomical tracing, optogenetics and electrophysiology to identify and characterize two vagal sensory neuronal subtypes expressing Prox2 and Runx3. We show that these neuronal subtypes innervate the esophagus where they display regionalized innervation patterns. Electrophysiological analyses showed that they are both low threshold mechanoreceptors but possess different adaptation properties. Lastly, genetic ablation of Prox2 and Runx3 neurons demonstrated their essential roles for esophageal peristalsis and swallowing in freely behaving animals. Our work reveals the identity and function of the vagal neurons that provide mechanosensory feedback from the esophagus to the brain and could lead to better understanding and treatment of esophageal motility disorders.

SeminarNeuroscienceRecording

Silences, Spikes and Bursts: Three-Part Knot of the Neural Code

Richard Naud
University of Ottawa
Mar 1, 2023

When a neuron breaks silence, it can emit action potentials in a number of patterns. Some responses are so sudden and intense that electrophysiologists felt the need to single them out, labeling action potentials emitted at a particularly high frequency with a metonym – bursts. Is there more to bursts than a figure of speech? After all, sudden bouts of high-frequency firing are expected to occur whenever inputs surge. In this talk, I will discuss the implications of seeing the neural code as having three syllables: silences, spikes and bursts. In particular, I will describe recent theoretical and experimental results that implicate bursting in the implementation of top-down attention and the coordination of learning.

SeminarNeuroscience

Baby steps to breakthroughs in precision health in neurodevelopmental disorders

Shafali Spurling Jeste
Children's Hospital Los Angeles
Oct 26, 2022
SeminarNeuroscience

High capacity electrophysiology: Lots more data, problematic analysis

Tim Harris
Janelia Research Campus, U.S.A
Sep 30, 2022
SeminarNeuroscience

Multi-level theory of neural representations in the era of large-scale neural recordings: Task-efficiency, representation geometry, and single neuron properties

SueYeon Chung
NYU/Flatiron
Sep 16, 2022

A central goal in neuroscience is to understand how orchestrated computations in the brain arise from the properties of single neurons and networks of such neurons. Answering this question requires theoretical advances that shine light into the ‘black box’ of representations in neural circuits. In this talk, we will demonstrate theoretical approaches that help describe how cognitive and behavioral task implementations emerge from the structure in neural populations and from biologically plausible neural networks. First, we will introduce an analytic theory that connects geometric structures that arise from neural responses (i.e., neural manifolds) to the neural population’s efficiency in implementing a task. In particular, this theory describes a perceptron’s capacity for linearly classifying object categories based on the underlying neural manifolds’ structural properties. Next, we will describe how such methods can, in fact, open the ‘black box’ of distributed neuronal circuits in a range of experimental neural datasets. In particular, our method overcomes the limitations of traditional dimensionality reduction techniques, as it operates directly on the high-dimensional representations, rather than relying on low-dimensionality assumptions for visualization. Furthermore, this method allows for simultaneous multi-level analysis, by measuring geometric properties in neural population data, and estimating the amount of task information embedded in the same population. These geometric frameworks are general and can be used across different brain areas and task modalities, as demonstrated in the work of ours and others, ranging from the visual cortex to parietal cortex to hippocampus, and from calcium imaging to electrophysiology to fMRI datasets. Finally, we will discuss our recent efforts to fully extend this multi-level description of neural populations, by (1) investigating how single neuron properties shape the representation geometry in early sensory areas, and by (2) understanding how task-efficient neural manifolds emerge in biologically-constrained neural networks. By extending our mathematical toolkit for analyzing representations underlying complex neuronal networks, we hope to contribute to the long-term challenge of understanding the neuronal basis of tasks and behaviors.

SeminarNeuroscience

New Insights into the Neural Machinery of Face Recognition

Winrich Freiwald
Rockefeller
Jul 12, 2022
SeminarNeuroscience

Imperial Neurotechnology 2022 - Annual Research Symposium

Marcus Kaiser, Sarah Marzi, Giuseppe Gava, Gema Vera Gonzalez, Matteo Vinao-Carl, Sihao Lu, Hayriye Cagnan
Nottingham University, Imperial College, University of Oxford
Jul 5, 2022

A diverse mix of neurotechnology talks and posters from researchers at Imperial and beyond. Visit our event page to find out more. The event is in-person but talk sessions will be broadcast via Teams.

