Glia actively sculpt sensory neurons by controlled phagocytosis to tune animal behavior

Author:

Raiders Stephan12ORCID,Black Erik Calvin1,Bae Andrea34,MacFarlane Stephen5,Klein Mason5ORCID,Shaham Shai3ORCID,Singhvi Aakanksha1267ORCID

Affiliation:

1. Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, United States

2. Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, United States

3. Laboratory of Developmental Genetics, The Rockefeller University, New York, United States

4. Cellular Imaging Shared Resources, Fred Hutchinson Cancer Research Center, Seattle, United States

5. Department of Physics and Department of Biology, University of Miami, Coral Gables, United States

6. Department of Biological Structure, University of Washington School of Medicine, Seattle, United States

7. Brotman Baty Institute for Precision Medicine, Seattle, United States

Abstract

Glia in the central nervous system engulf neuron fragments to remodel synapses and recycle photoreceptor outer segments. Whether glia passively clear shed neuronal debris or actively prune neuron fragments is unknown. How pruning of single-neuron endings impacts animal behavior is also unclear. Here, we report our discovery of glia-directed neuron pruning in Caenorhabditis elegans. Adult C. elegans AMsh glia engulf sensory endings of the AFD thermosensory neuron by repurposing components of the conserved apoptotic corpse phagocytosis machinery. The phosphatidylserine (PS) flippase TAT-1/ATP8A functions with glial PS-receptor PSR-1/PSR and PAT-2/α-integrin to initiate engulfment. This activates glial CED-10/Rac1 GTPase through the ternary GEF complex of CED-2/CrkII, CED-5/DOCK180, CED-12/ELMO. Execution of phagocytosis uses the actin-remodeler WSP-1/nWASp. This process dynamically tracks AFD activity and is regulated by temperature, the AFD sensory input. Importantly, glial CED-10 levels regulate engulfment rates downstream of neuron activity, and engulfment-defective mutants exhibit altered AFD-ending shape and thermosensory behavior. Our findings reveal a molecular pathway underlying glia-dependent engulfment in a peripheral sense-organ and demonstrate that glia actively engulf neuron fragments, with profound consequences on neuron shape and animal sensory behavior.

Funder

Simons Foundation

American Federation for Aging Research

NIH Office of the Director

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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