Cooperation between sonic hedgehog and fibroblast growth factor/MAPK signalling pathways in neocortical precursors

被引:112
作者
Kessaris, N
Jamen, F
Rubin, LL
Richardson, WD
机构
[1] UCL, Wolfson Inst Biomed Res, London, England
[2] UCL, Dept Biol, London, England
[3] Curis, Cambridge, MA 02138 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 06期
关键词
FGF; SHH; MAPK; embryonic neural stem cells; cell fate specification; neural development; oligodendrocyte progenitors; mouse;
D O I
10.1242/dev.01027
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sonic hedgehog (SHH) and fibroblast growth factor 2 (FGF2) can both induce neocortical precursors to express the transcription factor OLIG2 and generate oligodendrocyte progenitors (OLPs) in culture. The activity of FGF2 is unaffected by cyclopamine, which blocks Hedgehog signalling, demonstrating that the FGF pathway to OLP production is Hedgehog independent. Unexpectedly, SHH-mediated OLP induction is blocked by PD173074, a selective inhibitor of FGF receptor (FGFR) tyrosine kinase. SHH activity also depends on mitogen-activated protein kinase (MAPK) but SHH does not itself activate MAPK. Instead, constitutive activity of FGFR maintains a basal level of phosphorylated MAPK that is absolutely required for the OLIG2- and OLP-inducing activities of SHH. Stimulating the MAPK pathway with a retrovirus encoding constitutively active RAS shows that the requirement for MAPK is cell-autonomous, i.e. MAPK is needed together with SHH signalling in the cells that become OLPs.
引用
收藏
页码:1289 / 1298
页数:10
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