Department of Neurosciences, University of California, San Diego, School of Medicine, La Jolla, California 92093-0624, USA.
J Neurosci. 2010 May 5;30(18):6236-46. doi: 10.1523/JNEUROSCI.0567-10.2010.
Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by striatonigral degeneration and olivo-pontocerebellar atrophy. Neuronal degeneration is accompanied by primarily oligodendrocytic accumulation of alpha-synuclein (alphasyn) as opposed to the neuronal inclusions more commonly found in other alpha-synucleinopathies such as Parkinson's disease. It is unclear how alphasyn accumulation in oligodendrocytes may lead to the extensive neurodegeneration observed in MSA; we hypothesize that the altered expression of oligodendrocyte-derived neurotrophic factors by alphasyn may be involved. In this context, the expression of a number neurotrophic factors reportedly expressed by oligodendrocytes [glial-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), and insulin-like growth factor 1 (IGF-1), as well as basic fibroblast growth factor 2 (bFGF2), reportedly astrocyte derived] were examined in transgenic mouse models expressing human alphasyn (halphasyn) under the control of either neuronal (PDGFbeta or mThy1) or oligodendrocytic (MBP) promoters. Although protein levels of BDNF and IGF-1 were altered in all the alphasyn transgenic mice regardless of promoter type, a specific decrease in GDNF protein expression was observed in the MBP-halphasyn transgenic mice. Intracerebroventricular infusion of GDNF improved behavioral deficits and ameliorated neurodegenerative pathology in the MBP-halphasyn transgenic mice. Consistent with the studies in the MBP-halphasyn transgenic mice, analysis of GDNF expression levels in human MSA samples demonstrated a decrease in the white frontal cortex and to a lesser degree in the cerebellum compared with controls. These results suggest a mechanism in which alphasyn expression in oligodendrocytes impacts on the trophic support provided by these cells for neurons, perhaps contributing to neurodegeneration.
多系统萎缩症(MSA)是一种神经退行性疾病,其特征是纹状体黑质变性和橄榄脑桥小脑萎缩。神经元变性伴随着主要是少突胶质细胞中α-突触核蛋白(α-syn)的积累,而不是在其他α-突触核蛋白病中更常见的神经元包涵体,如帕金森病。目前尚不清楚少突胶质细胞中α-syn 的积累如何导致 MSA 中观察到的广泛神经退行性变;我们假设α-syn 改变少突胶质细胞衍生的神经营养因子的表达可能与此有关。在这种情况下,研究了一些据报道由少突胶质细胞表达的神经营养因子[胶质细胞源性神经营养因子(GDNF)、脑源性神经营养因子(BDNF)和胰岛素样生长因子 1(IGF-1),以及碱性成纤维细胞生长因子 2(bFGF2),据报道由星形胶质细胞衍生]在表达人α-syn(α-syn)的转基因小鼠模型中的表达情况,α-syn 的表达受神经元(PDGFβ或 mThy1)或少突胶质细胞(MBP)启动子的控制。尽管无论启动子类型如何,所有α-syn 转基因小鼠的 BDNF 和 IGF-1 蛋白水平都发生了改变,但在 MBP-α-syn 转基因小鼠中观察到 GDNF 蛋白表达的特异性下降。脑室内输注 GDNF 可改善 MBP-α-syn 转基因小鼠的行为缺陷并改善神经退行性病变。与 MBP-α-syn 转基因小鼠的研究一致,对人类 MSA 样本中 GDNF 表达水平的分析表明,与对照组相比,白色额皮质中的 GDNF 表达水平降低,小脑的程度较小。这些结果表明,α-syn 在少突胶质细胞中的表达会影响这些细胞为神经元提供的营养支持的机制,这可能导致神经退行性变。