Table of Contents

Electrophysiological Signatures of Visual Recognition Memory across All Layers of Mouse V1

  1. Mark F. Bear1
  1. 1The Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
  2. 2Biochemistry Program, Wellesley College, Wellesley, Massachusetts 02481
  1. Author contributions: D.J.H., P.S.B.F., A.T., S.F.C., and M.F.B. designed research; D.J.H., P.S.B.F., A.T., A.Y.L., and S.F.C. performed research; D.J.H., P.S.B.F., and S.F.C. analyzed data; D.J.H., P.S.B.F., and S.F.C. wrote the first draft of the paper; D.J.H., P.S.B.F., A.T., S.F.C., and M.F.B. edited the paper; M.F.B. wrote the paper.

  2. ↵*D.J.H. and P.S.B.F. contributed equally to this work.

  • D.J. Hayden's present address: Kavli Institute for Systems Neuroscience and Centre for Neural Computation, Norwegian University of Science and Technology, Trondheim 7020, Norway.

  • P.S.B. Finnie's present address: Department of Pharmacology and Toxicology, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

  • A. Thomazeau's present address: Brain Repair and Integrative Neuroscience Program, Centre for Research in Neuroscience, Departments of Medicine, and Neurology & Neurosurgery, The Research Institute of the McGill University Health Centre, Montreal General Hospital, Montreal, Quebec H3G 1A4, Canada.

  • A.Y. Li's present address: Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Ontario M5S 1A8, Canada.

  • S.F. Cooke's present address: The Medical Research Council Centre for Neurodevelopmental Disorders (MRC CNDD) and Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London SE5 8AF, United Kingdom.

Abstract

In mouse primary visual cortex (V1), familiar stimuli evoke significantly altered responses when compared with novel stimuli. This stimulus-selective response plasticity (SRP) was described originally as an increase in the magnitude of visual evoked potentials (VEPs) elicited in layer 4 (L4) by familiar phase-reversing grating stimuli. SRP is dependent on NMDA receptors (NMDARs) and has been hypothesized to reflect potentiation of thalamocortical (TC) synapses in L4. However, recent evidence indicates that the synaptic modifications that manifest as SRP do not occur on L4 principal cells. To shed light on where and how SRP is induced and expressed in male and female mice, the present study had three related aims: (1) to confirm that NMDAR are required specifically in glutamatergic principal neurons of V1, (2) to investigate the consequences of deleting NMDAR specifically in L6, and (3) to use translaminar electrophysiological recordings to characterize SRP expression in different layers of V1. We find that knock-out (KO) of NMDAR in L6 principal neurons disrupts SRP. Current-source density (CSD) analysis of the VEP depth profile shows augmentation of short latency current sinks in layers 3, 4, and 6 in response to phase reversals of familiar stimuli. Multiunit recordings demonstrate that increased peak firing occurs in response to phase reversals of familiar stimuli across all layers, but that activity between phase reversals is suppressed. Together, these data reveal important aspects of the underlying phenomenology of SRP and generate new hypotheses for the expression of experience-dependent plasticity in V1.

SIGNIFICANCE STATEMENT Repeated exposure to stimuli that portend neither reward nor punishment leads to behavioral habituation, enabling organisms to dedicate attention to novel or otherwise significant features of the environment. The neural basis of this process, which is so often dysregulated in neurologic and psychiatric disorders, remains poorly understood. Learning and memory of stimulus familiarity can be studied in mouse visual cortex by measuring electrophysiological responses to simple phase-reversing grating stimuli. The current study advances knowledge of this process by documenting changes in visual evoked potentials (VEPs), neuronal spiking activity, and oscillations in the local field potentials (LFPs) across all layers of mouse visual cortex. In addition, we identify a key contribution of a specific population of neurons in layer 6 (L6) of visual cortex.

  • Received January 16, 2023.
  • Revision received August 31, 2023.
  • Accepted September 5, 2023.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

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