Notch1 control of oligodendrocyte differentiation in the spinal cord.


Autoria(s): Genoud S.; Lappe-Siefke C.; Goebbels S.; Radtke F.; Aguet M.; Scherer S.S.; Suter U.; Nave K.A.; Mantei N.
Data(s)

2002

Resumo

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.

Identificador

https://serval.unil.ch/?id=serval:BIB_27E702FE5FB7

isbn:0021-9525

pmid:12186854

doi:10.1083/jcb.200202002

isiid:000177649900011

http://my.unil.ch/serval/document/BIB_27E702FE5FB7.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_27E702FE5FB76

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

The Journal of cell biology, vol. 158, no. 4, pp. 709-18

Palavras-Chave #Animals; Apoptosis; Cell Differentiation; Membrane Proteins; Mice; Mice, Transgenic; Mutation; Oligodendroglia; Prosencephalon; Receptor, Notch1; Receptors, Cell Surface; Spinal Cord; Transcription Factors
Tipo

info:eu-repo/semantics/article

article