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Influence of Interferon-${ au}$ on the Production of Prostaglandins, Cyclooxygenase-2 Expression In Vitro and Release of Progesterone in Bovine Endometrial Cells
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  • Influence of Interferon-${ au}$ on the Production of Prostaglandins, Cyclooxygenase-2 Expression In Vitro and Release of Progesterone in Bovine Endometrial Cells
  • Influence of Interferon-${ au}$ on the Production of Prostaglandins, Cyclooxygenase-2 Expression In Vitro and Release of Progesterone in Bovine Endometrial Cells
저자명
Lee. Ji-Eun,Lee. Yong-Seung,Yoo. Han-Jun,Lee. Kyoung-Jin,Park. Joung-Jun,Cheong. Hee-Tae,Yang. Boo-Keun,Park. Choon-Keun
간행물명
韓國受精卵移植學會誌
권/호정보
2012년|27권 4호|pp.245-252 (8 pages)
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한국수정란이식학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The purpose of the present study was to investigate the effect of IFN-${ au}$ on prostaglandin synthesis, cyclooxygenase-2 (COX-2) gene expression in vitro and concentration of progesterone (P4) in endometrial cells. Epithelial and stromal cells cultured in vitro were isolated from bovine endometrium and stimulated with increasing doses of IFN-${ au}$ (0, 0.02, 0.2 and 2 ug/ml). Human chorionic gonadotropin (hCG, 1.5 IU/ml) was used as a positive control. Prostaglandin $E_2$ and $F_{2{alpha}}$ levels in the culture media were analyzed by enzyme immunoassays and total RNA was extracted from the cells for RT-PCR. P4 concentrations of blood samples were assayed by chemiluminescent immuno assays system. In epithelial cells, COX-2 gene expression was increased in the presence of IFN-${ au}$ (p<0.05), but it was not significantly different in all groups of stromal cells except for 2 ug/ml IFN-${ au}$ group (p<0.05). Although IFN-${ au}$ did not affect $PGE_2$ and $PGF_{2{alpha}}$ production in epithelial cells, it decreased $PGE_2$ and $PGF_{2{alpha}}$ production significantly in stromal cells (p<0.05). In vivo experiment, blood concentration of P4 was significantly increased after addition of IFN-${ au}$ (1 ug/ml). The results indicate that PG production was mediated by COX-2 expression in stromal cells but it was not affected in epithelial cells and this suggest that treatment of IFN-${ au}$ could improve the implantation environment of uterine by maintenance of high P4 concentration.