首页> 美国卫生研究院文献>The Journal of Neuroscience >Synaptic Regulator α-Synuclein in Dopaminergic Fibers Is Essentially Required for the Maintenance of Subependymal Neural Stem Cells
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Synaptic Regulator α-Synuclein in Dopaminergic Fibers Is Essentially Required for the Maintenance of Subependymal Neural Stem Cells

机译:多巴胺能纤维中的突触调节剂α-突触核蛋白是维持表皮下神经干细胞的必要条件。

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摘要

Synaptic protein α-synuclein (α-SYN) modulates neurotransmission in a complex and poorly understood manner and aggregates in the cytoplasm of degenerating neurons in Parkinson′s disease. Here, we report that α-SYN present in dopaminergic nigral afferents is essential for the normal cycling and maintenance of neural stem cells (NSCs) in the brain subependymal zone of adult male and female mice. We also show that premature senescence of adult NSCs into non-neurogenic astrocytes in mice lacking α-SYN resembles the effects of dopaminergic fiber degeneration resulting from chronic exposure to 1-methyl-4-phenyl-1,2,3,6-tetra-hydropyridine or intranigral inoculation of aggregated toxic α-SYN. Interestingly, NSC loss in α-SYN-deficient mice can be prevented by viral delivery of human α-SYN into their sustantia nigra or by treatment with l-DOPA, suggesting that α-SYN regulates dopamine availability to NSCs. Our data indicate that α-SYN, present in dopaminergic nerve terminals supplying the subependymal zone, acts as a niche component to sustain the neurogenic potential of adult NSCs and identify α-SYN and DA as potential targets to ameliorate neurogenic defects in the aging and diseased brain.>SIGNIFICANCE STATEMENT We report an essential role for the protein α-synuclein present in dopaminergic nigral afferents in the regulation of adult neural stem cell maintenance, identifying the first synaptic regulator with an implication in stem cell niche biology. Although the exact role of α-synuclein in neural transmission is not completely clear, our results indicate that it is required for stemness and the preservation of neurogenic potential in concert with dopamine.
机译:突触蛋白α-突触核蛋白(α-SYN)以复杂且鲜为人知的方式调节神经传递,并聚集在帕金森氏病变性神经元的细胞质中。在这里,我们报告多巴胺能黑质传入中存在的α-SYN对于成年雄性和雌性小鼠脑室下膜区的神经干细胞(NSCs)的正常循环和维持至关重要。我们还显示,成年NSC缺乏α-SYN的小鼠过早衰老成非神经源性星形胶质细胞,类似于长期暴露于1-甲基-4-苯基-1,2,3,6-四氢萘酚引起的多巴胺能纤维变性的影响。氢吡啶或鼻内接种聚集的有毒α-SYN。有趣的是,α-SYN缺陷型小鼠的NSC丢失可以通过将人α-SYN病毒递送到黑面病中或通过用1-DOPA处理来预防,这表明α-SYN可以调节NSC的多巴胺利用率。我们的数据表明,存在于提供表皮下区的多巴胺能神经末梢的α-SYN可以作为利基成分来维持成人NSC的神经源性潜力,并确定α-SYN和DA是缓解衰老和患病神经源性缺陷的潜在靶标>重要意义声明:我们报道了多巴胺能黑质传入中存在的α-突触核蛋白蛋白在调节成人神经干细胞维持中的重要作用,从而确定了第一个与干细胞生态位生物学有关的突触调节剂。 。尽管α-突触核蛋白在神经传递中的确切作用尚不完全清楚,但我们的研究结果表明,α-突触核蛋白与多巴胺协同作用是干和保持神经源性潜力所必需的。

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