Milk Fat Globule-EGF Factor 8 Is a Critical Protein for Healing of Dextran Sodium Sulfate-Induced Acute Colitis in Mice

被引:33
作者
Chogle, Ashish [1 ,2 ]
Bu, Heng-Fu [2 ]
Wang, Xiao [2 ]
Brown, Jeffrey B. [1 ,2 ]
Chou, Pauline M. [3 ]
Tan, Xiao-Di [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Dept Pediat, Feinberg Sch Med, Div Gastroenterol & Hepatol, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Childrens Mem Res Ctr, Ctr Intestinal & Liver Inflammat Res, Chicago, IL 60611 USA
[3] Northwestern Univ, Dept Pathol, Feinberg Sch Med, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
TNBS-INDUCED COLITIS; ACID-INDUCED COLITIS; GENE-EXPRESSION; INFLAMMATION; MELATONIN; GHRELIN; RATS; HORMONE; PEPTIDE; DISEASE;
D O I
10.2119/molmed.2010.00074
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
Milk fat globule-EGF factor 8 (MFG-E8) has been shown to play an important role in maintaining the integrity of the intestinal mucosa and to accelerate healing of the mucosa in septic mice. Herein, we (a) analyzed the expression of MFG-E8 in the gut of wildtype (WI) C57BL/6 (MFG-E8) mice with and without dextran sulfate sodium (DSS)-induced colitis, (b) characterized the pathological changes in intestinal mucosa of MFG-E8(+/+) and MFG-E8(-/-) mice with DSS-induced colitis and (c) examined the therapeutic role of MFG-E8 in inflammatory bowel disease by using DSS-induced colitis model. Our data documented that there was an increase in colonic and rectal MFG-E8 expression in MFG-E8(+/+) mice during the development of DSS colitis. MFG-E8 levels in both tissues decreased to below baseline during the recovery phase in mice with colitis. Changes in MFG-E8 gene expression correlated to the levels of inflammatory response and crypt-epithelial injury in both colonic and rectal mucosa in MFG-E8(+/+) mice. MFG-E8(-/-) mice developed more severe crypt-epithelial injury than MFG-E8(+/+) mice during exposure to DSS with delayed healing of intestinal epithelium during the recovery phase of DSS colitis. Administration of MFG-E8 during the recovery phase ameliorated colitis and promoted mucosal repair in both MFG-E8(-/-) and MFG-E8(+/+) mice, indicating that lack of MFG-E8 causes increased susceptibility to colitis and delayed mucosal healing. These data suggest that MGF-E8 is an essential protective factor for gut epithelial homeostasis, and exogenous administration of MFG-E8 may represent a novel therapeutic target in inflammatory bowel disease. (C) 2011 The Feinstein Institute for Medical Research, www.feinsteininstitute.org Online address: htfp://www.molmed.org doi: 10.2119/molmed.2010.00074
引用
收藏
页码:502 / 507
页数:6
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