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Progesterone synthesized by Schwann cells during myelin formation regulates neuronal gene expression

机译:雪旺细胞在髓鞘形成过程中合成的孕酮调节神经元基因表达

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Previously, progesterone was found to regulate the initiation and biosynthetic rate of myelin synthesis in Schwann celleuronal cocultures. The mRNA for cytochrome P450scc (converts cholesterol to pregnenolone), 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD, converts pregnenolone to progesterone), and the progesterone receptor were found to be markedly induced during active myelin synthesis. However, the cells in the cocultures responsible for these changes were not identified. In this study, in situ hybridization was used to determine the localization of the enzymes responsible for steroid biosynthesis. The mRNA for cytochrome P450scc and 3 beta-HSD were detected only in actively myelinating cocultures and were localized exclusively in the Schwann cells. Using immunocytochemistry, with minimal staining of the Schwann cells, we found the progesterone receptor in the dorsal root ganglia (DRG) neurons. The progesterone receptor in the neurons translocated into the nuclei of these cells when progesterone was added to neuronal cultures or during myelin synthesis in the cocultures. Additionally, a marked induction of the progesterone receptor was found in neuronal cultures after the addition of progesterone. The induction of various genes in the neurons was also investigated using mRNA differential display PCR in an attempt to elucidate the mechanism of steroid action on myelin synthesis. Two novel genes were induced in neuronal cultures by progesterone. These genes, along with the progesterone receptor, were also induced in cocultures during myelin synthesis, and their induction was blocked by RU-486 (a progesterone receptor antagonist). These genes were not induced in Schwann cells cultured alone after the addition of progesterone. These results suggest that progesterone is synthesized in Schwann cells and that it can indirectly regulate myelin formation by activating transcription via the classical steroid receptor in the DRG neurons. [References: 46]
机译:以前,发现黄体酮可调节雪旺细胞/神经元共培养物中髓磷脂合成的起始和生物合成速率。发现细胞色素P450scc的mRNA(将胆固醇转化为孕烯醇酮),3β-羟基类固醇脱氢酶(3β-HSD,将孕烯醇酮转化为孕酮)和孕激素受体在活跃的髓磷脂合成过程中被显着诱导。然而,共培养中负责这些变化的细胞没有被鉴定。在这项研究中,原位杂交被用来确定负责类固醇生物合成的酶的定位。仅在活跃的髓鞘共培养物中检测到细胞色素P450scc和3 beta-HSD的mRNA,并且仅位于雪旺氏细胞中。使用免疫细胞化学,对雪旺氏细胞染色最少,我们在背根神经节(DRG)神经元中发现了孕酮受体。当将孕酮添加到神经元培养物中或在共培养物中的髓鞘合成期间,神经元中的孕酮受体易位到这些细胞的核中。另外,在添加孕酮后在神经元培养物中发现孕酮受体的显着诱导。还尝试使用mRNA差异显示PCR研究神经元中各种基因的诱导,以阐明类固醇对髓鞘合成的作用机制。孕酮在神经元培养物中诱导了两个新基因。这些基因以及孕激素受体在髓磷脂合成过程中也被共培养诱导,并且它们的诱导被RU-486(孕激素受体拮抗剂)阻断。在添加黄体酮后,单独培养的雪旺细胞中未诱导这些基因。这些结果表明孕激素是在雪旺氏细胞中合成的,它可以通过激活DRG神经元中经典的类固醇受体的转录来间接调节髓磷脂的形成。 [参考:46]

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