Dual role of YAP and TAZ in renewal of the intestinal epithelium

被引:148
作者
Imajo, Masamichi [1 ,2 ,3 ]
Ebisuya, Miki [4 ,5 ]
Nishida, Eisuke [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Biostudies, Dept Cell & Dev Biol, Sakyo Ku, Kyoto 6068502, Japan
[2] JST, CREST, Chiyoda Ku, Tokyo 1020075, Japan
[3] Kyoto Univ, Grad Sch Biostudies, Lab Bioimaging & Cell Signaling, Sakyo Ku, Kyoto 6068501, Japan
[4] Kyoto Univ, Career Path Promot Unit Young Life Scientist, Sakyo Ku, Kyoto 6068501, Japan
[5] RIKEN, Ctr Dev Biol, Lab Reconstitut Dev Biol, Kobe, Hyogo 6500047, Japan
关键词
HIPPO SIGNALING PATHWAY; ORGAN SIZE CONTROL; CELL SELF-RENEWAL; LARGE GENE LISTS; STEM-CELLS; PROMOTES APOPTOSIS; WNT/BETA-CATENIN; TUMOR-SUPPRESSOR; GROWTH-CONTROL; CANCER CELLS;
D O I
10.1038/ncb3084
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The rapidly self-renewing intestinal epithelium represents an exquisite model for stem cell biology. So far, genetic studies in mice have uncovered crucial roles for several signalling pathways in the tissue. Here we show, by using intestine-specific gene transfer (iGT), that Hippo signalling effectors, YAP and TAZ, promote both the proliferation of intestinal stem/progenitor cells and their differentiation into goblet cells. These functions of YAP/TAZ are regulated by the upstream Hippo pathway kinases MST1/2 and LATS1/2. Moreover, we identify TEADs and Klf4 as partner transcription factors of YAP/TAZ in the proliferation and differentiation processes, respectively. These results indicate that Hippo signalling plays a dual role in renewal of the intestinal epithelium through the regulation of two different processes, stem/progenitor cell proliferation and differentiation into goblet cells, using two different types of transcription factor. Moreover, iGT should provide a robust platform to elucidate molecular mechanisms of intestinal epithelium self-renewal.
引用
收藏
页码:7 / +
页数:23
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