A baboon model for endometriosis: implications for fertility

被引:74
作者
Hastings, Julie M. [1 ]
Fazleabas, Asgerally T. [1 ]
机构
[1] Univ Illinois, Dept Obstet & Gynecol MC808, Coll Med, Chicago, IL 60612 USA
关键词
D O I
10.1186/1477-7827-4-S1-S7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endometriosis is one of the most common causes of chronic pelvic pain and infertility in women in the reproductive age group. Although the existence of this disease has been known for over 100 years our current knowledge of its pathogenesis and the pathophysiology of its related infertility remains unclear. Several reasons contribute to our lack of knowledge, the most critical being the difficulty in carrying out objective long-term studies in women. Thus, we and others have developed a model of this disease in the non-human primate, the baboon (Papio anubis). Intraperitoneal inoculation of autologous menstrual endometrium results in the development of endometriotic lesions with gross morphological characteristics similar to those seen in the human. Multiple factors have been implicated in endometriosis-associated infertility. We have described aberrant levels of factors involved in multiple pathways important in the establishment of pregnancy, in the endometrium of baboons induced with endometriosis. Specifically, we have observed dysregulation of proteins involved in invasion, angiogenesis, methylation, cell growth, immunomodulation, and steroid hormone action. These data suggest that, in an induced model of endometriosis in the baboon, an increased angiogenic capacity, decreased apoptotic potential, progesterone resistance, estrogen hyper-responsiveness, and an inability to respond appropriately to embryonic signals contribute to the reduced fecundity associated with this disease.
引用
收藏
页数:14
相关论文
共 140 条
[1]   Cyr61, a deregulated gene in endometriosis [J].
Absenger, Y ;
Hess-Stumpp, H ;
Kreft, B ;
Krätzschmar, J ;
Haendler, B ;
Schütze, N ;
Regidor, PA ;
Winterhager, E .
MOLECULAR HUMAN REPRODUCTION, 2004, 10 (06) :399-407
[2]   CLINICAL AND EXPERIMENTAL ENDOMETRIOSIS [J].
ALLEN, E ;
PETERSON, LF ;
CAMPBELL, ZB .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1954, 68 (01) :356-375
[3]   Altered expression if interleukin-18 in the peritoneal fluid of women with endometriosis [J].
Arici, A ;
Matalliotakis, I ;
Goumenou, A ;
Koumantakis, G ;
Vassiliadis, S ;
Mahutte, NG .
FERTILITY AND STERILITY, 2003, 80 (04) :889-894
[4]   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
[5]  
AYERS JWT, 1987, FERTIL STERIL, V47, P925
[6]   Role of DNA 5-methylcytosine transferase in cell transformation by fos [J].
Bakin, AV ;
Curran, T .
SCIENCE, 1999, 283 (5400) :387-390
[7]   Angiogenic activity and IL-8 concentrations in peritoneal fluid and sera in endometriosis [J].
Barcza, E ;
Rózewska, ES ;
Kaminski, P ;
Demkow, U ;
Bobrowska, K ;
Marianowski, L .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2002, 79 (03) :229-235
[8]   Efficacy of anti-tumor necrosis factor therapy in the treatment of spontaneous endometriosis in baboons [J].
Barrier, BF ;
Bates, GW ;
Leland, MM ;
Leach, DA ;
Robinson, RD ;
Propst, AM .
FERTILITY AND STERILITY, 2004, 81 :775-779
[9]   Short synthetic endostatin peptides inhibit endothelial migration in vitro and endometriosis in a mouse model [J].
Becker, CM ;
Sampson, DA ;
Short, SM ;
Javaherian, K ;
Folkman, J ;
D'Amato, RJ .
FERTILITY AND STERILITY, 2006, 85 (01) :71-77
[10]   Endostatin inhibits the growth of endometriotic lesions but does not affect fertility [J].
Becker, CM ;
Sampson, DA ;
Rupnick, MA ;
Rohan, RM ;
Efstathiou, JA ;
Short, SM ;
Taylor, GA ;
Folkman, J ;
D'Amato, RJ .
FERTILITY AND STERILITY, 2005, 84 :1144-1155