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Tsc1 regulates tight junction independent of mTORC1
Author(s) -
Mingqiang Lai,
Wenchong Zou,
Zelong Han,
Ling Zhou,
Zeyou Qiu,
Juan Chen,
Sheng Zhang,
Pinglin Lai,
Kai Li,
Yue Zhang,
Li Liang,
Yu Jiang,
Zhipeng Zou,
Xiaochun Bai
Publication year - 2021
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2020891118
Subject(s) - tsc1 , adherens junction , microbiology and biotechnology , mtorc1 , biology , actin cytoskeleton , actin , tsc2 , cytoskeleton , cadherin , cell , signal transduction , genetics , pi3k/akt/mtor pathway
Significance The epithelium barrier is vital for sealing body surface and alimentary spaces, preventing paracellular material diffusion and pathogen invasion. We describe here that tuberous sclerosis complex 1 (Tsc1) controls tight junction (TJ) formation to create and maintain the epithelial barrier, independent of its conventional role in mTOR regulation. We found that Tsc1 loss is associated with TJ destruction in patients with TJ-related human diseases, such as inflammatory bowel disease and psoriasis, a common skin disorder. Tsc1 knockout in epithelial cells drives TJ dysfunction, causing Crohn’s disease–like and psoriasis-like signs and symptoms in mice. This function of Tsc1 has significant implications to understand how epithelial cells form TJ to protect us from these diseases.

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