Distinct Polarity Cues Direct Taz/Yap and TGFβ Receptor Localization to Differentially Control TGFβ-Induced Smad Signaling

被引:63
作者
Narimatsu, Masahiro [1 ]
Samavarchi-Tehrani, Payman [1 ]
Varelas, Xaralabos [2 ]
Wrana, Jeffrey L. [1 ,3 ]
机构
[1] Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON 1X5 ON, Canada
[2] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
[3] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
关键词
HIPPO PATHWAY; STEM-CELLS; TAZ; YAP; GROWTH; ACTIVATION;
D O I
10.1016/j.devcel.2015.02.019
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We and others have shown that the Hippo pathway effectors TAZ and YAP direct Smad activity to regulate TGF beta family-induced cellular responses in stem cell and cancer biology. In polarized epithelial cells we showed that the Crumbs complex promotes Hippo-dependent cytoplasmic TAZ/YAP localization that restricts TGF beta-induced Smad nuclear accumulation and activity. In this Developmental Cell issue, basal-lateral restriction of TGF beta receptors is proposed as the sole mechanism suppressing Smad signaling in epithelial cells. Here we show that basal recruitment of TGF beta receptors occurs subsequent to Hippo-dependent suppression of Smad activity by cytoplasmic TAZ/YAP. Our results demonstrate that receptor sequestration and Hippo control of activated Smads are distinct events regulating TGF beta signaling in polarized epithelia and raise interesting questions about the function of these pathways in controlling Smad signaling in development, homeostasis, and disease. This Matters Arising Response addresses the Nallet-Staub et al. (2015) Matters Arising, published concurrently in Developmental Cell.
引用
收藏
页码:652 / 656
页数:5
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