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Author Notes:

james.zheng@emory.edu

Y.R. and J.Q.Z. designed research; Y.R. and S.L.P. performed research; Y.R., S.L.P., K.R.M., and J.Q.Z. analyzed data; Y.R., S.L.P., K.R.M., Y.F., and J.Q.Z. wrote the paper.

The authors declare no competing financial interests.

Subjects:

Research Funding:

This work was supported in part by National Institutes of Health Grants MH104632 and MH108025 (to J.Q.Z.) and NS110110 (to Y.F.), the Ruth L. Kirschstein National Research Service Award Postdoctoral Fellowship NS092342 (to K.R.M.), and the Emory University Integrated Cellular Imaging Microscopy Core of the Emory Neuroscience National Institute of Neurological Disorders and Stroke Core Facilities Grant 5P30NS055077. This work was also supported in part by the Emory University Integrated Cellular Imaging Core and a pilot grant from the Core.

Keywords:

  • Ca2+ signaling
  • internal Ca2+ stores
  • oligodendrocytes
  • store-operated Ca2+ entry

Spontaneous local calcium transients regulate oligodendrocyte development in culture through store-operated Ca^2+ entry and release

Tools:

Journal Title:

eNeuro

Volume:

Volume 7, Number 4

Publisher:

, Pages 1-16

Type of Work:

Article | Final Publisher PDF

Abstract:

Oligodendrocytes (OLs) insulate axonal fibers for fast conduction of nerve impulses by wrapping axons of the CNS with compact myelin membranes. Differentiating OLs undergo drastic chances in cell morphology. Bipolar oligodendroglial precursor cells (OPCs) transform into highly ramified multipolar OLs, which then ex-pand myelin membranes that enwrap axons. While significant progress has been made in understanding the molecular and genetic mechanisms underlying CNS myelination and its disruption in diseases, the cellular mechanisms that regulate OL differentiation are not fully understood. Here, we report that developing rat OLs in culture exhibit spontaneous Ca local transients (sCaLTs) in their process arbors in the absence of neurons. Importantly, we find that the frequency of sCaLTs markedly increases as OLs undergo extensive process outgrowth and branching. We further show that sCaLTs are primarily generated through a combination of Ca influx through store-operated Ca entry (SOCE) and Ca release from internal Ca stores. Inhibition of sCaLTs impairs the elaboration and branching of OL processes, as well as substantially reduces the formation of large myelin sheets in culture. Together, our findings identify an important role for spontaneous local Ca signaling in OL development. 2+ 2+ 2+ 2+ 2+ 2+

Copyright information:

© 2020 Rui et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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