The WNT antagonist cSFRP2 modulates programmed cell death in the developing hindbrain

被引:0
作者
Ellies, DL
Church, V
Francis-West, P
Lumsden, A
机构
[1] Kings Coll London, MRC, Ctr Dev Neurobiol, London SE1 1UL, England
[2] Kings Coll London, Dept Cranofacial Dev, London SE1 1UL, England
来源
DEVELOPMENT | 2000年 / 127卷 / 24期
关键词
neural crest cell; programmed cell death; Wnt; chick;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the avian hindbrain, the loss of premigratory neural crest cells from rhombomeres 3 and 5 (r3, r5) through programmed cell death contributes to the patterning of emigrant crest cells into three discrete streams. Programmed cell death is induced by the upregulation of Bmp4 and Msx2 in r3 and r5. We show that cSFRP2, a WNT antagonist, is expressed in the even-numbered rhombomeres and that over-expression of cSfrp2 inhibits Bmp4 expression in r3 and r5, preventing programmed cell death. By contrast, depleting cSFRP2 function in r4 results in elevated levels of Msx2 expression and ectopic programmed cell death, as does overexpression of Wnt1. We propose that programmed cell death in the rhombencephalic neural crest is modulated by pre-patterned cSfrp2 expression and a WNT-BMP signalling loop.
引用
收藏
页码:5285 / 5295
页数:11
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