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

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 peritoneal macrophage function....

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Veröffentlicht in:Fertility and sterility 1999-09, Vol.72 (3), p.533-538
Hauptverfasser: Loh, Foo-Hoe, Bongso, Ariff, Fong, Chui-Yee, Koh, Dow-Rhoon, Lee, Szu-Hee, Zhao, Hui-Qin
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container_end_page 538
container_issue 3
container_start_page 533
container_title Fertility and sterility
container_volume 72
creator Loh, Foo-Hoe
Bongso, Ariff
Fong, Chui-Yee
Koh, Dow-Rhoon
Lee, Szu-Hee
Zhao, Hui-Qin
description 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 peritoneal 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 3H-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.
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Design: Controlled study of peritoneal 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 3H-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.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/S0015-0282(99)00292-7</identifier><identifier>PMID: 10519630</identifier><identifier>CODEN: FESTAS</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adult ; Ascitic Fluid - pathology ; Ascitic Fluid - physiopathology ; Biological and medical sciences ; Cell cycle, cell proliferation ; Cell Division ; Cell physiology ; coculture ; Coculture Techniques ; endometrial proliferation ; endometriosis ; Endometriosis - pathology ; Endometrium - pathology ; Epithelial Cells - pathology ; Female ; Fundamental and applied biological sciences. 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Design: Controlled study of peritoneal 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 3H-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). 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subjects Adult
Ascitic Fluid - pathology
Ascitic Fluid - physiopathology
Biological and medical sciences
Cell cycle, cell proliferation
Cell Division
Cell physiology
coculture
Coculture Techniques
endometrial proliferation
endometriosis
Endometriosis - pathology
Endometrium - pathology
Epithelial Cells - pathology
Female
Fundamental and applied biological sciences. Psychology
Humans
Macrophages, Peritoneal - physiology
Molecular and cellular biology
Peritoneal macrophages
Stromal Cells - pathology
title Effects of peritoneal macrophages from women with endometriosis on endometrial cellular proliferation in an in vitro coculture model
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