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Division of Reproductive Endocrinology and Fertility, Division of Gynecologic Oncology (S.H.), Departments of Obstetrics and Gynecology and Pharmacology (J.E.), University of North Carolina School of Medicine Chapel Hill, North Carolina 27514
Address all correspondence and requests for reprints to: Jouko Halme, M.D., Ph.D., Department of Obstetrics and Gynecology, University of California School of Medicine, Los Angeles, California 90024-1740.
We studied the in vitro secretion of macrophagederived growth factor (MDGF) activity by peritoneal macrophages from fertile and infertile women. Peritoneal fluid was obtained from 55 women undergoing laparoscopy for evaluation and treatment of infertility or for tubal sterilization. Isolated macrophages were plated in tissue culture wells and incubated in Dulbecco's Modified Eagle's Medium plus 0.2% lactalbumin hydrolyzate at 37 C for 24 h. Medium MDGF activity was assayed by determining the ability of medium to stimulate [3H] thymidine incorporation in BALB-c 3T3 fibroblasts. Macrophages from 23 women released significant MDGF activity in vitro; the release was linear for up to 72 h. Among the 55 women, macrophages from 10 of 36 (28%) women with normal pelvic anatomy or tubal occlusion/pelvic adhesions released significant MDGF activity. In contrast, macrophages from 13 of 19 (68%) women with endometriosis, a significantly higher proportion (P < 0.02), released MDGF. The finding that endometriosis is associated with in vivo primed peritoneal macrophages that produce MDGF in vitro may help to explain the proliferation or maintenance of endometrial tissue in the peritoneal cavity.
* This work was supported by USPHS Grant HD-21546 (to J.H.) and in part by Grant CA-30479 (to J.E.).
Received October 1, 1987.
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