Activation of Epidermal Growth Factor Receptor Mediates Mucin Production Stimulated by p40, a Lactobacillus rhamnosus GG-derived Protein

被引:112
作者
Wang, Lihong [1 ]
Cao, Hailong [2 ]
Liu, Liping [1 ]
Wang, Bangmao [2 ]
Walker, W. Allan [3 ]
Acra, Sari A. [1 ]
Yan, Fang [1 ]
机构
[1] Vanderbilt Univ, Dept Pediat, Div Gastroenterol Hepatol & Nutr, Med Ctr, Nashville, TN 37232 USA
[2] Tianjin Med Univ, Dept Gastroenterol, Gen Hosp, Tianjin 300052, Peoples R China
[3] Harvard Univ, Mucosal Immunol & Biol Res Ctr, Massachusetts Gen Hosp, Sch Med, Boston, MA 02114 USA
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金; 美国国家卫生研究院;
关键词
INTESTINAL EPITHELIAL-CELLS; GENE-EXPRESSION; IN-VITRO; DEPENDENT MECHANISM; SOLUBLE-PROTEIN; DRUG-DELIVERY; MOUSE STOMACH; MUCUS LAYERS; SECRETION; COLON;
D O I
10.1074/jbc.M114.553800
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
The mucus layer coating the gastrointestinal tract serves as the first line of intestinal defense against infection and injury. Probiotics promote mucin production by goblet cells in the intestine. p40, a Lactobacillus rhamnosus GG-derived soluble protein, has been shown to transactivate the EGF receptor (EGFR) in intestinal epithelial cells, which is required for inhibition of apoptosis and preservation of barrier function in the colon, thereby ameliorating intestinal injury and colitis. Because activation of EGFR has been shown to up-regulate mucin production in goblet cells, the purpose of this study was to investigate the effects and mechanisms of p40 regulation of mucin production. p40 activated EGFR and its downstream target, Akt, in a concentration-dependent manner in LS174T cells. p40 stimulated Muc2 gene expression and mucin production in LS174T cells, which were abolished by inhibition of EGFR kinase activity, down-regulation of EGFR expression by EGFR siRNA transfection, or suppression of Akt activation. Treatment with p40 increased mucin production in the colonic epithelium, thus thickening the mucus layer in the colon of wild type, but not of Egfr(wa5) mice, which have a dominant negative mutation in the EGFR kinase domain. Furthermore, inhibition of mucin-type O-linked glycosylation suppressed the effect of p40 on increasing mucin production and protecting intestinal epithelial cells from TNF-induced apoptosis in colon organ culture. Thus, these results suggest that p40-stimulated activation of EGFR mediates up-regulation of mucin production, which may contribute to the mechanisms by which p40 protects the intestinal epithelium from injury.
引用
收藏
页码:20234 / 20244
页数:11
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