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DOI 10.1016/j.ejogrb.2005.03.017

Медицинская библиотека · European journal of obstetrics, gynecology, and reproductive biology · 2005

Effect of activin A on tumor necrosis factor-alpha/intercellular adhesion molecule-1 pathway in endometrial stromal cells.

Mangioni Silvia, Viganò Paola, Florio Pasquale, Borghi Orietta, Vignali Michele, Petraglia Felice, Di Blasio Anna Maria

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Аннотация

UNLABELLED: OBJECTIVE[S]: Activin A and inhibin A are growth factors expressed by human endometrium involved in the control of endometrial functions. In the present study we investigated the effects of activin A and inhibin A in modulating the tumor necrosis factor (TNF)-alpha/intercellular adhesion molecule (ICAM)-1 system in cultured human endometrial stromal cells.

STUDY

DESIGN

Endometrial samples were obtained from 34 reproductive age women undergoing laparoscopy for benign ovarian cysts or infertility. Endometrial stromal cells were cultured and soluble ICAM-1 and TNF-alpha were measured in cell-free supernatants following treatment with or without activin A or inhibin A. Cell surface ICAM-1 was assayed by flow cytometry by staining endometrial cells with specific monoclonal antibodies.

RESULTS

Activin A and inhibin A did not influence either the expression of cell surface ICAM-1 or soluble ICAM-1 shedding by cultured endometrial cells. On the other hand, TNF-alpha secretion significantly increased in presence of activin A but not of inhibin A.

CONCLUSIONS

Since TNF-alpha modulates several endometrial processes such as menstruation, proliferation, apoptosis, implantation and decidualization, an effect of activin A in the physiological control of endometrium is further supported by the present data.

Для цитирования: Mangioni Silvia, Viganò Paola, Florio Pasquale, Borghi Orietta, Vignali Michele, Petraglia Felice, Di Blasio Anna Maria. Effect of activin A on tumor necrosis factor-alpha/intercellular adhesion molecule-1 pathway in endometrial stromal cells.. European journal of obstetrics, gynecology, and reproductive biology. 2005. DOI: 10.1016/j.ejogrb.2005.03.017.

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