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Influence of Estradiol-17beta on Progesterone and Estrogen Receptor mRNA Expression in Porcine Follicular Granulosa Cells during Short-Term, In Vitro Real-Time Cell Proliferation

机译:雌二醇-17Beta在短期内猪卵泡颗粒细胞中雌激素和雌激素受体mRNA表达的影响,体外实时细胞增殖

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摘要

Progesterone (P4) and estradiol (E2) play a significant role in mammalian reproduction. Our study demonstrated that separated porcine cumulus cells (CCs) and/or granulosa cells (GCs) might proliferate in vitro during short-term, real-time primary culture. The GCs were analyzed according to gene expression of the progesterone receptor (nuclear form) (pgr), progesterone receptor membrane component 1 (pgrmc1), and estrogen-related receptor beta 3 (esrrb3) in relation to two housekeeping genes: actb and pbgd. GCs were cultivated in medium with the E2. Both pgr/actb and pgr/pbgd revealed higher expression between 24 and 168 h of IVC of prolonged E2 treatment and at 48 h of IVC after acute E2 administration. The pgrmc1/actb and pgrmc1/pbgd displayed increased expression after prolonged E2 treatment between 24 and 120 h of IVC. The highest level of esrrb3/actb at 120 and 144 h, as well as esrrb3/pbgd at 120 h, in untreated controls as compared to the hormone-stimulated group, was observed. We suggest that E2 significantly influences the upregulation of pgr, pgrmc1, and esrrb3 expression in porcine GCs during real-time cell proliferation. Since esrrb3 expression is stimulated by E2 in both an acute and prolonged manner, estradiol may be recognized as a potential estrogen receptor agonist in GCs.
机译:孕酮(P4)和雌二醇(E2)在哺乳动物再现显著的作用。我们的研究表明,分离的猪卵丘细胞(CC)上和/或颗粒细胞(GCS)可能短期,实时原代培养期间在体外增殖。根据孕激素受体(核形式)(PGR),孕酮受体膜成分1(PGRMC1)的基因表达的GC进行分析,并在相对于雌激素相关受体β3(esrrb3)针对两种持家基因:ACTB和PBGD。地方选区与E2培养基中培养。既PGR / ACTB和PGR / PBGD揭示24和延长的E2治疗的IVC的168小时,并在之间的IVC 48小时急性E2给药后更高的表达。所述PGRMC1 / ACTB和PGRMC1 / PBGD显示增长24和IVC 120小时之间延长E2处理后表达。的esrrb3 / ACTB,在120和144小时的最高水平,以及esrrb3 / PBGD在120小时,在相比于激素刺激的组未处理的对照,进行了观察。我们认为,E2显著影响植物生长调节剂,PGRMC1,并在猪的GC esrrb3表达的过程中实时细胞增殖的上调。由于esrrb3表达通过在E2两者急性和延长的方式刺激,雌二醇可以被识别为在GC中,潜在的雌激素受体激动剂。

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