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Differential Inhibition of Sox10 Functions by Notch-Hes Pathway
- Source :
- Cellular and Molecular Neurobiology. 40:653-662
- Publication Year :
- 2019
- Publisher :
- Springer Science and Business Media LLC, 2019.
-
Abstract
- In the developing central nervous system, the terminal differentiation of oligodendrocytes (OLs) is regulated by both extrinsic and intrinsic factors. Recent studies have suggested that the Notch-Hes signaling pathway influences the maturation of oligodendrocytes in culture and during development. However, the specific Notch receptors and their downstream effectors Hes genes that are involved in oligodendrocyte maturation have not been investigated systematically. In this study, we showed that Notch1 and Notch3 are expressed in oligodendrocyte precursor cells (OPCs) during gliogenesis, and Hes5 is the major Notch downstream transcription factor that is transiently expressed in OPCs. Overexpression of Notch intracellular domain (NICD) and Hes5 proteins in embryonic chicken spinal cord suppressed both the endogenous and Sox10-induced Mbp gene expression. Unexpectedly, overexpression of NICD/Hes5 did not inhibit Sox10 induction of Olig2 expression and Myrf induced Mbp expression, suggesting the differential inhibitory effects of NICD/Hes5 signaling on Sox10 activation of myelin-related genes and early progenitor genes.
- Subjects :
- 0301 basic medicine
SOX10
HES5
Biology
OLIG2
03 medical and health sciences
Cellular and Molecular Neuroscience
0302 clinical medicine
Gene expression
Basic Helix-Loop-Helix Transcription Factors
medicine
Animals
Transcription factor
Gliogenesis
Mice, Knockout
Receptors, Notch
SOXE Transcription Factors
Stem Cells
Gene Expression Regulation, Developmental
Myelin Basic Protein
Cell Biology
General Medicine
Oligodendrocyte
Cell biology
Oligodendroglia
030104 developmental biology
medicine.anatomical_structure
Spinal Cord
embryonic structures
Signal transduction
Chickens
030217 neurology & neurosurgery
Signal Transduction
Subjects
Details
- ISSN :
- 15736830 and 02724340
- Volume :
- 40
- Database :
- OpenAIRE
- Journal :
- Cellular and Molecular Neurobiology
- Accession number :
- edsair.doi.dedup.....6678c0306cae93f82adcde9f652a240c