Vinculin is critical for the robustness of the epithelial cell sheet paracellular barrier for ions

Author:

Konishi Satoshi12,Yano Tomoki1,Tanaka Hiroo134,Mizuno Tomoaki1,Kanoh Hatsuho15,Tsukita Kazuto16,Namba Toshinori7ORCID,Tamura Atsushi134,Yonemura Shigenobu89,Gotoh Shimpei210,Matsumoto Hisako2,Hirai Toyohiro2,Tsukita Sachiko14ORCID

Affiliation:

1. Laboratory of Biological Science, Graduate School of Frontier Biosciences and Graduate School of Medicine, Osaka University, Osaka, Japan

2. Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan

3. Department of Pharmacology, Teikyo University, Tokyo, Japan

4. Strategic Innovation and Research Center, Teikyo University, Tokyo, Japan

5. Graduate School of Biostudies, Kyoto University, Kyoto, Japan

6. Department of Neurology, Graduate School of Medicine, Kyoto University, Kyoto, Japan

7. Graduate School of Arts and Sciences, Tokyo University, Tokyo, Japan

8. Department of Cell Biology, Tokushima University Graduate School of Medical Science, Tokushima, Japan

9. Laboratory for Ultrastructural Research, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan

10. Department of Drug Discovery for Lung Diseases, Graduate School of Medicine, Kyoto University, Kyoto, Japan

Abstract

The paracellular barrier function of tight junctions (TJs) in epithelial cell sheets is robustly maintained against mechanical fluctuations, by molecular mechanisms that are poorly understood. Vinculin is an adaptor of a mechanosensory complex at the adherens junction. Here, we generated vinculin KO Eph4 epithelial cells and analyzed their confluent cell-sheet properties. We found that vinculin is dispensable for the basic TJ structural integrity and the paracellular barrier function for larger solutes. However, vinculin is indispensable for the paracellular barrier function for ions. In addition, TJs stochastically showed dynamically distorted patterns in vinculin KO cell sheets. These KO phenotypes were rescued by transfecting full-length vinculin and by relaxing the actomyosin tension with blebbistatin, a myosin II ATPase activity inhibitor. Our findings indicate that vinculin resists mechanical fluctuations to maintain the TJ paracellular barrier function for ions in epithelial cell sheets.

Funder

Japan Society for the Promotion of Science

Takeda Science Foundation and Uehara Memorial Foundation

Japan Science and Technology Agency

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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