Regulation of epithelial syndecan-1 expression by inflammatory cytokines

被引:44
作者
Day, RM
Mitchell, TJ
Knight, SC
Forbes, A
机构
[1] St Marks Hosp, IBD Res Grp, Harrow HA1 3UJ, Middx, England
[2] Univ London Imperial Coll Sci Technol & Med, Div Biomed Sci, Leukocyte Biol Sect, London SW7 2BP, England
[3] Univ London Imperial Coll Sci Technol & Med, Div Invest Sci, Antigen Presentat Res Grp, Harrow HA1 3UJ, Middx, England
关键词
colitis-ulcerative; Crohn; cytokine; epithelium; syndecan-1;
D O I
10.1016/S1043-4666(03)00091-7
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
Syndecan-1 is expressed on the basolateral surface of columnar epithelium and contributes to wound repair by facilitating increased growth factor binding. Inflammatory bowel disease (11313) is associated with reduced syndecan-1 expression in areas of inflamed mucosa that is likely to impair mucosal healing. Reduced syndecan-1 expression in 11313 may be related to the presence of increased inflammatory cytokines. To test this hypothesis, monolayers of HT29 and T84 colonic epithelial cells were stimulated with tumour necrosis factor (TNF)-alpha, interleukin (IL)-1beta or IL-6. Stimulation of HT29 cells with TNF-alpha and IL-1beta resulted in reversible down-regulation of syndecan-1 at both protein and mRNA levels but little effect was observed with IL-6. Loss of syndecan-1 expression was caused by shedding of the ectodomain as revealed by increased levels of soluble syndecan-1 measured in the conditioned medium of stimulated cells. No increase in cytoplasmic staining accompanied the loss of cell surface syndecan-1 expression. TNF-alpha and IL-1beta are capable of down-regulating syndecan-1 expression and may account in part for the reduced expression of syndecan-1 seen in IBD. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:224 / 233
页数:10
相关论文
共 27 条
[1]   BIOLOGY OF THE SYNDECANS - A FAMILY OF TRANSMEMBRANE HEPARAN-SULFATE PROTEOGLYCANS [J].
BERNFIELD, M ;
KOKENYESI, R ;
KATO, M ;
HINKES, MT ;
SPRING, J ;
GALLO, RL ;
LOSE, EJ .
ANNUAL REVIEW OF CELL BIOLOGY, 1992, 8 :365-393
[2]  
BLOOM S, 1995, CLIN EXP IMMUNOL, V101, P157
[3]  
Carey DJ, 1997, BIOCHEM J, V327, P1
[4]   Expression of syndecan-1 in inflammatory bowel disease and a possible mechanism of heparin therapy [J].
Day, R ;
Ilyas, M ;
Talbot, I ;
Forbes, A ;
Daszak, P .
DIGESTIVE DISEASES AND SCIENCES, 1999, 44 (12) :2508-2515
[5]   Quantitative PCR analysis of TNF-alpha and IL-1 beta mRNA levels in pediatric IBD mucosal biopsies [J].
Dionne, S ;
Hiscott, J ;
DAgata, I ;
Duhaime, A ;
Seidman, EG .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (07) :1557-1566
[6]   INDUCED EXPRESSION OF SYNDECAN IN HEALING WOUNDS [J].
ELENIUS, K ;
VAINIO, S ;
LAATO, M ;
SALMIVIRTA, M ;
THESLEFF, I ;
JALKANEN, M .
JOURNAL OF CELL BIOLOGY, 1991, 114 (03) :585-595
[7]   Shedding of syndecan-1 and-4 ectodomains is regulated by multiple signaling pathways and mediated by a TIMP-3-sensitive metalloproteinase [J].
Fitzgerald, ML ;
Wang, ZH ;
Park, PW ;
Murphy, G ;
Bernfield, M .
JOURNAL OF CELL BIOLOGY, 2000, 148 (04) :811-824
[8]   IMMUNOCYTOCHEMISTRY OF CELL-SURFACE HEPARAN-SULFATE PROTEOGLYCAN IN MOUSE-TISSUES - A LIGHT AND ELECTRON-MICROSCOPIC STUDY [J].
HAYASHI, K ;
HAYASHI, M ;
JALKANEN, M ;
FIRESTONE, JH ;
TRELSTAD, RL ;
BERNFIELD, M .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1987, 35 (10) :1079-1088
[9]   CELL-SURFACE PROTEOGLYCAN OF MOUSE MAMMARY EPITHELIAL-CELLS IS SHED BY CLEAVAGE OF ITS MATRIX-BINDING ECTODOMAIN FROM ITS MEMBRANE-ASSOCIATED DOMAIN [J].
JALKANEN, M ;
RAPRAEGER, A ;
SAUNDERS, S ;
BERNFIELD, M .
JOURNAL OF CELL BIOLOGY, 1987, 105 (06) :3087-3096
[10]   Suppression of syndecan-1 expression tumor necrosis factor-alpha [J].
Kainulainen, V ;
Nelimarkka, L ;
Jarvelainen, H ;
Laato, M ;
Jalkanen, M ;
Elenius, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) :18759-18766