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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
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author Battefeld, Arne
Popovic, Marko A.
de Vries, Sharon I.
Kole, Maarten H.P.
author_facet Battefeld, Arne
Popovic, Marko A.
de Vries, Sharon I.
Kole, Maarten H.P.
author_sort Battefeld, Arne
collection PubMed
description 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.
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spelling pubmed-63161902019-01-08 High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling Battefeld, Arne Popovic, Marko A. de Vries, Sharon I. Kole, Maarten H.P. Cell Rep Article 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. Cell Press 2019-01-02 /pmc/articles/PMC6316190/ /pubmed/30605675 http://dx.doi.org/10.1016/j.celrep.2018.12.039 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Battefeld, Arne
Popovic, Marko A.
de Vries, Sharon I.
Kole, Maarten H.P.
High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling
title High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling
title_full High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling
title_fullStr High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling
title_full_unstemmed High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling
title_short High-Frequency Microdomain Ca(2+) Transients and Waves during Early Myelin Internode Remodeling
title_sort high-frequency microdomain ca(2+) transients and waves during early myelin internode remodeling
topic Article
url 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
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