Fallah Sepideh, Beaulieu Jean-François
Laboratory of Intestinal Physiopathology, Department of Immunology and Cell Biology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Anat Rec (Hoboken). 2023 May;306(5):1054-1061. doi: 10.1002/ar.24996. Epub 2022 Jun 1.
Intestinal cell stemness, proliferation and differentiation are complex processes all occurring in distinct compartments of the crypt that need to be closely regulated to ensure proper epithelial renewal. The involvement of the Hippo pathway in intestinal epithelial proliferation and regeneration after injury via the regulation of its effectors YAP1 and TAZ has been well-documented over the last decade. The implication of YAP1 and TAZ on intestinal epithelial cell differentiation is less clear. Using intestinal cell models in which the expression of YAP1 and TAZ can be modulated, our group showed that YAP1 inhibits differentiation of the two main intestinal epithelial cell types, goblet and absorptive cells through a specific mechanism involving the repression of prodifferentiation transcription factor CDX2 expression. Further analysis provided evidence that the repressive effect of YAP1 on intestinal differentiation is mediated by regulation of the Hippo pathway by Src family kinase activity. Interestingly, the TAZ paralog does not seem to be involved in this process, which provides another example of the lack of perfect complementarity of the two main Hippo effectors.
肠道细胞的干性、增殖和分化是复杂的过程,均发生在肠隐窝的不同区域,需要密切调控以确保上皮细胞的正常更新。在过去十年中,已有充分文献证明Hippo信号通路通过调节其效应因子YAP1和TAZ参与肠道上皮损伤后的增殖和再生。YAP1和TAZ对肠道上皮细胞分化的影响尚不清楚。利用可调节YAP1和TAZ表达的肠道细胞模型,我们团队发现YAP1通过一种特定机制抑制两种主要肠道上皮细胞类型(杯状细胞和吸收细胞)的分化,该机制涉及抑制促分化转录因子CDX2的表达。进一步分析表明,YAP1对肠道分化的抑制作用是由Src家族激酶活性对Hippo信号通路的调节介导的。有趣的是,TAZ的旁系同源物似乎不参与这一过程,这为两种主要的Hippo效应因子缺乏完美互补性提供了另一个例子。