C. elegans MAGU-2/Mpp5 homolog regulates epidermal phagocytosis and synapse density

Salvatore J. Cherra, Alexandr Goncharov, Daniela Boassa, Mark Ellisman, Yishi Jin

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Synapses are dynamic connections that underlie essential functions of the nervous system. The addition, removal, and maintenance of synapses govern the flow of information in neural circuits throughout the lifetime of an animal. While extensive studies have elucidated many intrinsic mechanisms that neurons employ to modulate their connections, increasing evidence supports the roles of non-neuronal cells, such as glia, in synapse maintenance and circuit function. We previously showed that C. elegans epidermis regulates synapses through ZIG-10, a cell-adhesion protein of the immunoglobulin domain superfamily. Here we identified a member of the Pals1/MPP5 family, MAGU-2, that functions in the epidermis to modulate phagocytosis and the number of synapses by regulating ZIG-10 localization. Furthermore, we used light and electron microscopy to show that this epidermal mechanism removes neuronal membranes from the neuromuscular junction, dependent on the conserved phagocytic receptor CED-1. Together, our study shows that C. elegans epidermis constrains synaptic connectivity, in a manner similar to astrocytes and microglia in mammals, allowing optimized output of neural circuits.

Original languageEnglish
Pages (from-to)298-306
Number of pages9
JournalJournal of Neurogenetics
Volume34
Issue number3-4
DOIs
StatePublished - 2020

Bibliographical note

Publisher Copyright:
© 2020 Informa UK Limited, trading as Taylor & Francis Group.

Funding

Some strains were provided by National BioResource Project (Dr. S. Mitani) and the Caenorhabditis Genetics Center, which is funded by the National Institutes of Health Office of Research Infrastructure Programs [P40-OD010440]. The electron micrographs were taken in the UCSD Cellular and Molecular Medicine Electron microscopy core facility, which is supported in part by National Institutes of Health Award [S10-OD023527]. This work was supported by grants from the National Institutes of Health to S.J.C. [K99-NS097638], D.B. [R01-GM086197], M.E. [P41-GM103412], and Y.J. [R01 and R37-NS035546]. We thank the members of the Jin laboratory for constructive comments. We thank J.S. Dittman for reporter lines. We appreciate Wormbase for genetic and genomic information.

FundersFunder number
National Institutes of Health (NIH)R01, R37-NS035546, S10-OD023527, R01-GM086197, K99-NS097638, P41-GM103412
National Institutes of Health (NIH)
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical SciencesR24GM137200
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical Sciences
Office of Research Infrastructure Programs, National Institutes of HealthP40-OD010440
Office of Research Infrastructure Programs, National Institutes of Health

    Keywords

    • ACR-2
    • MAGUK
    • glia
    • miniSOG
    • neuromuscular junction
    • synapse elimination

    ASJC Scopus subject areas

    • Genetics
    • Cellular and Molecular Neuroscience

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