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KMID : 1143120200100020020
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Asia Pacific Allergy
2020 Volume.10 No. 2 p.20 ~ p.20
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DsRNA induction of microRNA-155 disrupt tight junction barrier by modulating claudins
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Hiranuma Hisato
Gon Yasuhiro
Maruoka Shuichiro
Kozu Yutaka
Yamada Shiho
Fukuda Asami
Kurosawa Yusuke
Tetsuo Shimizu
Nakagawa Yoshiko
Mizumura Kenji
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Abstract
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Background: The impaired barrier function of the airway epithelium due to RNA virus infection is closely related to the development and exacerbation of allergic airway inflammation.
Objective: In this study, we investigated the roles of microRNAs on the mechanisms of double-stranded RNA (dsRNA)-induced epithelial barrier dysfunction.
Methods: 16HBE14o- human bronchial epithelial cells were grown to confluence on Transwell inserts and exposed to poly-I:C. We studied epithelial barrier function by measuring transepithelial electrical resistance and paracellular flux of fluorescent markers and structure of tight junctions by immunofluorescence microscopy.
Results: Poly-I:C treated 16HBE14o- cells increased paracellular permeability. Knockdown of Toll-like receptor 3 and TRIF abrogated these effects. The expression of microRNA-155 (miR-155) was increased by poly-I:C in dose-dependent manner. Transfection of mir155 mimics into 16HBE14o- cells increased permeability and inhibited tight junction formation. Transfection of miR-155 inhibitor suppressed poly-I:C-induced barrier disruption. Poly-I:C treatment significantly decreased the expression of claudin members?claudin-1, -3, -4, -5, -9, -11, -16, -18 and -19. Transfection of miR-155 mimics showed similar changing expression pattern of claudin members with those of poly-I:C treatment.
Conclusion: These results suggest that RNA virus infection can impair the epithelial barrier disruption mechanism by down-regulation of claudin members through the induction of miR-155.
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KEYWORD
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dsRNA, Airway epithelial cells, Tight junction, Virus, Claudins
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