Literature DB >> 12759153

Endometrial expression and secretion of activin A, but not follistatin, increase in the secretory phase of the menstrual cycle.

Pasquale Florio1, Filiberto M Severi, Stefano Luisi, Pasquapina Ciarmela, Giulia Calonaci, Luigi Cobellis, Felice Petraglia.   

Abstract

OBJECTIVE: Activin A is a growth factor expressed by human endometrium, and its biologic effects are counteracted by follistatin. We evaluate whether activin A and follistatin mRNA and peptide expression as well as protein secretion from human endometrium change throughout the menstrual cycle.
METHODS: In 25 healthy fertile patients, uterine washing fluid was retrieved by hydrosonography. In a subgroup (n = 13), endometrial tissue samples were collected by hysteroscopy during the proliferative (n = 6) or secretory (n = 7) phase of the menstrual cycle. Activin and follistatin mRNA and peptide expression were evaluated by reverse transcriptase-polymerase chain reaction (RT-PCR) and by immunohistochemistry (IHC), respectively. Activin A and follistatin levels were assayed in uterine washing fluids by specific enzyme-linked immunosorbent assays and evaluated according to the endometrial thickness and menstrual cycle days.
RESULTS: Both activin A and follistatin mRNAs were expressed by human endometrium, and their peptides immunolocalized both in proliferative and secretory endometrial epithelial and stromal cells. A significant increase in immunoreactive activin betaA but not in follistatin was observed in glandular epithelium during the secretory phase. Activin A but not follistatin was significantly (P <.0001) higher in the washing fluids collected during the secretory than proliferative phase of the menstrual cycle. In addition, a significant correlation was found between activin A, but not follistatin, and menstrual cycle days (P <.0001) or endometrial thickness (P <.0001).
CONCLUSIONS: Both activin A and follistatin mRNAs are expressed by human endometrium; however, activin A but not follistatin peptide expression and secretion were increased in the secretory phase of the menstrual cycle, suggesting an important role in human endometrium.

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Year:  2003        PMID: 12759153     DOI: 10.1016/s1071-5576(03)00045-5

Source DB:  PubMed          Journal:  J Soc Gynecol Investig        ISSN: 1071-5576


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