Effects of peritoneal macrophages from women with endometriosis on endometrial cellular proliferation in an in vitro coculture model

被引:23
作者
Loh, FH
Bongso, A
Fong, CY
Koh, DR
Lee, SH
Zhao, HQ
机构
[1] Natl Univ Singapore, Dept Physiol, Singapore 117548, Singapore
[2] Natl Univ Singapore, Dept Pathol, Singapore 117548, Singapore
基金
英国医学研究理事会;
关键词
peritoneal macrophages; endometriosis; endometrial proliferation; coculture;
D O I
10.1016/S0015-0282(99)00292-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To study the effects of peritoneal macrophages on endometrial cellular proliferation in an in vitro coculture model and to compare the magnitude of these effects between macrophages from women with endometriosis and normal women. Design: Controlled study of peritorneal macrophage function. Setting: University hospital. Patient(s): Patients with a normal peritoneal cavity (n = 15) and with pelvic endometriosis (n = 20) undergoing laparoscopy. Intervention(s): Peritoneal macrophages were cocultured with endometrial epithelial and stromal cells; endometrial cell cultures without macrophage coculture acted as controls. Main Outcome Measure(s): Endometrial cellular proliferation measured by H-3-thymidine incorporation. Result(s): Endometrial epithelial cells cocultured with peritoneal macrophages from women with endometriosis showed significantly increased proliferation compared with cocultures using macrophages from normal women when assessed at 24 hours (1.56 versus 1.03 times, respectively, over control) and at 72 hours (1.55 versus 1.10 times over control). Endometrial stromal cells cocultured with peritoneal macrophages from women with endometriosis similarly exhibited increased proliferation compared with cocultures using macrophages from normal women when assessed at 24 hours (1.65 versus 1.17 times over control) and at 72 hours (1.65 versus 1.21 times over control). Conclusion(s): Peritoneal macrophages of patients with endometriosis stimulate cellular proliferation of endometrial epithelial and stromal cells in vitro. (Fertil Steril(R) 1999;72:533-8. (C) 1999 by American Society for Reproductive Medicine.).
引用
收藏
页码:533 / 538
页数:6
相关论文
共 28 条
[1]  
*AM FERT SOC, 1985, FERTIL STERIL, V43, P351
[2]  
BRAUN DP, 1994, FERTIL STERIL, V61, P78
[3]   Cytolysis of eutopic and ectopic endometrial cells by peripheral blood monocytes and peritoneal macrophages in women with endometriosis [J].
Braun, DP ;
Gebel, H ;
Rana, N ;
Dmowski, WP .
FERTILITY AND STERILITY, 1998, 69 (06) :1103-1108
[4]   Inhibition of transforming growth factor-beta 1 alters the growth, anchor-dependent cell aggregation and integrin mRNA expression in human promonocytes: implications for endometriosis and peritoneal adhesion formation [J].
Dou, QC ;
Williams, RS ;
Chegini, N .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (05) :383-391
[5]   INVASIVENESS OF ENDOMETRIOTIC CELLS IN-VITRO [J].
GAETJE, R ;
KOTZIAN, S ;
HERRMANN, G ;
BAUMANN, R ;
STARZINSKIPOWITZ, A .
LANCET, 1995, 346 (8988) :1463-1464
[6]   PERITONEAL-MACROPHAGES FROM PATIENTS WITH ENDOMETRIOSIS RELEASE GROWTH-FACTOR ACTIVITY INVITRO [J].
HALME, J ;
WHITE, C ;
KAUMA, S ;
ESTES, J ;
HASKILL, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 66 (05) :1044-1049
[7]   INCREASED ACTIVATION OF PELVIC MACROPHAGES IN INFERTILE WOMEN WITH MILD ENDOMETRIOSIS [J].
HALME, J ;
BECKER, S ;
HAMMOND, MG ;
RAJ, MHG ;
RAJ, S .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1983, 145 (03) :333-337
[8]  
HALME J, 1984, OBSTET GYNECOL, V64, P151
[9]  
Jurgensen A, 1996, FERTIL STERIL, V66, P369
[10]  
KAUMA S, 1988, OBSTET GYNECOL, V72, P13