首页|动力蛋白相关蛋白1抑制剂对肠黏膜上皮细胞缺血再灌注损伤的干预作用及其机制

动力蛋白相关蛋白1抑制剂对肠黏膜上皮细胞缺血再灌注损伤的干预作用及其机制

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目的 探讨动力蛋白相关蛋白1(Drp1)抑制剂对肠黏膜上皮细胞缺血再灌注损伤的干预作用并分析其机制。方法 将人大肠黏膜上皮细胞系Caco-2分为对照组、模型组、Drp1抑制剂组,对照组正常培养细胞,模型组、Drp1抑制剂组均采用缺氧12 h后复氧2 h的方法构建缺氧复氧模型,Drp1抑制剂组在H/R前给予Drp1抑制剂Mdivi-1干预。采用CCK-8法检测细胞活力,线粒体超氧化物指示剂检测线粒体活性氧(ROS)含量,JC-1法检测线粒体膜电位,流式细胞术检测细胞凋亡率,Western blotting法检测细胞Drp1、线粒体融合蛋白2(Mfn2)蛋白。结果 细胞活力对照组>Drp1抑制剂组>模型组(P均<0。05);细胞内线粒体ROS含量模型组>Drp1抑制剂组>对照组,线粒体膜电位对照组>Drp1抑制剂组>模型组(P均<0。05);细胞凋亡率模型组>Drp1抑制剂组>对照组(P均<0。05);细胞Drp1蛋白表达模型组>Drp1抑制剂组>对照组,Mfn2蛋白表达对照组>Drp1抑制剂组>模型组(P均<0。05)。结论 Drp1抑制剂可减轻肠黏膜上皮细胞缺血再灌注损伤,其机制可能与改善线粒体功能障碍、减少细胞凋亡有关。
Intervention effect of Drp1 inhibitor on ischemia-reperfusion injury in intestinal mucosal epithelial cells
Objective To observe the intervention effect of dynamin-related protein 1(Drp1)inhibitor on ischemia-reperfusion injury of intestinal mucosal epithelial cells and to analyze its mechanism.Methods Human colorectal muco-sal epithelial cells Caco-2 were divided into the control group,model group,and Drp1 inhibitor group,respectively.The cells in the control group were cultured normally.In the model group and Drp1 inhibitor group,hypoxia-reperfusion mod-els were constructed by using the method of hypoxia for 12 h followed by reoxygenation for 2 h;cells in the Drp1 inhibitor group were given the intervention of the Drp1 inhibitor-Mdivi-1 before the H/R treatment.Cell viability was detected by CCK-8 assay,mitochondrial reactive oxygen species(ROS)content was detected by mitochondrial superoxide indicator,mitochondrial membrane potential level was detected by JC-1 assay,apoptosis rate was detected by flow cytometry,and the expression levels of Drp1,and mitochondrial fusion protein 2(mitofusin2,Mfn2)were detected by Western blotting.Results Cell viability was as follows:control group>Drp1 inhibitor group>model group(all P<0.05),intracellular mitochondrial ROS content was as follows:model group>Drp1 inhibitor group>control group,mitochondrial membrane potential was as follows:control group>Drp1 inhibitor group>model group(all P<0.05),apoptosis rate was as follows:model group>Drp1 inhibitor group>control group(all P<0.05),cellular Drp1 protein expression was as follows:model group>Drp1 inhibitor group>control group,and Mfn2 protein expression was as follows:control group>Drp1 inhibitor group>model group(all P<0.05).Conclusion Drp1 inhibitor could reduce ischemia-reperfusion injury in intestinal mucosal epithelial cells,and its mechanism might be related to improving mitochondrial dysfunction and reducing apopto-sis.

dynamin-related protein 1intestinal ischemia-reperfusion injurymitofusion 2mitochondrial func-tionmitochondrial dynamics

图拉妮萨·喀迪尔、张贻帼、景祎馨、廖师师、罗杰、丁可、陈榕、孟庆涛

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武汉大学人民医院麻醉科,武汉 430060

动力蛋白相关蛋白1 肠缺血再灌注损伤 线粒体融合蛋白2 线粒体功能 线粒体动力学

国家自然科学基金资助项目中央高校基本科研业务费专项资金项目湖北省重点实验室开放项目

821721552042022kf10822021KEY032

2024

山东医药
山东卫生报刊社

山东医药

CSTPCD
影响因子:1.225
ISSN:1002-266X
年,卷(期):2024.64(5)
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