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PLoS One ; 9(6): e99393, 2014.
Article in English | MEDLINE | ID: mdl-24932501

ABSTRACT

Anti-mullerian hormone (AMH) is thought to reflect the growth of follicles and the ovarian function. However, the role of AMH in culture medium during in vitro maturation (IVM) on oocyte quality and subsequent development potential is unclear. The objective of this study is to investigate the effect of recombinant human AMH (rh-AMH) supplemented into IVM medium on oocyte quality. Cumulus-oocyte complexes (COCs) were obtained from ICR mice and cultured in vitro with the different concentrations (0-1,000 ng/ml) of rh-AMH. Following 16-18 h of culture, quantitative PCR and ELISA were performed to analyze GDF9 and BMP15 mRNA expression and protein production from the oocytes. Subsequently, in vitro fertilization (IVF) and early embryonic development were employed to further evaluate the quality of in vitro matured oocytes. The results showed that AMH was only expressed in cumulus cells but not in the oocytes. However, AMH most specific receptor, AMHR-II, was expressed in both oocytes and cumulus cells. The levels of GDF9 and BMP15 expression and blastocyst formation rate were significantly increased (p<0.05) when the IVM medium was supplemented with 100 ng/ml of rh-AMH. With AdH1-SiRNA/AMH for knocking down of AMH expression during IVM significantly reduced (p<0.05) the levels of GDF9 and BMP15 expression and blastocysts formation rate. These results suggest that AHM improves oocytes quality by up-regulating GDF9 and BMP15 expressions during IVM.


Subject(s)
Anti-Mullerian Hormone/pharmacology , Oocytes/drug effects , Animals , Anti-Mullerian Hormone/administration & dosage , Anti-Mullerian Hormone/biosynthesis , Blastocyst/drug effects , Bone Morphogenetic Protein 15/biosynthesis , Bone Morphogenetic Protein 15/genetics , Cells, Cultured , Culture Media/pharmacology , Cumulus Cells/drug effects , Cumulus Cells/metabolism , Dose-Response Relationship, Drug , Embryonic Development , Female , Fertilization in Vitro , Gene Knockdown Techniques , Growth Differentiation Factor 9/biosynthesis , Growth Differentiation Factor 9/genetics , Mice , Mice, Inbred ICR , Oocytes/cytology , Oocytes/metabolism , Polymerase Chain Reaction , RNA, Small Interfering/pharmacology , Receptors, Peptide/biosynthesis , Receptors, Peptide/genetics , Receptors, Transforming Growth Factor beta/biosynthesis , Receptors, Transforming Growth Factor beta/genetics , Recombinant Proteins/pharmacology
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