Runt-related transcription factor 2 (RUNX2) inhibits apoptosis of intestinal epithelial cells in Crohn's disease

被引:4
|
作者
Gu, Liugen [1 ]
Zhao, Juan [2 ]
Zhang, Shiqing [2 ]
Xu, Weisong [3 ]
Ni, Runzhou [2 ]
Liu, Xiaojuan [4 ]
机构
[1] Nantong Univ, Affiliated Hosp 2, Dept Gastroenterol, Nantong 226001, Jiangsu, Peoples R China
[2] Nantong Univ, Affiliated Hosp, Dept Gastroenterol, Nantong 226001, Jiangsu, Peoples R China
[3] Secondary Peoples Hosp Nantong, Dept Gastroenterol, Nantong 226001, Jiangsu, Peoples R China
[4] Nantong Univ, Dept Pathogen Biol, Nantong 226001, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Crohn's disease; Intestinal epithelial cells; Apoptosis; Runx2; p53; INFLAMMATORY-BOWEL-DISEASE; COLITIS; P53; RESISTANCE; MICROBIOTA; BARRIER; STRESS; HEALTH; CANCER; MODEL;
D O I
10.1016/j.prp.2017.11.004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Apoptosis in intestinal epithelial cells (IECs) prevents the development of Crohn's disease (CD), a type of inflammatory bowel disease (IBD). Runt-related transcription factor 2 (Runx2) inhibits apoptosis in osteosarcoma-derived U2OS cells via down-regulating the transcriptional activity of p53. However, the expression and function of Runx2 in CD remain unclear. In this study, Runx2 protein levels were decreased in the intestinal epithelial cells (IECs) of CD patients and in a mouse 2, 4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis model; in contrast, the expression levels of p53 and Bax, a p53-target gene, were increased. In a TNF-alpha-treated HT29 cell colitis model, the down-regulation of Runx2 was accompanied by the up-regulation of apoptotic markers, including cleaved caspase-3 and Bax. Furthermore, Runx2 overexpression effectively decreased TNF-alpha-induced Bax and cleaved caspase-3 expression levels. In conclusion, our data indicated that Runx2 might protect IECs from apoptosis in CD, thus revealing a novel molecular target for treating CD.
引用
收藏
页码:245 / 252
页数:8
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