Postsynaptic receptors regulate presynaptic transmitter stability through transsynaptic bridges

Author:

Godavarthi Swetha K.12,Hiramoto Masaki3ORCID,Ignatyev Yuri4,Levin Jacqueline B.5,Li Hui-quan12,Pratelli Marta12ORCID,Borchardt Jennifer6ORCID,Czajkowski Cynthia6,Borodinsky Laura N.5,Sweeney Lora4,Cline Hollis T.3,Spitzer Nicholas C.12ORCID

Affiliation:

1. Neurobiology Department, University of California San Diego, La Jolla, CA 92093

2. Kavli Institute for Brain & Mind, University of California San Diego, La Jolla, CA 92093

3. Neuroscience Department, The Scripps Research Institute, La Jolla, CA 92037

4. Institute of Science and Technology Austria, Klosterneuburg 3400, Austria

5. Department of Physiology & Membrane Biology Shriners Hospital for Children Northern California, University of California Davis School of Medicine, Sacramento, CA 95817

6. Neuroscience Department, University of Wisconsin Madison, Madison, WI 53705

Abstract

Stable matching of neurotransmitters with their receptors is fundamental to synapse function and reliable communication in neural circuits. Presynaptic neurotransmitters regulate the stabilization of postsynaptic transmitter receptors. Whether postsynaptic receptors regulate stabilization of presynaptic transmitters has received less attention. Here, we show that blockade of endogenous postsynaptic acetylcholine receptors (AChR) at the neuromuscular junction destabilizes the cholinergic phenotype in motor neurons and stabilizes an earlier, developmentally transient glutamatergic phenotype. Further, expression of exogenous postsynaptic gamma-aminobutyric acid type A receptors (GABA A receptors) in muscle cells stabilizes an earlier, developmentally transient GABAergic motor neuron phenotype. Both AChR and GABA A receptors are linked to presynaptic neurons through transsynaptic bridges. Knockdown of specific components of these transsynaptic bridges prevents stabilization of the cholinergic or GABAergic phenotypes. Bidirectional communication can enforce a match between transmitter and receptor and ensure the fidelity of synaptic transmission. Our findings suggest a potential role of dysfunctional transmitter receptors in neurological disorders that involve the loss of the presynaptic transmitter.

Funder

National Science Foundation

Overland Foundation

Publisher

Proceedings of the National Academy of Sciences

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