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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >GABA synthesis in Schwann cells is induced by the neuroactive steroid allopregnanolone.
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GABA synthesis in Schwann cells is induced by the neuroactive steroid allopregnanolone.

机译:雪旺细胞中的GABA合成是由神经活性类固醇allregregnanolone诱导的。

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Recent evidence showed that neurotransmitters are synthesised in glial cells, such as the Schwann cells, which form myelin sheaths in the PNS. While the presence of GABA type A (GABA-A) receptors has been previously demonstrated in these cells, the evidence of GABA synthesis remained still elusive. In an attempt to demonstrate the presence of GABA in rat Schwann cells, we adopted a strategy, using several integrated neurochemical, molecular as well as immunocytochemical approaches. We first demonstrated the presence of glutamic acid decarboxylase of 67 kDa (GAD67) in Schwann cells, a crucial enzyme of the GABA synthesis mechanism. Second, we demonstrated that GABA is synthesized and localized in Schwann cells. As the third step we showed that allopregnanolone (10 nM), a potent allosteric modulator of GABA-A receptors, stimulates GABA synthesis through increased levels of GAD67 in Schwann cells. Analysis of intracellular signalling mechanisms revealed that the protein kinase A pathway, through enhanced cAMP levels and cAMP response element binding protein phosphorylation, modulates the allosteric action of allopregnanolone at the GABA-A receptor in Schwann cells. Our findings are the first to demonstrate that this GABA mechanism is active in Schwann cells thus establishing new potential therapeutic targets to control Schwann cell biology, which may prove useful in the treatment of several neurodegenerative disorders.
机译:最近的证据表明神经递质是在神经胶质细胞(如雪旺氏细胞)中合成的,它们在PNS中形成髓鞘。尽管先前已在这些细胞中证明了GABA A型(GABA-A)受体的存在,但GABA合成的证据仍然难以捉摸。为了试图证明大鼠雪旺细胞中GABA的存在,我们采用了一种策略,使用了几种整合的神经化学,分子以及免疫细胞化学方法。我们首先证明了在雪旺细胞中67 kDa(GAD67)的谷氨酸脱羧酶的存在,这是GABA合成机制的关键酶。其次,我们证明了GABA是合成的并且位于雪旺氏细胞中。第三步,我们证明了有效的GABA-A受体变构调节剂allopregnanolone(10 nM)通过增加Schwann细胞中GAD67的水平来刺激GABA的合成。细胞内信号转导机制的分析表明,蛋白激酶A途径通过增强cAMP水平和cAMP反应元件结合蛋白磷酸化来调节异戊烷醇对Schwann细胞中GABA-A受体的变构作用。我们的发现首次证明该GABA机制在雪旺氏细胞中具有活性,从而建立了控制雪旺氏细胞生物学的新潜在治疗靶标,这可能被证明可用于治疗多种神经退行性疾病。

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