The Canonical Notch Signaling Was Involved in the Regulation of Intestinal Epithelial Cells Apoptosis after Intestinal Ischemia/Reperfusion Injury

被引:21
作者
Chen, Guoqing [1 ]
Zhang, Zhicao [1 ]
Cheng, Yingdong [1 ]
Xiao, Weidong [1 ]
Qiu, Yuan [1 ]
Yu, Min [1 ]
Sun, Lihua [1 ]
Wang, Wensheng [1 ]
Du, Guangsheng [1 ]
Gu, Yingchao [1 ]
Peng, Ke [1 ]
Xu, Chao [1 ]
Yang, Hua [1 ]
机构
[1] Third Mil Med Univ, Xinqiao Hosp, Dept Gen Surg, Chongqing 400037, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; notch signaling; intestine; ischemia/reperfusion; ISCHEMIA-REPERFUSION INJURY; DOWN-REGULATION; GENES; ACTIVATION; INDUCTION; PROTECTS; PROLIFERATION; PRETREATMENT; INHIBITION; EXPRESSION;
D O I
10.3390/ijms15057883
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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 gamma-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.
引用
收藏
页码:7883 / 7896
页数:14
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