Rack1 regulates cellular patterning and polarity in the mouse cochlea

被引:1
|
作者
Yu, Dehong [1 ,2 ,6 ,7 ,8 ]
Deng, Di [5 ]
Chen, Binjun [3 ,4 ]
Sun, Haojie [3 ,4 ]
Lyu, Jihan [3 ,4 ]
Zhao, Yu [5 ]
Chen, Ping [6 ,7 ]
Wu, Hao [1 ,2 ]
Ren, Dongdong [3 ,4 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Otolaryngol Head & Neck Surg, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Ear Inst, Sch Med, Shanghai, Peoples R China
[3] Fudan Univ, Eye & ENT Hosp, ENT Inst, Dept Otorhinolaryngol, Shanghai, Peoples R China
[4] Fudan Univ, NHC Key Lab Hearing Med, Shanghai 200031, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Otorhinolaryngol Head & Neck Surg, Chengdu, Peoples R China
[6] Emory Univ, Dept Cell Biol, Atlanta, GA 30322 USA
[7] Emory Univ, Dept Otolaryngol, Atlanta, GA USA
[8] Shanghai Univ, Sch Life Sci, Materdicine Lab, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
PROTEIN RACK1; E-CADHERIN; LOCALIZATION; ADHESION; EXPRESSION; VANGL2; LINK;
D O I
10.1016/j.yexcr.2022.113387
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rack1 features seven WD40 repeats that fold into a multifaceted scaffold used to build signaling complexes in a context-dependent manner. Previous in vitro studies have revealed associations between Rack1 and many other proteins. Rack 1 is required for establishing planar cell polarity (PCP) in zebrafish and Xenopus. However, any molecular role of Rack1 in protein complexes or polarity regulation remains unclear. Here, we show that Rack1 is an essential gene in mice. Conditional knockout of Rack1 shortened the cochlear duct and induced cellular patterning defects characteristic of defective convergent extension (this PCP process is mediated by cellular junctional remodeling in the developing cochlear epithelium). Also, cochlear hair cells were no longer uniformly oriented in Rack1 conditional knockout mutants. Rack1 was enriched in the cellular cortices of sensory hair cells. In Rack1-deficient cochleae, E-cadherin expression at the cellular boundaries was greatly reduced. Together, the findings reveal a molecular role of Rack1 in PCP signaling that likely involves modulation of E-cadherin levels at the adherens junctions of the plasma membrane.
引用
收藏
页数:6
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