Synaptotagmin-3 drives AMPA receptor endocytosis, depression of synapse strength, and forgetting

Author:

Awasthi Ankit1ORCID,Ramachandran Binu1,Ahmed Saheeb1,Benito Eva23,Shinoda Yo1ORCID,Nitzan Noam1ORCID,Heukamp Alina1ORCID,Rannio Sabine1,Martens Henrik4,Barth Jonas23ORCID,Burk Katja1ORCID,Wang Yu Tian5ORCID,Fischer Andre23,Dean Camin1ORCID

Affiliation:

1. Trans-synaptic Signaling Group, European Neuroscience Institute, 37077 Goettingen, Germany.

2. German Center for Neurodegenerative Disease, 37075 Goettingen, Germany.

3. Department of Psychiatry and Psychotherapy, University Medical Center Goettingen, 37075 Goettingen, Germany.

4. Synaptic Systems GmbH, 37079 Goettingen, Germany.

5. Brain Research Center and Department of Medicine, University of British Columbia, Vancouver, BC V6T2B5, Canada.

Abstract

Forgetting and receptor removal The trafficking of AMPA receptors to and from the surface of postsynaptic membranes regulates synaptic strength and underlies learning and memory. Awasthi et al. found that the integral membrane protein synaptotagmin-3 (Syt3) is predominantly found on postsynaptic endocytic zones of neurons, where it promotes AMPA receptor internalization (see the Perspective by Mandelberg and Tsien). In Syt3 overexpressing or knockdown neurons, synaptic transmission and short-term plasticity were unchanged. However, in neurons from Syt3 knockout mice, synaptic long-term depression was abolished and decaying long-term potentiation endured. In Syt3 knockout mice, spatial learning was unaltered; however, these animals showed signs of impaired forgetting and relearning during the water maze spatial memory task. Science , this issue p. eaav1483 ; see also p. 31

Funder

Alexander von Humboldt-Stiftung

FP7 Ideas: European Research Council

Deutsche Forschungsgemeinschaft

Canadian Institute for Health Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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