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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >HO-1/CO Maintains Intestinal Barrier Integrity through NF- κ B/MLCK Pathway in Intestinal HO-1 -/- Mice
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HO-1/CO Maintains Intestinal Barrier Integrity through NF- κ B/MLCK Pathway in Intestinal HO-1 -/- Mice

机译:HO-1 / CO通过肠道HO-1 / - 小鼠的NF-κB/ mlck途径保持肠道阻隔完整性

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摘要

Background . Intestinal barrier injury is an important contributor to many diseases. We previously found that heme oxygenase-1 (HO-1) and carbon monoxide (CO) protect the intestinal barrier. This study is aimed at elucidating the molecular mechanisms of HO-1/CO in barrier loss. Materials and Methods . We induced gut leakiness by injecting carbon tetrachloride (CCl 4 ) to wildtype or intestinal HO-1-deficient mice. In addition, we administrated tumor necrosis factor- α (TNF- α ) to cells with gain- or loss-of-HO-1 function. The effects of HO-1/CO maintaining intestinal barrier integrity were investigated in vivo and in vitro . Results . Cobalt protoporphyrin and CO-releasing molecule-2 alleviated colonic mucosal injury and TNF- α levels; upregulated tight junction (TJ) expression; and inhibited epithelial I κ B- α degradation and phosphorylation, NF- κ B p65 phosphorylation, long MLCK expression, and MLC-2 phosphorylation after administration of CCl 4 . Zinc protoporphyrin completely reversed these effects. These findings were further confirmed in vitro , using Caco-2 cells with gain- or loss-of-HO-1-function after TNF- α . Pretreated with JSH-23 (NF- κ B inhibitor) or ML-7 (long MLCK inhibitor), HO-1 overexpression prevented TNF- α -induced TJ disruption, while HO-1 shRNA promoted TJ damage even in the presence of JSH-23 or ML-7, thus suggesting that HO-1 dependently protected intestinal barrier via the NF- κ B p65/MLCK/p-MLC-2 pathway. Intestinal HO-1-deficient mice further demonstrated the effects of HO-1 in maintaining intestinal barrier integrity and its relative mechanisms. Alleviated hepatic fibrogenesis and serum ALT levels finally confirmed the clinical significance of HO-1/CO repairing barrier loss in liver injury. Conclusion . HO-1/CO maintains intestinal barrier integrity through the NF- κ B/MLCK pathway. Therefore, the intestinal HO-1/CO-NF- κ B/MLCK system is a potential therapeutic target for diseases with a leaky gut.
机译:背景 。肠势障碍是许多疾病的重要贡献者。我们以前发现血红素氧酶-1(HO-1)和一氧化碳(CO)保护肠道屏障。本研究旨在阐明HO-1 / CO中的障碍损失的分子机制。材料和方法 。我们通过将四氯化碳(CCl 4)注入野生型或肠HO-1缺陷小鼠来诱导肠道泄漏。此外,我们将肿瘤坏死因子 - α(TNF-α)施放到具有HO-1的增益或丧失功能的细胞。在体内和体外研究HO-1 / CO保持肠道阻隔完整性的影响。结果 。钴原卟啉和共同释放的分子-2缓解结肠粘膜损伤和TNF-α水平;上调紧密交界(TJ)表达;并抑制上皮IκB-α降解和磷酸化,NF-κBP65磷酸化,LONG MLCK表达和施用CCL 4后的MLC-2磷酸化。锌原卟啉完全逆转了这些效果。在TNF-α之后使用具有增益或损失的CaCo-2细胞,在体外进一步证实这些发现。用JSH-23(NF-κB抑制剂)或ML-7(LONG MLCK抑制剂)预处理,HO-1过表达防止了TNF-α-诱导的TJ中断,而HO-1 shRNA即使在JSH的存在下也促进了TJ损伤23或ML-7,因此表明HO-1通过NF-κBP65 / MLCK / P-MLC-2途径依赖性保护的肠道屏障。肠道HO-1缺陷小鼠进一步证明了HO-1在保持肠道阻挡完整性及其相对机制方面的影响。缓解肝纤维发生和血清ALT水平最终证实了HO-1 / CO修复肝损伤屏障损失的临床意义。结论 。 HO-1 / CO通过NF-κB/ MLCK途径保持肠道阻挡完整性。因此,肠HO-1 / CO-NF-κB/ MLCK系统是漏气肠道的疾病的潜在治疗靶标。

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