Signal relay by BMP antagonism controls the SHH/FGF4 feedback loop in vertebrate limb buds

被引:370
作者
Zúniga, A
Haramis, APG
McMahon, AP
Zeller, R
机构
[1] Univ Utrecht, Fac Biol, Dept Dev Biol, NL-3584 CH Utrecht, Netherlands
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
[3] Harvard Univ, Cambridge, MA 02138 USA
关键词
D O I
10.1038/44157
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Outgrowth and patterning of the vertebrate limb are controlled by reciprocal interactions between the posterior mesenchyme (polarizing region) and a specialized ectodermal structure, the apical ectodermal ridge (AER)(1). Sonic hedgehog (SHH) signalling by the polarizing region modulates fibroblast growth factor (FGF)4 signalling by the posterior AER, which in turn maintains the polarizing region (SHH/FGF4 feedback loop)(2,3). Here we report that the secreted bone-morphogenetic-protein (BMP) antagonist Gremlin(4) relays the SHH signal from the polarizing region to the AER. Mesenchymal Gremlin expression is lost in limb buds of mouse embryos homozygous for the limb deformity (Id) mutation, which disrupts establishment of the SHH/FGF4 feedback loop(5-7). Grafting Gremlin-expressing cells into Id mutant limb buds rescues Fgf4 expression and restores the SHH/FGF4 feedback loop. Analysis of Shh-null mutant embryos(8,9) reveals that SHH signalling is required for maintenance of Gremlin and Formin (the gene disrupted by the ld mutations)(10,11). In contrast, Formin, Gremlin and Fgf4 activation are independent of SHH signalling. This study uncovers the cascade by which the SHH signal is relayed from the posterior mesenchyme to the AER and establishes that Formin-dependent activation of the BMP antagonist Gremlin is sufficient to induce Fgf4 and establish the SHH/FGF4 feedback loop.
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页码:598 / 602
页数:5
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