TISSUE INHIBITOR OF METALLOPROTEINASES-1 IS DECREASES AND ACTIVATED GELATINASES ARE INCREASED IN CHRONIC WOUNDS

被引:190
作者
BULLEN, EC
LONGAKER, MT
UPDIKE, DL
BENTON, R
LADIN, D
HOU, ZZ
HOWARD, EW
机构
[1] UNIV OKLAHOMA,HLTH SCI CTR,DEPT PATHOL,OKLAHOMA CITY,OK 73190
[2] NYU,MED CTR,INST RECONSTRUCT PLAST SURG,NEW YORK,NY
[3] HENRY FORD HOSP,DIV PLAST & RECONSTRUCT SURG,DETROIT,MI 48202
关键词
TYPE IV COLLAGENASE; TIMP; HEALING; EXTRACELLULAR MATRIX;
D O I
10.1111/1523-1747.ep12612786
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The balance between matrix deposition and tissue turnover is fundamental in wound healing. It is likely that the balance between proteolytic enzymes and their inhibitors contributes to this balance. Matrix metalloproteinases are clearly important in tissue turnover, but their roles in wound healing are poorly understood. To investigate this, fluid from healing wounds resulting from mastectomies was collected from 1 h to 10 d post-surgery, and was analyzed for tissue inhibitor of metalloproteinases-1 concentrations. In all cases, tissue inhibitor of metalloproteinases-1 levels were initially comparable to those in serum, but increased rapidly to significantly higher levels within two days, with a tenfold average increase for five patients. On the other hand, zymography revealed that gelatinase A (72 kDa) levels increased moderately, whereas gelatinase B levels (92 kDa) decreased an average of twofold within 4 d. In contrast, fluid from chronic wounds had significantly more gelatinolytic activity, including lower-molecular-weight proteinase species that may represent activated or superactivated gelatinase fragments, as suggested by immunoprecipitation with specific antibodies. Tissue inhibitor of metalloproteinases-1 levels were lower in chronic than in healing wounds. These data may indicate that excess proteolysis in chronic wounds retards successful healing, and results from an imbalance of proteinase and inhibitors, as well as the presence of higher levels of activated metalloproteinases.
引用
收藏
页码:236 / 240
页数:5
相关论文
共 32 条
[21]   THE C-TERMINAL DOMAIN OF 72-KDA GELATINASE-A IS NOT REQUIRED FOR CATALYSIS, BUT IS ESSENTIAL FOR MEMBRANE ACTIVATION AND MODULATES INTERACTIONS WITH TISSUE INHIBITORS OF METALLOPROTEINASES [J].
MURPHY, G ;
WILLENBROCK, F ;
WARD, RV ;
COCKETT, MI ;
EATON, D ;
DOCHERTY, AJP .
BIOCHEMICAL JOURNAL, 1992, 283 :637-641
[22]   DEMONSTRATION OF 72-KDA AND 92-KDA FORMS OF TYPE-IV COLLAGENASE IN HUMAN SKIN - VARIABLE EXPRESSION IN VARIOUS BLISTERING DISEASES, INDUCTION DURING REEPITHILIALIZATION, AND DECREASE BY TOPICAL GLUCOCORTICOIDS [J].
OIKARINEN, A ;
KYLMANIEMI, M ;
AUTIOHARMAINEN, H ;
AUTIO, P ;
SALO, T .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 101 (02) :205-210
[23]  
PATERSON CA, 1994, INVEST OPHTH VIS SCI, V35, P677
[24]   DISTINCT LOCALIZATION OF COLLAGENASE AND TISSUE INHIBITOR OF METALLOPROTEINASES EXPRESSION IN WOUND-HEALING ASSOCIATED WITH ULCERATIVE PYOGENIC GRANULOMA [J].
SAARIALHOKERE, UK ;
CHANG, ES ;
WELGUS, HG ;
PARKS, WC .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05) :1952-1957
[25]  
SALO T, 1994, LAB INVEST, V70, P176
[26]   TYPE-IV COLLAGENASE(S) AND TIMPS MODULATE ENDOTHELIAL-CELL MORPHOGENESIS IN-VITRO [J].
SCHNAPER, HW ;
GRANT, DS ;
STETLERSTEVENSON, WG ;
FRIDMAN, R ;
DORAZI, G ;
MURPHY, AN ;
BIRD, RE ;
HOYTHYA, M ;
FUERST, TR ;
FRENCH, DL ;
QUIGLEY, JP ;
KLEINMAN, HK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1993, 156 (02) :235-246
[27]  
STETLERSTEVENSO.WG, 1989, J BIOL CHEM, V264, P17374
[28]  
STRICKLIN GP, 1993, AM J PATHOL, V143, P1657
[29]  
WENTWORTH JS, 1992, INVEST OPHTH VIS SCI, V33, P2174
[30]  
WILHELM SM, 1989, J BIOL CHEM, V264, P17213