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High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling

Ensheathment of axons by myelin is a highly complex and multi-cellular process. Cytosolic calcium (Ca(2+)) changes in the myelin sheath have been implicated in myelin synthesis, but the source of this Ca(2+) and the role of neuronal activity is not well understood. Using one-photon Ca(2+) imaging, w...

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Detalles Bibliográficos
Autores principales: Battefeld, Arne, Popovic, Marko A., de Vries, Sharon I., Kole, Maarten H.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316190/
https://www.ncbi.nlm.nih.gov/pubmed/30605675
http://dx.doi.org/10.1016/j.celrep.2018.12.039
Descripción
Sumario:Ensheathment of axons by myelin is a highly complex and multi-cellular process. Cytosolic calcium (Ca(2+)) changes in the myelin sheath have been implicated in myelin synthesis, but the source of this Ca(2+) and the role of neuronal activity is not well understood. Using one-photon Ca(2+) imaging, we investigated myelin sheath formation in the mouse somatosensory cortex and found a high rate of spontaneous microdomain Ca(2+) transients and large-amplitude Ca(2+) waves propagating along the internode. The frequency of Ca(2+) transients and waves rapidly declines with maturation and reactivates during remyelination. Unexpectedly, myelin microdomain Ca(2+) transients occur independent of neuronal action potential generation or network activity but are nearly completely abolished when the mitochondrial permeability transition pores are blocked. These findings are supported by the discovery of mitochondria organelles in non-compacted myelin. Together, the results suggest that myelin microdomain Ca(2+) signals are cell-autonomously driven by high activity of mitochondria during myelin remodeling.