SeminarNeuroscienceRecording

Pynapple: a light-weight python package for neural data analysis - webinar + tutorial

Adrien Peyrache and Guillaume Viejo
McGill University, Canada
Jun 29, 2022

In systems neuroscience, datasets are multimodal and include data-streams of various origins: multichannel electrophysiology, 1- or 2-p calcium imaging, behavior, etc. Often, the exact nature of data streams are unique to each lab, if not each project. Analyzing these datasets in an efficient and open way is crucial for collaboration and reproducibility. In this combined webinar and tutorial, Adrien Peyrache and Guillaume Viejo will present Pynapple, a Python-based data analysis pipeline for systems neuroscience. Designed for flexibility and versatility, Pynapple allows users to perform cross-modal neural data analysis via a common programming approach which facilitates easy sharing of both analysis code and data.

SeminarNeuroscienceRecording

Pynapple: a light-weight python package for neural data analysis - webinar + tutorial

Adrien Peyrache and Guillaume Viejo
McGill University, Canada
Jun 28, 2022

In systems neuroscience, datasets are multimodal and include data-streams of various origins: multichannel electrophysiology, 1- or 2-p calcium imaging, behavior, etc. Often, the exact nature of data streams are unique to each lab, if not each project. Analyzing these datasets in an efficient and open way is crucial for collaboration and reproducibility. In this combined webinar and tutorial, Adrien Peyrache and Guillaume Viejo will present Pynapple, a Python-based data analysis pipeline for systems neuroscience. Designed for flexibility and versatility, Pynapple allows users to perform cross-modal neural data analysis via a common programming approach which facilitates easy sharing of both analysis code and data.

SeminarNeuroscienceRecording

What the fly’s eye tells the fly’s brain…and beyond

Gwyneth Card
Janelia Research Campus, HHMI
Jun 1, 2022

Fly Escape Behaviors: Flexible and Modular We have identified a set of escape maneuvers performed by a fly when confronted by a looming object. These escape responses can be divided into distinct behavioral modules. Some of the modules are very stereotyped, as when the fly rapidly extends its middle legs to jump off the ground. Other modules are more complex and require the fly to combine information about both the location of the threat and its own body posture. In response to an approaching object, a fly chooses some varying subset of these behaviors to perform. We would like to understand the neural process by which a fly chooses when to perform a given escape behavior. Beyond an appealing set of behaviors, this system has two other distinct advantages for probing neural circuitry. First, the fly will perform escape behaviors even when tethered such that its head is fixed and neural activity can be imaged or monitored using electrophysiology. Second, using Drosophila as an experimental animal makes available a rich suite of genetic tools to activate, silence, or image small numbers of cells potentially involved in the behaviors. Neural Circuits for Escape Until recently, visually induced escape responses have been considered a hardwired reflex in Drosophila. White-eyed flies with deficient visual pigment will perform a stereotyped middle-leg jump in response to a light-off stimulus, and this reflexive response is known to be coordinated by the well-studied giant fiber (GF) pathway. The GFs are a pair of electrically connected, large-diameter interneurons that traverse the cervical connective. A single GF spike results in a stereotyped pattern of muscle potentials on both sides of the body that extends the fly's middle pair of legs and starts the flight motor. Recently, we have found that a fly escaping a looming object displays many more behaviors than just leg extension. Most of these behaviors could not possibly be coordinated by the known anatomy of the GF pathway. Response to a looming threat thus appears to involve activation of numerous different neural pathways, which the fly may decide if and when to employ. Our goal is to identify the descending pathways involved in coordinating these escape behaviors as well as the central brain circuits, if any, that govern their activation. Automated Single-Fly Screening We have developed a new kind of high-throughput genetic screen to automatically capture fly escape sequences and quantify individual behaviors. We use this system to perform a high-throughput genetic silencing screen to identify cell types of interest. Automation permits analysis at the level of individual fly movements, while retaining the capacity to screen through thousands of GAL4 promoter lines. Single-fly behavioral analysis is essential to detect more subtle changes in behavior during the silencing screen, and thus to identify more specific components of the contributing circuits than previously possible when screening populations of flies. Our goal is to identify candidate neurons involved in coordination and choice of escape behaviors. Measuring Neural Activity During Behavior We use whole-cell patch-clamp electrophysiology to determine the functional roles of any identified candidate neurons. Flies perform escape behaviors even when their head and thorax are immobilized for physiological recording. This allows us to link a neuron's responses directly to an action.

