Butyrate enhances major histocompatibility complex class I, HLA-DR and ICAM-1 antigen expression on differentiated human intestinal epithelial cells

被引:23
作者
Siavoshian, S
Blottiere, HM
Bentouimou, N
Cherbut, C
Galmiche, JP
机构
[1] INRA, F-44316 NANTES 03, FRANCE
[2] HOP G&R LAENNEC, CTR RECH NUTR HUMAINE, LAB FONCT DIGEST & NUTR, NANTES, FRANCE
关键词
butyrate; colon; epithelial cells; HLA-DR; short-chain fatty acids;
D O I
10.1046/j.1365-2362.1996.2180561.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Besides its metabolic role, butyrate, a byproduct of colonic fermentation, can modulate colonocyte proliferation and the expression of various molecules. In inflammatory bowel diseases, epithelial cells express HLA class II molecules and may behave as antigen-presenting cells. This study was performed to characterize the effect of butyrate on major histocompatibility complex expression by human colonocytes in comparison with interferon-gamma. Five cell lines displaying different differentiation features were analysed for antigen expression by flow cytofluorimetry. All lines expressed class I antigens, whereas only SW 1116 cells express HLA-DR. On these cells, butyrate and interferon-gamma strongly enhanced HLA-DR and ICAM-1 expression, whereas a mild increase in class I antigens was noted. Moreover, an increase in class I antigens was observed on two other differentiated cell lines, and it was synergistic with interferon-gamma. Butyrate, by its modulation of HLA-DR, ICAM-1 and HLA class I expression, may act on antigen presentation and, thus, influence some inflammatory processes.
引用
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页码:803 / 810
页数:8
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