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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Regulation of alpha-synuclein by bFGF in cultured ventral midbrain dopaminergic neurons.
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Regulation of alpha-synuclein by bFGF in cultured ventral midbrain dopaminergic neurons.

机译:bFGF在培养的腹侧中脑多巴胺能神经元中对α-突触核蛋白的调节。

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Alpha-synuclein is a neuronal protein that is implicated in the control of synaptic vesicle function and in Parkinson's disease (PD). Consequently, alterations of alpha-synuclein levels may play a role in neurotransmission and in PD pathogenesis. However, the factors that regulate alpha-synuclein levels are unknown. Growth factors mediate neurotrophic and plasticity effects in CNS neurons, and may play a role in disease states. Here we examine the regulation of alpha-synuclein levels in primary CNS neurons, with particular emphasis on dopaminergic neurons. E18 rat cortical neurons and dopaminergic neurons of E14 rat ventral midbrain showed an induction of alpha-synuclein protein levels with maturation in culture. Application of basic Fibroblast growth factor (bFGF) promoted alpha-synuclein expression selectively within dopaminergic, and not GABAergic or cortical neurons. This induction was blocked by actinomycin D, but not by inhibition of bFGF-induced glial proliferation. alpha-Synuclein levels were not altered by glial-derived neurotrophic factor (GDNF), or by apoptotic stimuli. We conclude that bFGF promotes alpha-synuclein expression in cultured ventral midbrain dopaminergic neurons through a direct transcriptional effect. These results suggest that distinct growth factors may thus mediate plasticity responses or influence disease states in ventral midbrain dopaminergic neurons.
机译:α-突触核蛋白是一种神经元蛋白,与突触小泡功能的控制和帕金森氏病(PD)有关。因此,α-突触核蛋白水平的改变可能在神经传递和PD发病机理中起作用。但是,调节α-突触核蛋白水平的因素尚不清楚。生长因子介导中枢神经系统神经元的神经营养和可塑性作用,并可能在疾病状态中起作用。在这里,我们研究了主要中枢神经系统神经元中α-突触核蛋白水平的调节,特别强调了多巴胺能神经元。 E18大鼠腹中脑的E18大鼠皮层神经元和多巴胺能神经元在培养中随着成熟而显示出α-突触核蛋白蛋白水平的诱导。碱性成纤维细胞生长因子(bFGF)的应用选择性地促进了多巴胺能而不是GABA能或皮质神经元内的α-突触核蛋白表达。该诱导被放线菌素D阻断,但不被bFGF诱导的神经胶质增生抑制。胶质细胞源性神经营养因子(GDNF)或凋亡刺激不会改变α-突触核蛋白的水平。我们得出结论,bFGF通过直接转录作用促进培养的腹侧中脑多巴胺能神经元中的α-突触核蛋白表达。这些结果表明,不同的生长因子可能因此介导腹侧中脑多巴胺能神经元的可塑性反应或影响疾病状态。

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