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

被引:151
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
相关论文
共 70 条
[1]   YAP/TAZ Incorporation in the β-Catenin Destruction Complex Orchestrates the Wnt Response [J].
Azzolin, Luca ;
Panciera, Tito ;
Soligo, Sandra ;
Enzo, Elena ;
Bicciato, Silvio ;
Dupont, Sirio ;
Bresolin, Silvia ;
Frasson, Chiara ;
Basso, Giuseppe ;
Guzzardo, Vincenza ;
Fassina, Ambrogio ;
Cordenonsi, Michelangelo ;
Piccolo, Stefano .
CELL, 2014, 158 (01) :157-170
[2]   Identification of stem cells in small intestine and colon by marker gene Lgr5 [J].
Barker, Nick ;
van Es, Johan H. ;
Kuipers, Jeroen ;
Kujala, Pekka ;
van den Born, Maaike ;
Cozijnsen, Miranda ;
Haegebarth, Andrea ;
Korving, Jeroen ;
Begthel, Harry ;
Peters, Peter J. ;
Clevers, Hans .
NATURE, 2007, 449 (7165) :1003-U1
[3]   Crypt stem cells as the cells-of-origin of intestinal cancer [J].
Barker, Nick ;
Ridgway, Rachel A. ;
van Es, Johan H. ;
van de Wetering, Marc ;
Begthel, Harry ;
van den Born, Maaike ;
Danenberg, Esther ;
Clarke, Alan R. ;
Sansom, Owen J. ;
Clevers, Hans .
NATURE, 2009, 457 (7229) :608-U119
[4]   Restriction of intestinal stem cell expansion and the regenerative response by YAP [J].
Barry, Evan R. ;
Morikawa, Teppei ;
Butler, Brian L. ;
Shrestha, Kriti ;
de la Rosa, Rosemarie ;
Yan, Kelley S. ;
Fuchs, Charles S. ;
Magness, Scott T. ;
Smits, Ron ;
Ogino, Shuji ;
Kuo, Calvin J. ;
Camargo, Fernando D. .
NATURE, 2013, 493 (7430) :106-+
[5]   β-catenin and TCF mediate cell positioning in the intestinal epithelium by controlling the expression of EphB/EphrinB [J].
Batlle, E ;
Henderson, JT ;
Beghtel, H ;
van den Born, MMW ;
Sancho, E ;
Huls, G ;
Meeldijk, J ;
Robertson, J ;
van de Wetering, M ;
Pawson, T ;
Clevers, H .
CELL, 2002, 111 (02) :251-263
[6]   Intestinal label-retaining cells are secretory precursors expressing Lgr5 [J].
Buczacki, Simon J. A. ;
Zecchini, Heather Ireland ;
Nicholson, Anna M. ;
Russell, Roslin ;
Vermeulen, Louis ;
Kemp, Richard ;
Winton, Douglas J. .
NATURE, 2013, 495 (7439) :65-69
[7]   The Hippo signaling pathway restricts the oncogenic potential of an intestinal regeneration program [J].
Cai, Jing ;
Zhang, Nailing ;
Zheng, Yonggang ;
de Wilde, Roeland F. ;
Maitra, Anirban ;
Pan, Duojia .
GENES & DEVELOPMENT, 2010, 24 (21) :2383-2388
[8]   YAP1 increases organ size and expands undifferentiated progenitor cells [J].
Camargo, Fernando D. ;
Gokhale, Sumita ;
Johnnidis, Jonathan B. ;
Fu, Dongdong ;
Bell, George W. ;
Jaenisch, Rudolf ;
Brummelkamp, Thijn R. .
CURRENT BIOLOGY, 2007, 17 (23) :2054-2060
[9]   The Hippo Transducer TAZ Confers Cancer Stem Cell-Related Traits on Breast Cancer Cells [J].
Cordenonsi, Michelangelo ;
Zanconato, Francesca ;
Azzolin, Luca ;
Forcato, Mattia ;
Rosato, Antonio ;
Frasson, Chiara ;
Inui, Masafumi ;
Montagner, Marco ;
Parenti, Anna R. ;
Poletti, Alessandro ;
Daidone, Maria Grazia ;
Dupont, Sirio ;
Basso, Giuseppe ;
Bicciato, Silvio ;
Piccolo, Stefano .
CELL, 2011, 147 (04) :759-772
[10]   Tead2 expression levels control the subcellular distribution of Yap and Taz, zyxin expression and epithelial-mesenchymal transition [J].
Diepenbruck, Maren ;
Waldmeier, Lorenz ;
Ivanek, Robert ;
Berninger, Philipp ;
Arnold, Phil ;
van Nimwegen, Erik ;
Christofori, Gerhard .
JOURNAL OF CELL SCIENCE, 2014, 127 (07) :1523-1536