首页> 外文期刊>International Journal of Molecular Sciences >The Canonical Notch Signaling Was Involved in the Regulation of Intestinal Epithelial Cells Apoptosis after Intestinal Ischemia/Reperfusion Injury
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The Canonical Notch Signaling Was Involved in the Regulation of Intestinal Epithelial Cells Apoptosis after Intestinal Ischemia/Reperfusion Injury

机译:典型的Notch信号参与肠缺血/再灌注损伤后肠上皮细胞凋亡的调节。

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Notch signaling plays a critical role in the maintenance of intestinal homeostasis. The aim of the present study was to investigate the role of Notch signaling in the apoptosis of intestinal epithelial cells after intestinal ischemia reperfusion (I/R) injury. Male C57BL/6 mice were subjected to sham operation or I/R injury. Intestinal tissue samples were collected at 12 h after reperfusion. TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling) staining showed that intestinal I/R injury induced significantly increased apoptosis of intestinal epithelial cells. Meanwhile, the mRNA expression of Jagged1, DLL1, Notch2, and Hes5, and protein expression of NICD2 and Hes5 were increased significantly after I/R injury in intestinal epithelial cells. In an in vitro IEC-6 culture model, flow cytometry analyses showed that inhibition of Notch signaling by γ-secretase inhibitor DAPT and the suppression of Hes5 expression using siRNA both significantly increased the apoptosis of IEC-6 cells under the condition of hypoxia/reoxygenation (H/R). In conclusion, the Notch2/Hes5 signaling pathway was activated and involved in the regulation of intestinal epithelial cells apoptosis in intestinal I/R injury.
机译:Notch信号在维持肠道稳态中起着至关重要的作用。本研究的目的是调查Notch信号在肠缺血再灌注(I / R)损伤后在肠上皮细胞凋亡中的作用。对雄性C57BL / 6小鼠进行假手术或I / R损伤。再灌注后12小时收集肠组织样品。 TUNEL(末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记)染色显示肠I / R损伤诱导肠上皮细胞凋亡显着增加。同时,肠上皮细胞I / R损伤后,Jagged1,DLL1,Notch2和Hes5的mRNA表达以及NICD2和Hes5的蛋白表达显着增加。在体外IEC-6培养模型中,流式细胞仪分析表明,γ-分泌酶抑制剂DAPT对Notch信号的抑制和使用siRNA抑制Hes5表达均在缺氧/复氧条件下显着增加了IEC-6细胞的凋亡。 (水平/垂直)。总之,Notch2 / Hes5信号通路被激活,并参与肠I / R损伤中肠上皮细胞凋亡的调节。

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