Pro-oxidant and proapoptotic effects of cholesterol oxidation products on human colonic epithelial cells: A potential mechanism of inflammatory bowel disease progression

被引:68
作者
Biasi, Fiorella [1 ]
Mascia, Cinzia [1 ]
Astegiano, Marco [2 ]
Chiarpotto, Elena [1 ]
Nano, Mario [1 ]
Vizio, Barbara [3 ]
Leonarduzzi, Gabriella [1 ]
Poli, Giuseppe [1 ]
机构
[1] Univ Turin, Dept Clin & Biol Sci, San Luigi Gonzaga Hosp, I-10043 Turin, Italy
[2] San Giovanni Battista Hosp, Div Gastroenterol, I-10126 Turin, Italy
[3] Univ Turin, Dept Clin Physiopathol, San Giovanni Battista Hosp, I-10126 Turin, Italy
关键词
Oxysterols; Colonic mucosa; NADPH oxidase; Reactive oxygen species; Apoptosis; Inflammatory bowel disease; Free radicals; OXYSTEROL MIXTURES; ENDOTHELIAL-CELLS; APOPTOSIS; CACO-2; DIETARY; 7-BETA-HYDROXYCHOLESTEROL; 7-KETOCHOLESTEROL; CYTOTOXICITY; INVOLVEMENT; ACTIVATION;
D O I
10.1016/j.freeradbiomed.2009.09.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
With the aim of investigating whether cholesterol oxidation products could contribute to the pathogenesis of the intestinal epithelial barrier dysfunction that occurs in human inflammatory bowel disease (IBD), differentiated versus undifferentiated CaCo-2 cells, an accepted model for human intestinal epithelial cells, were challenged with a dietary-representative mixture of oxysterols. Only differentiated colonic cells were susceptible to the proapoptotic action of the oxysterol mixture, checked both by enzymatic and by morphological methods, mainly because of a very low AI(T phosphorylation pathway compared to the undifferentiated counterparts. Enhanced production of reactive oxygen species by a colonic NADPH oxidase hyperactivation seemed to represent the key event in oxysterol-induced up-regulation of the mitochondrial pathway of programmed death of differentiated CaCo-2 cells. These in vitro findings point to the pro-oxidant and cytotoxic potential of cholesterol oxidation products, of both dietary and endogenous origin, as an important mechanism of induction and/or worsening of the functional impairment of enteric mucosa that characterizes IBD. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1731 / 1741
页数:11
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