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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Culture of bovine ovarian follicle wall sections maintained the highly estrogenic profile under basal and chemically defined conditions
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Culture of bovine ovarian follicle wall sections maintained the highly estrogenic profile under basal and chemically defined conditions

机译:在基础和化学条件下,牛卵巢卵泡壁的培养物保持了高度雌激素的分布

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Follicle cultures reproduce in vitro the functional features observed in vivo. In a search for an ideal model, we cultured bovine antral follicle wall sections (FWS) in a serum-free defined medium (DM) known to induce 17β-estradiol (E2) production, and in a nondefined medium (NDM) containing serum. Follicles were sectioned and cultured in NDM or DM for 24 or 48 h. Morphological features were determined by light microscopy. Gene expression of steroidogenic enzymes and follicle-stimulating hormone (FSH) receptor were determined by RT-PCR; progesterone (P4) and E2 concentrations in the media were measured by radioimmunoassay. DM, but not NDM, maintained an FWS morphology in vitro that was similar to fresh tissue. DM also induced an increase in the expression of all steroidogenic enzymes, except FSH receptor, but NDM did not. In both DM and NDM, there was a gradual increase in P4 throughout the culture period; however, P4 concentration was significantly higher in NDM. In both media, E2 concentration was increased at 24 h, followed by a decrease at 48 h. The E2:P4 ratio was higher in DM than in NDM. These results suggest that DM maintains morphological structure, upregulates the expression of steroidogenic enzyme genes, and maintains steroid production with a high E2:P4 ratio in FWS cultures.
机译:卵泡培养物在体外再现体内观察到的功能特征。在寻找理想模型的过程中,我们在已知可诱导17β-雌二醇(E2)产生的无血清定义培养基(DM)以及含有血清的非确定培养基(NDM)中培养了牛窦卵泡壁切片(FWS)。将卵泡切成薄片并在NDM或DM中培养24或48小时。通过光学显微镜确定形态特征。 RT-PCR检测类固醇生成酶和促卵泡激素(FSH)受体的基因表达。通过放射免疫测定法测量培养基中的孕酮(P4)和E2浓度。 DM,但不是NDM,在体外保持与新鲜组织相似的FWS形态。 DM还诱导除FSH受体外的所有类固醇生成酶的表达增加,但NDM却没有。在DM和NDM中,整个培养期间P4都逐渐增加。但是,NDM中的P4浓度明显更高。在两种培养基中,E2浓度均在24 h升高,然后在48 h降低。 DM中的E2:P4比率高于NDM。这些结果表明DM在FWS培养物中维持形态结构,上调类固醇酶基因的表达,并以高E2∶P4比例维持类固醇产生。

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