Oligodendrocytes use postsynaptic proteins to coordinate myelin formation on axons of distinct neurotransmitter classes.

bioRxiv

Section of Developmental Biology, Department of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, Colorado, USA, 80445.

Published: November 2024

AI Article Synopsis

  • Axon myelination plays a crucial role in refining neuronal circuits by adjusting myelin sheath patterns across different axon types, but the coordination behind this process is still not fully understood.
  • Recent studies suggest that neuronal activity and the release of vesicles can stimulate the formation of myelin, and oligodendrocytes express proteins that may aid in their interaction with axons for proper myelination.
  • In larval zebrafish, the protein Gephyrin (Gphn) appears to selectively enhance myelin formation on GABAergic axons, with findings showing that in Gphn-deficient larvae, there were longer myelin sheaths on GABAergic axons

Article Abstract

Axon myelination can tune neuronal circuits through placement and modulation of different patterns of myelin sheaths on distinct types of axons. How myelin formation is coordinated on distinct axon classes remains largely unknown. Recent work indicates neuronal activity and vesicle release promote myelin formation, and myelin-producing oligodendrocytes express canonical postsynaptic factors that potentially facilitate oligodendrocyte-axon interaction for myelin ensheathment. Here, we examined whether the inhibitory postsynaptic scaffold protein Gephyrin (Gphn) mediates selective myelination of specific axon classes in the larval zebrafish. Consistent with this possibility, Gphn was enriched in myelin on GABAergic and glycinergic axons. Strikingly, in deficient larvae, myelin sheaths were longer specifically on GABAergic axons, and the frequency of myelin placement shifted toward glutamatergic axons at the expense of GABAergic axons. Collectively, our results indicate that oligodendrocytes use postsynaptic machinery to coordinate myelin formation in an axon identity-dependent manner.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11580840PMC
http://dx.doi.org/10.1101/2024.10.02.616365DOI Listing

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