SeminarNeuroscienceRecording

Modularity and Robustness of Frontal Cortical Networks

Nuo Li
Baylor College of Medicine, USA
May 24, 2022

Nuo Li (Baylor College of Medicine, USA) shares novel insights into coordinated interhemispheric large-scale neural network activity underpinning short-term memory in mice. Relevant techniques covered include: simultaneous multi-regional recordings using multiple 64-channel H probes during head-fixed behavior in mice. simultaneous optogenetics and population recording. analysis of population recordings to infer interactions between brain regions. Reference: Chen G, Kang B, Lindsey J, Druckmann S, Li N, (2021). Modularity and robustness of frontal cortex networks. Cell, 184(14):3717-3730.

SeminarNeuroscience

Neural Representations of Social Homeostasis

Kay M. Tye
HHMI Investigator, and Wylie Vale Chair, The Salk Institute for Biological Studies, SNL-KT
May 17, 2022

How does our brain rapidly determine if something is good or bad? How do we know our place within a social group? How do we know how to behave appropriately in dynamic environments with ever-changing conditions? The Tye Lab is interested in understanding how neural circuits important for driving positive and negative motivational valence (seeking pleasure or avoiding punishment) are anatomically, genetically and functionally arranged. We study the neural mechanisms that underlie a wide range of behaviors ranging from learned to innate, including social, feeding, reward-seeking and anxiety-related behaviors. We have also become interested in “social homeostasis” -- how our brains establish a preferred set-point for social contact, and how this maintains stability within a social group. How are these circuits interconnected with one another, and how are competing mechanisms orchestrated on a neural population level? We employ optogenetic, electrophysiological, electrochemical, pharmacological and imaging approaches to probe these circuits during behavior.

SeminarNeuroscience

What does time of day mean for vision?

Annette Allen
University of Manchester (UK)
May 5, 2022

Profound changes in the visual environment occur over the course of the day-night cycle. There is therefore a profound pressure for cells and circuits within the visual system to adjust their function over time, to match the prevailing visual environment. Here, I will discuss electrophysiological data collected from nocturnal and diurnal rodents that reveal how the visual code is ‘temporally optimised’ by 1) the retina’s circadian clock, and 2) a change in behavioural temporal niche.

SeminarNeuroscience

Elucidating the mechanism underlying Stress and Caffeine-induced motor dysfunction using a mouse model of Episodic Ataxia Type 2

Heather Snell
Albert Einstein Medical College
Apr 27, 2022

Episodic Ataxia type 2 (EA2), caused by mutations in the CACNA1A gene, results in a loss-of-function of the P/Q type calcium channel, which leads to baseline ataxia, and attacks of dyskinesia, that can last a few hours to a few days. Attacks are brought on by consumption of caffeine, alcohol, and physical or emotional stress. Interestingly, caffeine and stress are common triggers among other episodic channelopathies, as well as causing tremor or shaking in otherwise healthy adults. The mechanism underlying stress and caffeine induced motor impairment remains poorly understood. Utilizing behavior, and in vivo and in vitro electrophysiology in the tottering mouse, a well characterized mouse model of EA2, or WT mice, we first sought to elucidate the mechanism underlying stress-induced motor impairment. We found stress induces attacks in EA2 though the activation of cerebellar alpha 1 adrenergic receptors by norepinephrine (NE) through casein kinase 2 (CK2) dependent phosphorylation. This decreases SK2 channel activity, causing increased Purkinje cell irregularity and motor impairment. Knocking down or blocking CK2 with an FDA approved drug CX-4945 prevented PC irregularity and stress-induced attacks. We next hypothesized caffeine, which has been shown to increase NE levels, could induce attacks through the same alpha 1 adrenergic mechanism in EA2. We found caffeine increases PC irregularity and induces attacks through the same CK2 pathway. Block of alpha 1 adrenergic receptors, however, failed to prevent caffeine-induced attacks. Caffeine instead induces attacks through the block of cerebellar A1 adenosine receptors. This increases the release of glutamate, which interacts with mGluR1 receptors on PC, resulting in erratic firing and motor attacks. Finally, we show a novel direct interaction between mGluR1 and CK2, and inhibition of mGluR1 prior to initiation of attack, prevents the caffeine-induced increase in phosphorylation. These data elucidate the mechanism underlying stress and caffeine-induced motor impairment. Furthermore, given the success of CX-4945 to prevent stress and caffeine induced attacks, it establishes ground-work for the development of therapeutics for the treatment of caffeine and stress induced attacks in EA2 patients and possibly other episodic channelopathies.

