Regulation by members of the transforming growth factor beta superfamily of the digital and interdigital fates of the autopodial limb mesoderm

被引:31
作者
Macias, D
Gañan, Z
Rodriguez-Leon, J
Merino, R
Hurle, JH
机构
[1] Univ Cantabria, Fac Med, Dept Anat & Cellular Biol, E-39011 Santander, Spain
[2] Univ Extremadura, Dept Ciencias Morfol & Biol Anim & Celular, E-06071 Badajoz, Spain
关键词
apoptosis; chondrogenesis; BMP-receptor; noggin; BMPs; TGF beta s; FGFs;
D O I
10.1007/s004410051270
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonic limb outgrowth is accomplished by the proliferation of mesodermal cells in the progress zone. In this region, mesodermal cells are maintained in an undifferentiated and proliferating state by the action of the apical ectodermal ridge (AER). Differentiation of these cells into individual skeletal elements occurs when the cells are displaced proximally and leave the influence of the AER as a consequence of the accumulation of cells in that region. Here we review the evidence obtained in the last few years showing that members of the transforming growth factor beta (TGF beta) subfamily and bone morphogenetic proteins (BMPs) act as proximal signals in the autopod regulating the fate of the progress zone cells towards chondrogenesis or apoptosis. Our findings show that apoptosis is regulated by BMPs while chondrogenesis requires the interaction of TGF beta s and BMPs. Fibroblast growth factors (FGFs) produced by the AER exert an opposite function to both TGF beta s and BMPs, maintaining the progress zone cells in an undifferentiated state.
引用
收藏
页码:95 / 102
页数:8
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