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Tsc1 regulates tight junction independent of mTORC1.

Mingqiang LaiWenchong ZouZe-Long HanLing ZhouZeyou QiuJuan ChenSheng ZhangPinglin LaiKai LiYue ZhangLi LiangYu JiangZhipeng ZouXiao-Chun Bai
Published in: Proceedings of the National Academy of Sciences of the United States of America (2021)
Tuberous sclerosis complex 1 (Tsc1) is a tumor suppressor that functions together with Tsc2 to negatively regulate the mechanistic target of rapamycin complex 1 (mTORC1) activity. Here, we show that Tsc1 has a critical role in the tight junction (TJ) formation of epithelium, independent of its role in Tsc2 and mTORC1 regulation. When an epithelial cell establishes contact with neighboring cells, Tsc1, but not Tsc2, migrates from the cytoplasm to junctional membranes, in which it binds myosin 6 to anchor the perijunctional actin cytoskeleton to β-catenin and ZO-1. In its absence, perijunctional actin cytoskeleton fails to form. In mice, intestine-specific or inducible, whole-body Tsc1 ablation disrupts adherens junction/TJ structures in intestine or skin epithelia, respectively, causing Crohn's disease-like symptoms in the intestine or psoriasis-like phenotypes on the skin. In patients with Crohn's disease or psoriasis, junctional Tsc1 levels in epithelial tissues are markedly reduced, concomitant with the TJ structure impairment, suggesting that Tsc1 deficiency may underlie TJ-related diseases. These findings establish an essential role of Tsc1 in the formation of cell junctions and underpin its association with TJ-related human diseases.
Keyphrases
  • blood brain barrier
  • gene expression
  • stem cells
  • endothelial cells
  • high resolution
  • depressive symptoms
  • adipose tissue
  • cell cycle arrest
  • cell therapy
  • single molecule