SeminarNeuroscienceRecording

Cortex-dependent corrections as the mouse tongue reaches for and misses targets

Brendan Ito & Teja Bollu
Cornell University, USA & Salk Institute, USA
Apr 20, 2022

Brendan Ito (Cornell University, USA) and Teja Bollu (Salk Institute, USA) share unique insights into rapid online motor corrections during mouse licking, analogous to primate goal-oriented reaching. Techniques covered include large-scale single unit recording during behaviour with optogenetics, and a deep-learning-based neural network to resolve 3D tongue kinematics during licking.

SeminarNeuroscienceRecording

Sensing in Insect Wings

Ali Weber
University of Washington, USA
Apr 19, 2022

Ali Weber (University of Washington, USA) uses the the hawkmoth as a model system, to investigate how information from a small number of mechanoreceptors on the wings are used in flight control. She employs a combination of experimental and computational techniques to study how these sensors respond during flight and how one might optimally array a set of these sensors to best provide feedback during flight.

SeminarNeuroscience

2nd In-Vitro 2D & 3D Neuronal Networks Summit

Dr. Manuel Schröter, Dr. David Pamies, Dr. Silvia Ronchi, Jens Duru, Dr. Hideaki Yamamoto, Xiaohan Xue, Danny McSweeney, Dr. Katherine Czysz, Dr. Maria Sundberg
Apr 7, 2022

The event is open to everyone interested in Neuroscience, Cell Biology, Drug Discovery, Disease Modeling, and Bio/Neuroengineering! This meeting is a platform bringing scientists from all over the world together and fostering scientific exchange and collaboration.

SeminarNeuroscience

2nd In-Vitro 2D & 3D Neuronal Networks Summit

Prof. Dr. Nael Nadif Kasri, Prof. Dr. Naihe Jing, Prof. Dr. Bastian Hengerer, Prof. Dr. Janos Vörös, Dr. Bruna Paulsen, Dr. Annina Denoth-Lippuner, Dr, Jessica Sevetson, Prof. Dr. Kenneth Kosik
Apr 6, 2022

The event is open to everyone interested in Neuroscience, Cell Biology, Drug Discovery, Disease Modeling, and Bio/Neuroengineering! This meeting is a platform bringing scientists from all over the world together and fostering scientific exchange and collaboration.

SeminarNeuroscience

The french roots of electrophysiology

Gabriel Finkelstein
Mar 25, 2022

This talk looks at the subject of my biography, the German physiologist Emil du Bois-Reymond (1818–1896). With respect to his philosophy of biological reduction, his methods of electrophysiological experiment, and his co-discovery of the action potential, du Bois-Reymond is generally considered one of the founders of neuroscience. Less well known are the origins of his innovation: French writers shaped his outlook on science, just as French scientists shaped his practice in the laboratory. I contend that du Bois-Reymond’s originality is the product of his synthesis of French traditions with German concerns.

