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Title: Transient receptor potential V4 channel stimulation induces reversible epithelial cell permeability in MDCK cell monolayers. Author: Mukaiyama M, Yamasaki Y, Usui T, Nagumo Y. Journal: FEBS Lett; 2019 Aug; 593(16):2250-2260. PubMed ID: 31206656. Abstract: The transient receptor potential V4 channel (TRPV4) is responsive to a variety of physical and chemical stimuli, including a synthetic agonist GSK1016790A (GSK). Here, we show that TRPV4 is functionally expressed in, and that GSK induces the reversible opening of tight junctions (TJs) in epithelial Madin-Darby canine kidney II monolayers. Stimulation of TRPV4 by GSK induces an increase in fluorescein isothiocyanate-conjugated dextran (4 kDa) permeability and a reduction in transepithelial resistance, and these responses are blocked by pretreatment with the specific TRPV4 antagonist. Small conductance, but not large conductance Ca2+ -activated K+ channels, TRPA1 channel, and cofilin activation are involved in TRPV4-mediated reversible opening of TJs. These results suggest that a novel mechanism underlies TRPV4-mediated regulation of the tightness of epithelial barriers.[Abstract] [Full Text] [Related] [New Search]