| Literature DB >> 34538217 |
Takashi Kojima1, Yuma Shindo1,2, Takumi Konno1, Yuki Kodera1,3, Wataru Arai1,2, Maki Miyakawa1,4, Kizuku Ohwada1,5, Hiroki Tanaka4, Mitsuhiro Tsujiwaki6, Yuji Sakuma7, Shin Kikuchi8, Tsuyoshi Ohkuni5, Kenichi Takano5, Atsushi Watanabe2, Takayuki Kohno1.
Abstract
Airway and intestinal epithelial permeability barriers are crucial in epithelial homeostasis. High mobility group box 1 (HMGB1), increased by various stimuli, is involved in the induction of airway inflammation, as well as the pathogenesis of inflammatory bowel disease. HMGB1 enhances epithelial hyperpermeability. Two-and-a-half dimensional (2.5D) culture assays are experimentally convenient and induce cells to form a more physiological tissue architecture than 2D culture assays for molecular transfer mechanism analysis. In 2.5D culture, treatment with HMGB1 induced permeability of FITC-dextran into the lumen formed by human lung, nasal and intestinal epithelial cells. The tricellular tight junction molecule angulin-1/LSR is responsible for the epithelial permeability barrier at tricellular contacts and contributes to various human airway and intestinal inflammatory diseases. In this review, we indicate the mechanisms including angulin-1/LSR and multiple signaling in dysfunction of the epithelial permeability barrier induced by HMGB1 in 2.5D culture of human airway and intestinal epithelial cells.Entities:
Keywords: 2.5d matrigel cultures; EW-7197; PF431396; PYK2; TGF-β; angulin-1/LSR; cell metabolism; claudins; epithelial permeability barriers; hmgb1; human intestinal epithelial cell line CACO-2; normal human nasal epithelial cells; normal human pulmonary epithelial cells; p63; proinflammatory cytokines; tight junctions; tnfα-antibody; tricellulin
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Year: 2021 PMID: 34538217 PMCID: PMC9067465 DOI: 10.1080/21688370.2021.1972760
Source DB: PubMed Journal: Tissue Barriers ISSN: 2168-8362