SeminarNeuroscienceRecording

NaV Long-term Inactivation Regulates Adaptation in Place Cells and Depolarization Block in Dopamine Neurons

Carmen Canavier
LSU Health Sciences Center, New Orleans
Feb 9, 2022

In behaving rodents, CA1 pyramidal neurons receive spatially-tuned depolarizing synaptic input while traversing a specific location within an environment called its place. Midbrain dopamine neurons participate in reinforcement learning, and bursts of action potentials riding a depolarizing wave of synaptic input signal rewards and reward expectation. Interestingly, slice electrophysiology in vitro shows that both types of cells exhibit a pronounced reduction in firing rate (adaptation) and even cessation of firing during sustained depolarization. We included a five state Markov model of NaV1.6 (for CA1) and NaV1.2 (for dopamine neurons) respectively, in computational models of these two types of neurons. Our simulations suggest that long-term inactivation of this channel is responsible for the adaptation in CA1 pyramidal neurons, in response to triangular depolarizing current ramps. We also show that the differential contribution of slow inactivation in two subpopulations of midbrain dopamine neurons can account for their different dynamic ranges, as assessed by their responses to similar depolarizing ramps. These results suggest long-term inactivation of the sodium channel is a general mechanism for adaptation.

SeminarNeuroscienceRecording

Norepinephrine links astrocytic activity to regulation of cortical state

Michael Reitman
Poskanzer Lab, UCSF
Jan 26, 2022

Cortical state, defined by the synchrony of population-level neuronal activity, is a key determinant of sensory perception. While many arousal-associated neuromodulators—including norepinephrine (NE)—reduce cortical synchrony, how the cortex resynchronizes following NE signaling remains unknown. Using in vivo two-photon imaging and electrophysiology in mouse visual cortex, we describe a critical role for cortical astrocytes in circuit resynchronization. We characterize astrocytes’ sensitive calcium responses to changes in behavioral arousal and NE, identify that astrocyte signaling precedes increases in cortical synchrony, and demonstrate that astrocyte-specific deletion of Adra1A alters arousal-related cortical synchrony. Our findings demonstrate that astrocytic NE signaling acts as a distinct neuromodulatory pathway, regulating cortical state and linking arousal-associated desynchrony to cortical circuit resynchronization.

SeminarNeuroscienceRecording

Distance-tuned neurons drive specialized path integration calculations in medial entorhinal cortex

Alexander Attinger
Giocomo lab, Stanford University
Jan 12, 2022

During navigation, animals estimate their position using path integration and landmarks, engaging many brain areas. Whether these areas follow specialized or universal cue integration principles remains incompletely understood. We combine electrophysiology with virtual reality to quantify cue integration across thousands of neurons in three navigation-relevant areas: primary visual cortex (V1), retrosplenial cortex (RSC), and medial entorhinal cortex (MEC). Compared with V1 and RSC, path integration influences position estimates more in MEC, and conflicts between path integration and landmarks trigger remapping more readily. Whereas MEC codes position prospectively, V1 codes position retrospectively, and RSC is intermediate between the two. Lowered visual contrast increases the influence of path integration on position estimates only in MEC. These properties are most pronounced in a population of MEC neurons, overlapping with grid cells, tuned to distance run in darkness. These results demonstrate the specialized role that path integration plays in MEC compared with other navigation-relevant cortical areas.

SeminarNeuroscience

Networking—the key to success… especially in the brain

Alexander Dunn
University of Cambridge, DAMTP
Nov 17, 2021

In our everyday lives, we form connections and build up social networks that allow us to function successfully as individuals and as a society. Our social networks tend to include well-connected individuals who link us to other groups of people that we might otherwise have limited access to. In addition, we are more likely to befriend individuals who a) live nearby and b) have mutual friends. Interestingly, neurons tend to do the same…until development is perturbed. Just like social networks, neuronal networks require highly connected hubs to elicit efficient communication at minimal cost (you can’t befriend everybody you meet, nor can every neuron wire with every other!). This talk will cover some of Alex’s work showing that microscopic (cellular scale) brain networks inferred from spontaneous activity show similar complex topology to that previously described in macroscopic human brain scans. The talk will also discuss what happens when neurodevelopment is disrupted in the case of a monogenic disorder called Rett Syndrome. This will include simulations of neuronal activity and the effects of manipulation of model parameters as well as what happens when we manipulate real developing networks using optogenetics. If functional development can be restored in atypical networks, this may have implications for treatment of neurodevelopmental disorders like Rett Syndrome.

