Effect of sulfated GAGs on the expression and activation of MMP-2 and MMP-9 in corneal and dermal explant cultures

被引:43
作者
Isnard, N [1 ]
Robert, L [1 ]
Renard, G [1 ]
机构
[1] Hop Hotel Dieu, Lab Rech Ophtalmol, F-75004 Paris, France
关键词
GAGs; MMP-s; keratocytes; cornea; fibroblasts; skin;
D O I
10.1016/S1065-6995(03)00167-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been shown previously that hyaluronan (HA) added to fibroblast and keratocyte cell cultures or corneal explant cultures produces an up-regulation of MMP-2 and MMP-9 expression and activation. Here, we examine the effect of sulfated GAG-s, chondroitin 4 and 6 sulfate (CS4, CS6), dermatan sulfate (DS), keratan sulfate (KS) and heparan sulfate (HS) on MMP-2 and 9 expression and activation under the same culture conditions. It appears that CS4 has only minor effects, KS inhibits MMP-2 activation and CS6, DS and HS increase MMP-2 activation in corneal explant cultures. For skin explant cultures, DS, KS and HS strongly increase MMP-9 activation, whereas KS inhibits and DS increases MMP-2 activation. All these effects can be strongly inhibited by the addition of an antibody to CD44, except CS6 and DS. Activation by these two GAGs was only slightly affected, supporting the contention that the effects of HA, CS4, KS and HS are mediated by one of the isoforms of this CD44 receptor. The physio-pathological significance of these results is discussed for cornea and skin ageing, because of the divergent evolution with in vitro ageing of the relative proportions of GAGs synthesised by these two cell types. (C) 2003 Published by Elsevier Ltd.
引用
收藏
页码:779 / 784
页数:6
相关论文
共 28 条
[1]  
ASHTON N, 1960, TRANSPARENCY CORNEA, P17
[2]  
Azar DT, 1996, CORNEA, V15, P18
[3]  
BROWN CT, 1995, J CELL BIOCHEM, V59, P57, DOI 10.1002/jcb.240590108
[4]  
Ellerbroek SM, 1999, BIOESSAYS, V21, P940, DOI 10.1002/(SICI)1521-1878(199911)21:11<940::AID-BIES6>3.3.CO
[5]  
2-A
[6]  
FINI ME, 1992, ACTA OPHTHALMOL, V70, P26
[7]   Keratan sulfate: structure, biosynthesis, and function [J].
Funderburgh, JL .
GLYCOBIOLOGY, 2000, 10 (10) :951-958
[8]   Influence of heparin(s) on the interleukin-1-β-induced expression of collagenase, stromelysin-1, and tissue inhibitor of metalloproteinase-1 in human gingival fibroblasts [J].
Gogly, B ;
Hornebeck, W ;
Groult, N ;
Godeau, G ;
Pellat, B .
BIOCHEMICAL PHARMACOLOGY, 1998, 56 (11) :1447-1454
[9]   Effect of heparin on the production of matrix metalloproteinases and tissue inhibitors of metalloproteinases by human dermal fibroblasts [J].
Gogly, B ;
Dridi, M ;
Hornebeck, W ;
Bonnefoix, M ;
Godeau, G ;
Pellat, B .
CELL BIOLOGY INTERNATIONAL, 1999, 23 (03) :203-209
[10]   CHARACTERIZATION OF THE MOLECULAR MECHANISM INVOLVED IN THE ACTIVATION OF HYALURONAN SYNTHETASE BY PLATELET-DERIVED GROWTH-FACTOR IN HUMAN MESOTHELIAL CELLS [J].
HELDIN, P ;
ASPLUND, T ;
YTTERBERG, D ;
THELIN, S ;
LAURENT, TC .
BIOCHEMICAL JOURNAL, 1992, 283 :165-170