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Reprod Domest Anim ; 55(7): 833-843, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32335951

ABSTRACT

This study was undertaken to evaluate the role of progesterone (P4) in modulation of the expression profile of adhesion-related molecules in uterine epithelial cells (UECs) and in vitro blastocyst production in buffalo. UECs were isolated from slaughterhouse-derived uteri by enzymatic treatment, and cells were characterized by immunocytochemistry (ICC) and PCR assays. The well-characterized UECs were exposed to different concentrations of P4 (0, 0.314, 3.14 and 6.28 ng/ml) along with the basal level of oestradiol for 6 days. Thereafter, the relative mRNA expression of different biomolecules such as mucin 1 (MUC1), osteopontin, integrin alpha (α3, α6 and αV) and beta (ß1 and ß3) subunits, progesterone receptor (PR) and oestrogen receptor, was evaluated. Further, day 2 post-insemination embryos were cultured in mSOF supplemented with or without P4. UECs were found positive for cytokeratin expression and negative for vimentin expression. Progesterone treatment significantly enhanced the mRNA expression of most of the transcripts compared with the control group, and correspondingly, the immunofluorescence depicted higher protein expression of all these molecules. Further, the long-term exposure of UECs to P4 downregulated the expression of PR and, concomitantly, MUC1. Progesterone supplementation to embryo culture medium significantly (p < .05) improved the blastocyst rate. The study demonstrates the role of P4 hormone in modulation of the expression of early implantation-related biomolecules in uterine epithelial cells; hence, adequate level of steroids is crucial for normal embryo development and its implantation.


Subject(s)
In Vitro Oocyte Maturation Techniques/veterinary , Progesterone/pharmacology , Uterus/drug effects , Animals , Blastocyst , Buffaloes , Cells, Cultured , Embryo, Mammalian/drug effects , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Female , Integrins/genetics , Integrins/metabolism , Mucin-1/genetics , Mucin-1/metabolism , Osteopontin/genetics , Osteopontin/metabolism , RNA, Messenger/metabolism , Uterus/cytology , Uterus/metabolism
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