Transsynaptic cerebellin 4–neogenin 1 signaling mediates LTP in the mouse dentate gyrus

Author:

Liakath-Ali Kif12,Polepalli Jai S.123,Lee Sung-Jin12,Cloutier Jean-Francois45,Südhof Thomas C.12

Affiliation:

1. Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305

2. HHMI, Stanford University, Stanford, CA 94305

3. Healthy Longevity Translational Research Program, Department of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 119077

4. Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University, Montreal, QC H3A 2B4, Canada

5. Department of Anatomy and Cell Biology, McGill University, Montreal, QC H3A 0C7, Canada

Abstract

Significance Synapses are controlled by transsynaptic adhesion complexes that mediate bidirectional signaling between pre- and postsynaptic compartments. Long-term potentiation (LTP) of synaptic transmission is thought to enable synaptic modifications during memory formation, but the signaling mechanisms involved remain poorly understood. We show that binding of cerebellin-4 (Cbln4), a secreted ligand of presynaptic neurexin adhesion molecules, to neogenin-1, a postsynaptic surface protein known as a developmental netrin receptor, is essential for normal LTP at entorhinal cortex→dentate gyrus synapses in mice. Cbln4 and neogenin-1 are dispensable for basal synaptic transmission and not involved in establishing synaptic connections as such. Our data identify a netrin receptor as a postsynaptic organizer of synaptic plasticity that collaborates specifically with the presynaptic neurexin–ligand Cbln4.

Funder

HHS | NIH | National Institute of Mental Health

European Molecular Biology Organization

Larry L. Hillblom Foundation

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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