Cotton Jennifer L, Li Qi, Ma Lifang, Park Joo-Seop, Wang Jiayi, Ou Jianhong, Zhu Lihua J, Ip Y Tony, Johnson Randy L, Mao Junhao
Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Dev Cell. 2017 Oct 9;43(1):35-47.e4. doi: 10.1016/j.devcel.2017.08.019. Epub 2017 Sep 21.
YAP/TAZ are the major mediators of mammalian Hippo signaling; however, their precise function in the gastrointestinal tract remains poorly understood. Here we dissect the distinct roles of YAP/TAZ in endodermal epithelium and mesenchyme and find that, although dispensable for gastrointestinal epithelial development and homeostasis, YAP/TAZ function as the critical molecular switch to coordinate growth and patterning in gut mesenchyme. Our genetic analyses reveal that Lats1/2 kinases suppress expansion of the primitive mesenchymal progenitors, where YAP activation also prevents induction of the smooth muscle lineage through transcriptional repression of Myocardin. During later development, zone-restricted downregulation of YAP/TAZ provides the positional cue and allows smooth muscle cell differentiation induced by Hedgehog signaling. Taken together, our studies identify the mesenchymal requirement of YAP/TAZ in the gastrointestinal tract and highlight the functional interplays between Hippo and Hedgehog signaling underlying temporal and spatial control of tissue growth and specification in developing gut.
YAP/TAZ是哺乳动物Hippo信号通路的主要介导因子;然而,它们在胃肠道中的具体功能仍知之甚少。在这里,我们剖析了YAP/TAZ在内胚层上皮和间充质中的不同作用,发现尽管YAP/TAZ对胃肠道上皮发育和稳态并非必需,但它们作为关键的分子开关来协调肠道间充质的生长和模式形成。我们的遗传学分析表明,Lats1/2激酶抑制原始间充质祖细胞的扩增,YAP激活也通过转录抑制心肌素阻止平滑肌谱系的诱导。在后期发育过程中,YAP/TAZ的区域限制性下调提供了位置线索,并允许由Hedgehog信号诱导的平滑肌细胞分化。综上所述,我们的研究确定了YAP/TAZ在胃肠道中间充质的需求,并突出了Hippo信号通路和Hedgehog信号通路在发育中的肠道组织生长和特化的时空控制中的功能相互作用。