Oligodendroglial primary cilium heterogeneity during development and demyelination/remyelination
The primary cilium (PC) has emerged as an indispensable cellular antenna essential for signal transduction of important cell signaling pathways. The rapid acquisition of knowledge about PC biology has raised attention to PC as a therapeutic target in some neurological and psychiatric diseases. Howev...
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Published in: | Frontiers in cellular neuroscience Vol. 16; p. 1049468 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
Frontiers Research Foundation
24-11-2022
Frontiers Media S.A |
Subjects: | |
Online Access: | Get full text |
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Summary: | The primary cilium (PC) has emerged as an indispensable cellular antenna essential for signal transduction of important cell signaling pathways. The rapid acquisition of knowledge about PC biology has raised attention to PC as a therapeutic target in some neurological and psychiatric diseases. However, the role of PC in oligodendrocytes and its participation in myelination/remyelination remain poorly understood. Oligodendrocyte precursor cells (OPCs) give rise to oligodendrocytes during central nervous system (CNS) development. In adult, a small percentage of OPCs remains as undifferentiated cells located sparsely in the different regions of the CNS. These cells can regenerate oligodendrocytes and participate to certain extent in remyelination. This study aims characterize PC in oligodendrocyte lineage cells during post-natal development and in a mouse model of demyelination/remyelination. We show heterogeneity in the frequency of cilium presence on OPCs, depending on culture conditions
and cerebral regions
during development and demyelination/remyelination.
, Lithium chloride (LiCl), Forskolin and Chloral Hydrate differentially affect cilium, depending on culture environment and PC length correlates with the cell differentiation state. Beside the role of PC as a keeper of cell proliferation, our results suggest its involvement in myelination/remyelination. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Hiroaki Wake, Nagoya University, Japan Reviewed by: Holly Colognato, Stony Brook University, United States; Enrica Boda, University of Turin, Italy This article was submitted to Non-Neuronal Cells, a section of the journal Frontiers in Cellular Neuroscience |
ISSN: | 1662-5102 1662-5102 |
DOI: | 10.3389/fncel.2022.1049468 |