Experimental endometriosis - The nude mouse as a xenographic host

被引:56
作者
Bruner-Tran, KL [1 ]
Webster-Clair, D [1 ]
Osteen, KG [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Womens Reprod Hlth Res Ctr, Nashville, TN 37232 USA
来源
ENDOMETRIOSIS: EMERGING RESEARCH AND INTERVENTION STRATEGIES | 2002年 / 955卷
关键词
MMPs; progesterone; nude mouse/mice; cytokine action;
D O I
10.1111/j.1749-6632.2002.tb02793.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Endometriosis is a complex disease that can develop as a consequence of retrograde menstruation, occurring in association with the cyclic loss of endometrial tissue in primates and humans. In addition, progression of disease parallels a woman's exposure to ovarian steroids, rarely occurring prior to menarche and generally resolving following menopause. Because of the cost of developing primate models to study endometriosis, numerous small animal models have been established to approach various elements related to the pathophysiology of this disease. Our laboratory has developed an experimental endometriosis model using nude mice as a xenographic host for human tissues. Our goal is to approach the basic cellular mechanisms of estrogen and progesterone action that link these hormones to the development or prevention of endometriosis. In our initial studies, we have sought to understand steroid-associated regulation of matrix metalloproteinases (MMPs) with regard to the development of experimental endometriosis. Using both short-term organ cultures and nude mice as xenographic hosts of human tissue, we have demonstrated a critical role of progesterone and progesterone-associated cytokines in preventing the initial establishment of experimental disease. Women with endometriosis appear to lack normal endometrial responsiveness to progesterone, resulting in altered expression of several MMPs and an enhanced ability of these tissues to establish ectopic lesions in nude mice. Developing a better understanding of the impairments in the normal endometrial physiology of women with endometriosis should aid in the development of better treatment or diagnostic strategies.
引用
收藏
页码:328 / 342
页数:15
相关论文
共 51 条
[1]   Progesterone receptor isoform A but not B is expressed in endometriosis [J].
Attia, GR ;
Zeitoun, K ;
Edwards, D ;
Johns, A ;
Carr, BR ;
Bulun, SE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (08) :2897-2902
[2]   The SCID mouse: an experimental model for endometriosis [J].
Awwad, JT ;
Sayegh, RA ;
Tao, XJ ;
Hassan, T ;
Awwad, ST ;
Isaacson, K .
HUMAN REPRODUCTION, 1999, 14 (12) :3107-3111
[3]   ESTROGEN AND PROGESTERONE RECEPTORS IN ENDOMETRIOTIC TISSUE AND ENDOMETRIUM - COMPARISON OF DIFFERENT CYCLE PHASES AND AGES [J].
BERGQVIST, A ;
FERNO, M .
HUMAN REPRODUCTION, 1993, 8 (12) :2211-2217
[4]  
BERGQVIST A, 1985, AM J PATHOL, V121, P337
[5]   STUDY OF PLASMA PROGESTERONE, OESTRADIOL-17-BETA, PROLACTIN AND LH LEVELS, AND OF LUTEAL PHASE APPEARANCE OF OVARIES IN PATIENTS WITH ENDOMETRIOSIS AND INFERTILITY [J].
BROSENS, IA ;
KONINCKX, PR ;
CORVELEYN, PA .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1978, 85 (04) :246-250
[6]   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
[7]   Suppression of matrix metalloproteinases inhibits establishment of ectopic lesions by human endometrium in nude mice [J].
Bruner, KL ;
Matrisian, LM ;
Rodgers, WH ;
Gorstein, F ;
Osteen, KG .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2851-2857
[8]   Progesterone and transforming growth factor-β coordinately regulate suppression of endometrial matrix metalloproteinases in a model of experimental endometriosis [J].
Bruner, KL ;
Etsenberg, E ;
Gorstein, F ;
Osteen, KG .
STEROIDS, 1999, 64 (09) :648-653
[9]   The potential role of environmental toxins in the pathophysiology of endometriosis [J].
Bruner-Tran, KL ;
Rier, SE ;
Eisenberg, E ;
Osteen, KG .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 1999, 48 :45-52
[10]   THE MAINE-WOMENS-HEALTH-STUDY .1. OUTCOMES OF HYSTERECTOMY [J].
CARLSON, KJ ;
MILLER, BA ;
FOWLER, FJ .
OBSTETRICS AND GYNECOLOGY, 1994, 83 (04) :556-565