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1,25-Dihydroxyvitamin D3 preserves intestinal epithelial barrier function from TNF-alpha induced injury via suppression of NF-kB p65 mediated MLCK-P-MLC signaling pathway

机译:1,25-二羟基维生素D3通过抑制NF-κBp65介导的MLCK-P-MLC信号通路来保护肠道上皮屏障功能免受TNF-α诱导的损伤

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摘要

Substantial studies have demonstrated the protective effect of 1,25-Dihydroxyvitamin D3 (1,25(OH)2D3) on intestinal barrier function, but the mechanisms are not fully illustrated. In this study, the effect of 1,25(OH)2D3 on TNF-alpha induced barrier dysfunction was further investigated in Caco-2 cell monolayers. The barrier function of Caco-2 monolayers was evaluated by measuring trans-epithelial electrical resistance (TEER) and FITC-Dextran 40,000 Da (FD-40) trans-membrane flux. ZO-1 and Occludin were chosen as markers of the localization of tight junction (TJ) proteins for immunofluorescence. The expression of MLCK and phosphorylation level of myosin light chain (MLC) were measured by immunoblotting. The activation of NF-kB p65 was analyzed by EMSA and immunofluorescence. The results suggest that 1,25(OH)2D3 preserves intestinal epithelial barrier function from TNF-a. induced injury via suppression of NF-kB p65 mediated activation of MLCK-P-MLC signaling pathway. (C) 2015 Elsevier Inc. All rights reserved.
机译:大量研究表明1,25-二羟基维生素D3(1,25(OH)2D3)对肠屏障功能具有保护作用,但其机理尚未完全阐明。在这项研究中,在Caco-2细胞单层中进一步研究了1,25(OH)2D3对TNF-α诱导的屏障功能障碍的影响。通过测量跨上皮电阻(TEER)和FITC-Dextran 40,000 Da(FD-40)跨膜通量来评估Caco-2单层的屏障功能。选择ZO-1和Occludin作为用于免疫荧光的紧密连接(TJ)蛋白定位的标记。通过免疫印迹测定MLCK的表达和肌球蛋白轻链(MLC)的磷酸化水平。通过EMSA和免疫荧光分析NF-kB p65的活化。结果表明1,25(OH)2D3保留了TNF-a的肠上皮屏障功能。通过抑制NF-κBp65介导的MLCK-P-MLC信号通路的激活而引起的损伤。 (C)2015 Elsevier Inc.保留所有权利。

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