Increased expression of antimicrobial peptides and lysozyme in colonic epithelial cells of patients with ulcerative colitis

被引:174
作者
Fahlgren, A
Hammarström, S
Danielsson, Å
Hammarström, ML [1 ]
机构
[1] Umea Univ, Dept Immunol, S-90185 Umea, Sweden
[2] Umea Univ, Dept Med, Gastroenterol Sect, S-90185 Umea, Sweden
关键词
alpha-defensin; beta-defensin; inflammatory bowel disease; intestinal epithelial cell; lysozyme;
D O I
10.1046/j.1365-2249.2003.02035.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The impact of chronic inflammation on the expression of human alpha -defensins 5 and 6 (HD-5, HD-6), beta -defensins 1 and 2 (hBD-1, hBD-2) and lysozyme in epithelial cells of small and large intestine was investigated. Intestinal specimens from 16 patients with ulcerative colitis (UC), 14 patients with Crohn's disease (CD) and 40 controls with no history of inflammatory bowel disease were studied. mRNA expression levels of the five defence molecules were determined in freshly isolated epithelial cells by real-time quantitative RT-PCR. Specific copy standards were used allowing comparison between the expression levels of the different defensins. HD-5 and lysozyme protein expression was also studied by immunohistochemistry. Colonic epithelial cells from patients with UC displayed a significant increase of hBD-2, HD-5, HD-6 and lysozyme mRNA as compared to epithelial cells in controls. Lysozyme mRNA was expressed at very high average copy numbers followed by HD-5, HD-6, hBD-1 and hBD-2 mRNA. HD-5 and lysozyme protein was demonstrated in metaplastic Paneth-like cells in UC colon. There was no correlation between hBD-2 mRNA levels and HD-5 or HD-6 mRNA levels in colon epithelial cells of UC patients. Colonic epithelial cells of Crohn's colitis patients showed increased mRNA levels of HD-5 and lysozyme mRNA whereas ileal epithelial cells of Crohn's patients with ileo-caecal inflammation did not. Chronic inflammation in colon results in induction of hBD-2 and alpha-defensins and increased lysozyme expression. hBD-1 expression levels in colon remain unchanged in colitis. The high antimicrobial activity of epithelial cells in chronic colitis may be a consequence of changes in the epithelial lining, permitting adherence of both pathogenic bacteria and commensals directly to the epithelial cell surface.
引用
收藏
页码:90 / 101
页数:12
相关论文
共 48 条
[31]   Cryptdin-3 induces novel apical conductance(s) in Cl- secretory, including cystic fibrosis, epithelia [J].
Merlin, D ;
Yue, G ;
Lencer, WI ;
Selsted, ME ;
Madara, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (02) :C296-C302
[32]   Nuclear factor-κB activation and innate immune response in microbial pathogen infection [J].
Naumann, M .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (08) :1109-1114
[33]   Regulation of human β-defensins by gastric epithelial cells in response to infection with Helicobacter pylori or stimulation with interleukin-1 [J].
O'Neil, DA ;
Cole, SP ;
Martin-Porter, E ;
Housley, MP ;
Liu, L ;
Ganz, T ;
Kagnoff, MF .
INFECTION AND IMMUNITY, 2000, 68 (09) :5412-5415
[34]  
O'Neil DA, 1999, J IMMUNOL, V163, P6718
[35]   Localization of human intestinal defensin 5 in Paneth cell granules [J].
Porter, EM ;
Liu, L ;
Oren, A ;
Anton, PA ;
Ganz, T .
INFECTION AND IMMUNITY, 1997, 65 (06) :2389-2395
[36]  
Quayle AJ, 1998, AM J PATHOL, V152, P1247
[37]   Unifying hypothesis for inflammatory bowel disease and associated colon cancer: Sticking the pieces together with sugar [J].
Rhodes, JM .
LANCET, 1996, 347 (8993) :40-44
[38]   Epithelial antimicrobial peptides:: innate local host response elements [J].
Schröder, JM .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 56 (1-2) :32-46
[39]   The intestinal mucus layer from patients with inflammatory bowel disease harbors high numbers of bacteria compared with controls [J].
Schultsz, C ;
van den Berg, FM ;
ten Kate, FW ;
Tytgat, GNJ ;
Dankert, J .
GASTROENTEROLOGY, 1999, 117 (05) :1089-1097
[40]   Biological insights into TCRγδ+ and TCRαβ+ intraepithelial lymphocytes provided by serial analysis of gene expression (SAGE) [J].
Shires, J ;
Theodoridis, E ;
Hayday, AC .
IMMUNITY, 2001, 15 (03) :419-434