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Am J Reprod Immunol. 2012 Dec;68(6):491-8. doi: 10.1111/aji.12003. Epub 2012 Aug 31.

The localization and regulation of proprotein convertase subtilisin/kexin (PCSK) 6 in human ovary.

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  • 1Department of Obstetrics and Gynecology, University of Tokyo, Tokyo 113-8655, Japan.

Abstract

PROBLEM:

The aim of this study is to evaluate the expression and regulation of proprotein convertase subtilisin/kexin (PCSK) 6, which is known to be an important factor in the production of bone morphogenetic protein (BMP) cytokines in human ovary.

METHOD OF STUDY:

The localization of PCSK 6 protein in normal human ovaries was examined by immunohistochemistry. Human granulosa cells (GC), obtained from 34 patients undergoing ovarian stimulation for in vitro fertilization, were cultured with BMP-2, BMP-6, BMP-7, BMP-15, growth differentiation factor (GDF)-9, and activin-A with or without FSH. PCSK 6 mRNA expression level was evaluated by quantitative real-time reverse transcription and polymerase chain reaction (RT-PCR).

RESULTS:

An immunohistochemistry study revealed that GC expressed PCSK 6 throughout follicular development, beginning in the primary follicle stage, while oocytes expressed PCSK 6 from the primordial follicle stage onwards. An in vitro study demonstrated that BMP-2, BMP-6, BMP-7, and BMP-15, not activin-A and GDF-9, decreased PCSK 6 gene expression in human GC. FSH induced PCSK 6 mRNA in the presence of activin-A or GDF-9. GDF-3, which is an inhibitor of BMP cytokines, also induced PCSK 6 mRNA expression.

CONCLUSIONS:

PCSK 6, which is a critical factor to produce BMP cytokines, was suppressed with BMP stimulation in human GC, suggesting the presence of a negative feedback system in the follicular development process.

© 2012 John Wiley & Sons A/S.

PMID:
22935039
[PubMed - indexed for MEDLINE]
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