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High-Frequency Microdomain Ca2+ Transients and Waves during Early Myelin Internode Remodeling.
Battefeld, Arne; Popovic, Marko A; de Vries, Sharon I; Kole, Maarten H P.
Affiliation
  • Battefeld A; Department of Axonal Signaling, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA, Amsterdam, the Netherlands. Electronic address: arne.battefeld@u-bordeaux.fr.
  • Popovic MA; Department of Axonal Signaling, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA, Amsterdam, the Netherlands.
  • de Vries SI; Department of Axonal Signaling, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA, Amsterdam, the Netherlands.
  • Kole MHP; Department of Axonal Signaling, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA, Amsterdam, the Netherlands; Cell Biology, Faculty of Science, University of Utrecht, Padualaan 8, 3584 CH, Utrecht, the Netherlands. Electronic address: m
Cell Rep ; 26(1): 182-191.e5, 2019 01 02.
Article in En | MEDLINE | ID: mdl-30605675
ABSTRACT
Ensheathment of axons by myelin is a highly complex and multi-cellular process. Cytosolic calcium (Ca2+) changes in the myelin sheath have been implicated in myelin synthesis, but the source of this Ca2+ and the role of neuronal activity is not well understood. Using one-photon Ca2+ imaging, we investigated myelin sheath formation in the mouse somatosensory cortex and found a high rate of spontaneous microdomain Ca2+ transients and large-amplitude Ca2+ waves propagating along the internode. The frequency of Ca2+ transients and waves rapidly declines with maturation and reactivates during remyelination. Unexpectedly, myelin microdomain Ca2+ 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 Ca2+ signals are cell-autonomously driven by high activity of mitochondria during myelin remodeling.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium / Myelin Sheath Limits: Animals Language: En Journal: Cell Rep Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium / Myelin Sheath Limits: Animals Language: En Journal: Cell Rep Year: 2019 Document type: Article