SeminarNeuroscienceRecording

Top-down modulation of the retinal code via histaminergic neurons in the hypothalamus

Michal Rivlin
Weismann Institute
Oct 18, 2021

The mammalian retina is considered an autonomous neuronal tissue, yet there is evidence that it receives inputs from the brain in the form of retinopetal axons. A sub-population of these axons was suggested to belong to histaminergic neurons located in the tuberomammillarynucleus (TMN) of the hypothalamus. Using viral injections to the TMN, we identified these retinopetal axons and found that although few in number, they extensively branch to cover a large portion of the retina. Using Ca2+ imaging and electrophysiology, we show that histamine application increases spontaneous firing rates and alters the light responses of a significant portion of retinal ganglion cells (RGCs). Direct activation of the histaminergic axons also induced significant changes in RGCs activity. Since activity in the TMN was shown to correlate with arousal state, our data suggest the retinal code may change with the animal's behavioral state through the release of histamine from TMN histaminergic neurons.

SeminarNeuroscience

Synaptic health in Parkinson's Disease

Dayne Beccano-Kelly
Cardiff University
Aug 12, 2021

Parkinson's disease (PD) is the second most common neurodegenerative disorder, affecting 1% of over 65's; there is currently no effective treatment. Dopaminergic neuronal loss is hallmark in PD and yet despite decades of intensive research there is still no known therapeutic which will completely halt the disorder. As a result, identification of interventive therapies to reverse or prevent PD are essential. Using genetically faithful models (induced pluripotent stem cells and knock-in mice) of familial late onset PD (LRRK2 G2019S and GBA N370S) we have contributed to the literature that neuronal dysfunction precedes degeneration. Specifically, using whole cell patch clamp electrophysiology, biochemical, behavioural and molecular biological techniques, we have begun to investigate the fundamental processes that make neurons specialised i.e., synaptic function and neurotransmission. We illustrate those alterations to spontaneous neurotransmitter release, neuronal firing, and short-term plasticity as well as Ca2+ and energy dyshomeostasis, are some of the earliest observable pathological dysfunctions and are likely precursors to late-stage degeneration. These pathologies represent targets which can be manipulated to address causation, rather than the symptoms of the PD, and represent a marker that, if measurable in patients, could form the basis of early PD detection and intervention.

SeminarNeuroscience

A brain circuit for curiosity

Mehran Ahmadlou
Netherlands Institute for Neuroscience
Jul 12, 2021

Motivational drives are internal states that can be different even in similar interactions with external stimuli. Curiosity as the motivational drive for novelty-seeking and investigating the surrounding environment is for survival as essential and intrinsic as hunger. Curiosity, hunger, and appetitive aggression drive three different goal-directed behaviors—novelty seeking, food eating, and hunting— but these behaviors are composed of similar actions in animals. This similarity of actions has made it challenging to study novelty seeking and distinguish it from eating and hunting in nonarticulating animals. The brain mechanisms underlying this basic survival drive, curiosity, and novelty-seeking behavior have remained unclear. In spite of having well-developed techniques to study mouse brain circuits, there are many controversial and different results in the field of motivational behavior. This has left the functions of motivational brain regions such as the zona incerta (ZI) still uncertain. Not having a transparent, nonreinforced, and easily replicable paradigm is one of the main causes of this uncertainty. Therefore, we chose a simple solution to conduct our research: giving the mouse freedom to choose what it wants—double freeaccess choice. By examining mice in an experimental battery of object free-access double-choice (FADC) and social interaction tests—using optogenetics, chemogenetics, calcium fiber photometry, multichannel recording electrophysiology, and multicolor mRNA in situ hybridization—we uncovered a cell type–specific cortico-subcortical brain circuit of the curiosity and novelty-seeking behavior. We found in mice that inhibitory neurons in the medial ZI (ZIm) are essential for the decision to investigate an object or a conspecific. These neurons receive excitatory input from the prelimbic cortex to signal the initiation of exploration. This signal is modulated in the ZIm by the level of investigatory motivation. Increased activity in the ZIm instigates deep investigative action by inhibiting the periaqueductal gray region. A subpopulation of inhibitory ZIm neurons expressing tachykinin 1 (TAC1) modulates the investigatory behavior.

