The Second Clinical College (Guangdong Provincial Hospital of Chinese Medicine), Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
World J Gastroenterol. 2018 Jul 14;24(26):2867-2877. doi: 10.3748/wjg.v24.i26.2867.
To explore the protective effects and underlying mechanisms of total polysaccharides of the Sijunzi decoction (TPSJ) on the epithelial barriers .
Caco-2 cell monolayers were treated with or without TPSJ in the presence or absence of TNF-α, and paracellular permeability and transepithelial electrical resistance (TEER) were measured to evaluate the epithelial barrier function. Immunofluorescence and western blotting were respectively used to evaluate the distribution and expression of the tight junction proteins claudin 1, claudin 2, zo3, and occludin in Caco-2 cells. Western blotting was also used to evaluate the cellular expression of myosin light chain (MLC), phosphorylated MLC (pMLC), MLC kinase (MLCK), and nuclear factor (NF)-κB p65.
TPSJ promoted the proliferation of Caco-2 cells and inhibited TNF-α-induced secretion of pro-inflammatory cytokines. Furthermore, TPSJ significantly ameliorated both the reduction of TEER and the increased paracellular permeability observed in tumor necrosis factor (TNF)-α-damaged Caco-2 monolayers. Furthermore, TPSJ remarkably attenuated TNF-α-induced morphological changes, downregulated the expression of claudin 1, claudin 2, zo3, and occludin, and markedly suppressed TNF-α-mediated upregulation of p-MLC and MLCK expression. Finally, TPSJ inhibited the activation and expression of NF-κB p65.
Our results demonstrate that TPSJ alleviates the TNF-α-induced impairment of the intestinal epithelial cell barrier function by suppressing NF-κB p65-mediated phosphorylation of MLCK and MLC.
探讨四君子汤总多糖(TPSJ)对上皮屏障的保护作用及其机制。
用或不用 TNF-α 处理 Caco-2 细胞单层,测量细胞旁通透性和跨上皮电阻(TEER),以评估上皮屏障功能。免疫荧光和 Western blot 分别用于评估紧密连接蛋白 Claudin 1、Claudin 2、Zo3 和 Occludin 在 Caco-2 细胞中的分布和表达。Western blot 还用于评估肌球蛋白轻链(MLC)、磷酸化 MLC(pMLC)、肌球蛋白轻链激酶(MLCK)和核因子(NF)-κB p65 的细胞表达。
TPSJ 促进 Caco-2 细胞增殖,抑制 TNF-α诱导的促炎细胞因子分泌。此外,TPSJ 显著改善了 TNF-α损伤的 Caco-2 单层中观察到的 TEER 降低和细胞旁通透性增加。此外,TPSJ 显著减弱了 TNF-α诱导的形态变化,下调 Claudin 1、Claudin 2、Zo3 和 Occludin 的表达,并显著抑制了 TNF-α介导的 p-MLC 和 MLCK 表达上调。最后,TPSJ 抑制了 NF-κB p65 的激活和表达。
我们的结果表明,TPSJ 通过抑制 NF-κB p65 介导的 MLCK 和 MLC 的磷酸化来减轻 TNF-α诱导的肠上皮细胞屏障功能障碍。