Notch1 control of oligodendrocyte differentiation in the spinal cord
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Open Access
- 19 August 2002
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 158 (4) , 709-718
- https://doi.org/10.1083/jcb.200202002
Abstract
We have selectively inhibited Notch1 signaling in oligodendrocyte precursors (OPCs) using the Cre/loxP system in transgenic mice to investigate the role of Notch1 in oligodendrocyte (OL) development and differentiation. Early development of OPCs appeared normal in the spinal cord. However, at embryonic day 17.5, premature OL differentiation was observed and ectopic immature OLs were present in the gray matter. At birth, OL apoptosis was strongly increased in Notch1 mutant animals. Premature OL differentiation was also observed in the cerebrum, indicating that Notch1 is required for the correct spatial and temporal regulation of OL differentiation in various regions of the central nervous system. These findings establish a widespread function of Notch1 in the late steps of mammalian OPC development in vivo.Keywords
This publication has 83 references indexed in Scilit:
- Autonomous and non-autonomous regulation of mammalian neurite development by Notch1 and Delta1Current Biology, 1999
- Single or multiple oligodendroglial lineages: A controversyGlia, 1999
- From Neural Stem Cells to Myelinating OligodendrocytesMolecular and Cellular Neuroscience, 1999
- Contact-Dependent Inhibition of Cortical Neurite Growth Mediated by Notch SignalingScience, 1999
- Notch Signaling: Cell Fate Control and Signal Integration in DevelopmentScience, 1999
- Pax6 Influences the Time and Site of Origin of Glial Precursors in the Ventral Neural TubeMolecular and Cellular Neuroscience, 1998
- Four-kilobase sequence of the mouse CNP gene directs spatial and temporal expression of lacZ in transgenic miceJournal of Neuroscience Research, 1998
- PEST sequences and regulation by proteolysisTrends in Biochemical Sciences, 1996
- Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation.The Journal of cell biology, 1992