SeminarNeuroscienceRecording

“From the Sublime to the Stomatopod: the story from beginning to nowhere near the end.”

Justin Marshall
University of Queensland
Jul 12, 2021

“Call me a marine vision scientist. Some years ago - never mind how long precisely - having little or no money in my purse, and nothing particular to interest me on shore, I thought I would sail about a little and see what animals see in the watery part of the world. It is a way I have of dividing off the spectrum, and regulating circular polarisation.” Sometimes I wish I had just set out to harpoon a white whale as it would have been easier than studying stomatopod (mantis shrimp) vision. Nowhere near as much fun of course and certainly less dangerous so in this presentation I track the history of discovery and confusion that stomatopods deliver in trying to understand what the do actually see. The talk unashamedly borrows from that of Mike Bok a few weeks ago (April 13th 2021 “The Blurry Beginnings: etc” talk) as an introduction to the system (do go look at his talk again, it is beautiful!) and goes both backwards and forwards in time, trying to provide an explanation for the design of this visual system. The journey is again one of retinal anatomy and physiology, neuroanatomy, electrophysiology, behaviour and body ornaments but this time focusses more on polarisation vision (Mike covered the colour stuff well). There is a comparative section looking at the cephalopods too and by the end, I hope you will understand where we are at with trying to understand this extraordinary way of seeing the world and why we ‘pod-people’ wave our arms around so much when asked to explain; what do stomatopods see? Maybe, to butcher another quote: “mantis shrimp have been rendered visually beautiful for vision’s sake.”

SeminarNeuroscienceRecording

Imperial Neurotechnology 2021 - Annual Research Symposium

Yulong Li, Christos Kapatos, Mary Ann Go, Sonja Hofer, Oscar Bates, Christian Wilms
Peking University, SERG Technologies, Imperial College, UCL, Scientifica Ltd
Jul 7, 2021

A diverse mix of neurotechnology talks from academic and industry colleagues plus presentations from our MRes Neurotechnology students. Visit our event page to find out more and register now!

SeminarNeuroscienceRecording

Technologies for large scale cortical imaging and electrophysiology

Suhasa Kodandaramaiah
University of Minnesota
Jun 22, 2021

Neural computations occurring simultaneously in multiple cerebral cortical regions are critical for mediating behaviors. Progress has been made in understanding how neural activity in specific cortical regions contributes to behavior. However, there is a lack of tools that allow simultaneous monitoring and perturbing neural activity from multiple cortical regions. We have engineered a suite of technologies to enable easy, robust access to much of the dorsal cortex of mice for optical and electrophysiological recordings. First, I will describe microsurgery robots that can programmed to perform delicate microsurgical procedures such as large bilateral craniotomies across the cortex and skull thinning in a semi-automated fashion. Next, I will describe digitally designed, morphologically realistic, transparent polymer skulls that allow long-term (>300 days) optical access. These polymer skulls allow mesoscopic imaging, as well as cellular and subcellular resolution two-photon imaging of neural structures up to 600 µm deep. We next engineered a widefield, miniaturized, head-mounted fluorescence microscope that is compatible with transparent polymer skull preparations. With a field of view of 8 × 10 mm2 and weighing less than 4 g, the ‘mini-mScope’ can image most of the mouse dorsal cortex with resolutions ranging from 39 to 56 µm. We used the mini-mScope to record mesoscale calcium activity across the dorsal cortex during sensory-evoked stimuli, open field behaviors, social interactions and transitions from wakefulness to sleep.

