Perinatal Institute, Cincinnati Children's Research Foundation, Cincinnati, OH 45229, USA.
Dev Cell. 2012 Aug 14;23(2):292-304. doi: 10.1016/j.devcel.2012.07.002. Epub 2012 Aug 2.
The liver, pancreas, and lungs are induced from endoderm progenitors by a series of dynamic growth factor signals from the mesoderm, but how the temporal-spatial activity of these signals is controlled is poorly understood. We have identified an extracellular regulatory loop required for robust bone morphogenetic protein (BMP) signaling in the Xenopus foregut. We show that BMP signaling is required to maintain foregut progenitors and induce expression of the secreted frizzled related protein Sizzled (Szl) and the extracellular metalloprotease Tolloid-like 1 (Tll1). Szl negatively regulates Tll activity to control deposition of a fibronectin (FN) matrix between the mesoderm and endoderm, which is required to maintain BMP signaling. Foregut-specific Szl depletion results in a loss of the FN matrix and failure to maintain robust pSmad1 levels, causing a loss of foregut gene expression and organ agenesis. These results have implications for BMP signaling in diverse contexts and the differentiation of foregut tissue from stem cells.
肝脏、胰腺和肺由中胚层来源的一系列动态生长因子信号诱导而来,这些信号的时空活性如何调控还知之甚少。我们已经鉴定出一个在非洲爪蟾前肠中维持骨形态发生蛋白(BMP)信号所必需的细胞外调节环。我们发现 BMP 信号对于维持前肠祖细胞并诱导分泌卷曲相关蛋白(Sizzled,Szl)和细胞外金属蛋白酶 Tolloid-like 1(Tolloid-like 1,Tll1)的表达是必需的。Szl 负调控 Tll 的活性以控制中胚层和内胚层之间纤维连接蛋白(fibronectin,FN)基质的沉积,这对于维持 BMP 信号是必需的。前肠特异性 Szl 耗竭导致 FN 基质的丧失和无法维持强壮的 pSmad1 水平,导致前肠基因表达和器官发生缺失。这些结果对不同背景下的 BMP 信号和干细胞分化为前肠组织具有重要意义。