Suppression of matrix metalloproteinases inhibits establishment of ectopic lesions by human endometrium in nude mice

被引:243
作者
Bruner, KL
Matrisian, LM
Rodgers, WH
Gorstein, F
Osteen, KG
机构
[1] VANDERBILT UNIV,SCH MED,DEPT OBSTET & GYNECOL,NASHVILLE,TN 37232
[2] VANDERBILT UNIV,SCH MED,DEPT PATHOL,NASHVILLE,TN 37232
[3] VANDERBILT UNIV,SCH MED,DEPT CELL BIOL,NASHVILLE,TN 37232
[4] UNIV ALABAMA,DEPT PATHOL,BIRMINGHAM,AL 35233
[5] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT PATHOL,PHILADELPHIA,PA 19107
关键词
matrilysin; stromelysin; endometriosis; progesterone; TIMP-1;
D O I
10.1172/JCI119478
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
0Matrix metalloproteinases of the stromelysin family are expressed in the human endometrium as a consequence of cellular events during the menstrual cycle that require extracellular matrix remodelling. We have recently documented the presence of these enzymes in lesions of endometriosis, a benign disease that presents as persistent ectopic sites of endometrial tissue, usually within the peritoneal cavity. Endometriosis can develop after retrograde menstruation of endometrial tissue fragments, and establishment of ectopic sites within the peritoneal cavity requires breakdown of extracellular matrix. To examine whether matrix metalloproteinases might contribute to the steroid-dependent epidemiology and cellular pathophysiology of endometriosis, we have developed an experimental model of endometriosis using athymic nude mice as recipients of human endometrial tissue. Our results demonstrate that estrogen treatment of human endometrial tissue in organ culture maintains secretion of matrix metalloproteinases, and promotes establishment of ectopic peritoneal lesions when injected into recipient animals. In contrast, suppressing metalloproteinase secretion in vitro with progesterone treatment, or blocking enzyme activity with a natural inhibitor of metalloproteinases, inhibits the formation of ectopic lesions in this experimental model.
引用
收藏
页码:2851 / 2857
页数:7
相关论文
共 30 条
[1]  
AOKI D, 1994, OBSTET GYNECOL, V83, P220
[2]  
BERGQVIST A, 1988, AM J PATHOL, V121, P337
[3]   TRANSFORMING GROWTH-FACTOR-BETA MEDIATES THE PROGESTERONE SUPPRESSION OF AN EPITHELIAL METALLOPROTEINASE BY ADJACENT STROMA IN THE HUMAN ENDOMETRIUM [J].
BRUNER, KL ;
RODGERS, WH ;
GOLD, LI ;
KORC, M ;
HARGROVE, JT ;
MATRISIAN, LM ;
OSTEEN, KG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7362-7366
[4]  
BUSIEK DF, 1992, J BIOL CHEM, V267, P9087
[5]   PRIMARY STRUCTURE AND CDNA CLONING OF HUMAN FIBROBLAST COLLAGENASE INHIBITOR [J].
CARMICHAEL, DF ;
SOMMER, A ;
THOMPSON, RC ;
ANDERSON, DC ;
SMITH, CG ;
WELGUS, HG ;
STRICKLIN, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2407-2411
[6]   SYSTEMIC ADMINISTRATION OF TIMP IN THE TREATMENT OF COLLAGEN-INDUCED ARTHRITIS IN MICE [J].
CARMICHAEL, DF ;
STRICKLIN, GP ;
STUART, JM .
AGENTS AND ACTIONS, 1989, 27 (3-4) :378-379
[7]  
HALME J, 1995, REPROD MED SURG, P695
[8]   PERITONEAL ENDOMETRIOSIS - ENDOMETRIAL TISSUE IMPLANTATION AS ITS PRIMARY ETIOLOGIC MECHANISM [J].
ISHIMARU, T ;
MASUZAKI, H .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1991, 165 (01) :210-214
[9]   PATHOPHYSIOLOGY OF MILD ENDOMETRIOSIS - REVIEW OF LITERATURE [J].
MAHMOOD, TA ;
TEMPLETON, A .
HUMAN REPRODUCTION, 1990, 5 (07) :765-784
[10]  
MARBAIX E, 1994, J BIOCHEM-TOKYO, V305, P1027