SeminarNeuroscienceRecording

Assessing and improving vision restoration using ex vivo retina

Günther Zeck
EMCE Institute, TU Wien (Vienna University of Technology)
Jun 22, 2021
SeminarNeuroscienceRecording

GED: A flexible family of versatile methods for hypothesis-driven multivariate decompositions

Mike X Cohen
Donders Centre for Medical Neuroscience
Jun 16, 2021

Does that title put you to sleep or pique your interest? The goal of my presentation is to introduce a powerful yet under-utilized mathematical equation that is surprisingly effective at uncovering spatiotemporal patterns that are embedded in data -- but that might be inaccessible in traditional analysis methods due to low SNR or sparse spatial distribution. If you flunked calculus, then don't worry: the math is really easy, and I'll spend most of the time discussing intuition, simulations, and applications in real data. I will also spend some time in the beginning of the talk providing a bird's-eye-view of the empirical research in my lab, which focuses on mesoscale brain dynamics associated with error monitoring and response competition.

ePosterNeuroscience

Robust multiband drift estimation in electrophysiology data

Charlie Windolf, Angelique C Paulk, Yoav Kfir, Eric Trautmann, Samuel Garcia, Domokos Meszéna, William Munoz, Irene Caprara, Mohsen Jamali, Julien Boussard, Ziv Williams, Sydney Cash, Liam Paninski, Erdem Varol

COSYNE 2023

ePosterNeuroscience

Combining electrophysiology, tissue clearing, and light sheet microscopy for an integrated approach towards brain circuit understanding

Sebastian Böhm, Marta Solano Mateos, James A. Oakes, Saiedeh Saghafi, Christoph F. Fuchssteiner, Thomas Klausberger, Hans-Ulrich Dodt

FENS Forum 2024

ePosterNeuroscience

Evaluating the spread of excitation with different types of optogenetic cochlear stimulation through computer simulations and in vivo electrophysiology

Elisabeth Koert, Jonathan Götz, Bettina Wolf, Tobias Moser

FENS Forum 2024

ePosterNeuroscience

Integrated electrophysiology and fiber photometry examination of the prefrontal cortex in the mouse model of implicit learning

Éva Gulyás, Vivien Pillár, Bálint Király, Franciska Benyó, Annamária Benke, Balázs Hangya

FENS Forum 2024

ePosterNeuroscience

Investigation of GABA transport and the GABA/Na+ relationship in human GAT1 using solid-supported membrane-based electrophysiology

Rocco Zerlotti, Elena Dragicevic, Maria Barthmes, Andre Bazzone

FENS Forum 2024

ePosterNeuroscience

Maternal separation modifies the stress sensitivity, electrophysiology, and morphology of rat nucleus incertus neurons

Anna Gugula, Patryk Sambak, Aleksandra Trenk, Sylwia Drabik, Aleksandra Nogaj, Zbigniew Soltys, Andrew L. Gundlach, Anna Blasiak

FENS Forum 2024

ePosterNeuroscience

MRI-visible superparamagnetic ultraflexible electrodes for precision electrophysiology

Eminhan Ozil, Peter Gombkoto, Tansel Baran Yasar, Angeliki Vavladeli, Markus Marks, Wolfger von der Behrens, Mehmet Fatih Yanik

FENS Forum 2024

ePosterNeuroscience

Navigating through the entorhinal cortex: Combining single-cell electrophysiology and RNA sequencing to advance our knowledge on the neuronal architecture

Eliška Waloschková, Attila Ozsvar, Wen-Hsien Hou, Konstantin Khodosevich, Martin Hemberg, Jan Gorodkin, Stefan Seemann, Vanessa Hall

FENS Forum 2024

ePosterNeuroscience

Next-generation electrophysiology for functional characterization of human neural organoids

Laura D'ignazio, Elvira Guella, Zhuoliang Li, Anastasiia Oryshchuk, Praveena Manogaran, Marie Engelene Obien

FENS Forum 2024

ePosterNeuroscience

Simultaneous calcium imaging and extracellular electrophysiology using CMOS-based imaging devices with an integrated carbon electrode for freely moving mice experiments

Virgil Christian Castillo, Ryoma Okada, Kuang Chih Tso, Yoshinori Sunaga, Yasumi Ohta, Hironari Takehara, Hiroyuki Tashiro, Kiyotaka Sasagawa, Jun Ohta

FENS Forum 2024

ePosterNeuroscience

Streamlining electrophysiology data analysis: A Python-based workflow for efficient integration and processing

Simon Gross, Philipp Janz, Anastasios Moresis, Otto Fajardo, Philipp Schoenenberger, Roger Redondo

FENS Forum 2024

electrophysiology coverage

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