PUBLICATION
Met is required for oligodendrocyte progenitor cell migration in Danio rerio
- Authors
- Ali, M.F., Latimer, A.J., Wang, Y., Hogenmiller, L., Fontenas, L., Isabella, A.J., Moens, C.B., Yu, G., Kucenas, S.
- ID
- ZDB-PUB-210928-12
- Date
- 2021
- Source
- G3 (Bethesda) 11(10): (Journal)
- Registered Authors
- Ali, Maria, Fontenas, Laura, Kucenas, Sarah, Latimer, Andrew, Moens, Cecilia
- Keywords
- Met receptor, glial migration, oligodendrocyte progenitor cells, spinal cord development, zebrafish
- MeSH Terms
-
- Signal Transduction
- Spinal Cord
- Oligodendroglia
- Zebrafish
- Animals
- Cell Differentiation
- Oligodendrocyte Precursor Cells*
- PubMed
- 34568921 Full text @ G3 (Bethesda)
Citation
Ali, M.F., Latimer, A.J., Wang, Y., Hogenmiller, L., Fontenas, L., Isabella, A.J., Moens, C.B., Yu, G., Kucenas, S. (2021) Met is required for oligodendrocyte progenitor cell migration in Danio rerio. G3 (Bethesda). 11(10):.
Abstract
During vertebrate central nervous system development, most oligodendrocyte progenitor cells (OPCs) are specified in the ventral spinal cord and must migrate throughout the neural tube until they become evenly distributed, occupying non-overlapping domains. While this process of developmental OPC migration is well characterized, the nature of the molecular mediators that govern it remain largely unknown. Here, using zebrafish as a model, we demonstrate that Met signaling is required for initial developmental migration of OPCs, and, using cell-specific knock-down of Met signaling, show that Met acts cell-autonomously in OPCs. Taken together, these findings demonstrate in vivo, the role of Met signaling in OPC migration and provide new insight into how OPC migration is regulated during development.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping