Apical polarity and actomyosin dynamics control Kibra subcellular localization and function in Drosophila Hippo signaling

被引:3
|
作者
Tokamov, Sherzod A. [1 ,2 ]
Nouri, Nicki [1 ]
Rich, Ashley [1 ,3 ]
Buiter, Stephan [1 ]
Glotzer, Michael [1 ]
Fehon, Richard G. [1 ,2 ]
机构
[1] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Dev Regenerat & Stem Cell Biol, Chicago, IL 60637 USA
[3] Duke Univ, Dept Cell Biol, Sch Med, Durham, NC USA
基金
美国国家卫生研究院;
关键词
REGULATE CELL-PROLIFERATION; WING IMAGINAL DISC; TUMOR-SUPPRESSOR; EPITHELIAL-CELLS; PAR PROTEINS; F-ACTIN; GROWTH; PATHWAY; SIZE; PHOSPHORYLATION;
D O I
10.1016/j.devcel.2023.08.029
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Hippo pathway is an evolutionarily conserved regulator of tissue growth that integrates inputs from both polarity and actomyosin networks. An upstream activator of the Hippo pathway, Kibra, localizes at the junc-tional and medial regions of the apical cortex in epithelial cells, and medial accumulation promotes Kibra activity. Here, we demonstrate that cortical Kibra distribution is controlled by a tug-of-war between apical polarity and actomyosin dynamics. We show that while the apical polarity network, in part via atypical protein kinase C (aPKC), tethers Kibra at the junctional cortex to silence its activity, medial actomyosin flows promote Kibra-mediated Hippo complex formation at the medial cortex, thereby activating the Hippo pathway. This study provides a mechanistic understanding of the relationship between the Hippo pathway, polarity, and actomyosin cytoskeleton, and it offers novel insights into how fundamental features of epithelial tissue architecture can serve as inputs into signaling cascades that control tissue growth, patterning, and morphogenesis.
引用
收藏
页码:1864 / +
页数:21
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