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帕金森病伴和不伴痴呆患者的α-和β-突触核蛋白表达。

Alpha- and beta-synuclein expression in Parkinson disease with and without dementia.

机构信息

Servicio de Anatomía Patológica, Hospital Universitario Germans Trias i Pujol, Universidad Autonoma de Barcelona, Spain.

出版信息

J Neurol Sci. 2011 Nov 15;310(1-2):112-7. doi: 10.1016/j.jns.2011.05.049. Epub 2011 Jun 17.

Abstract

Parkinson disease (PD) is the most important movement disorder and about 50% of patients develop dementia over the time. PD belongs to the group of Lewy body disorders. Alpha-synuclein (AS) is the main component of Lewy bodies and its aggregation is a key event in the pathogenesis of PD. Beta-synuclein (BS) inhibits AS aggregation in vitro and in vivo and has been shown to interact directly with AS regulating its functionality and preventing its oligomerization. Recently, we have described a molecular subgroup of DLB characterized by the drastic BS reduction in cortical areas. In this study we have analyzed the expression of two BS transcripts and the main AS transcript SNCA140, in frozen samples of three brain areas, temporal cortex, caudate nucleus and pons, from patients with PD and PDD in comparison with controls. Relative mRNA expression was determined by real-time PCR with SybrGreen, neuron-specific-enolase as housekeeping gene and the deltadeltaCt method. The most important difference in BS and AS mRNA expression between PD and PDD was found in the caudate nucleus, where BS mRNA was overexpressed in PD and AS mRNA diminished in PDD. Our findings provide new insights into the pathogenesis of dementia in PD, indicating that differential BS and AS expression in the caudate nucleus may represent one of the molecular mechanisms involved in these complex diseases.

摘要

帕金森病(PD)是最重要的运动障碍疾病,约有 50%的患者随着时间的推移会发展为痴呆症。PD 属于路易体障碍的一种。α-突触核蛋白(AS)是路易体的主要成分,其聚集是 PD 发病机制中的一个关键事件。β-突触核蛋白(BS)在体外和体内均能抑制 AS 的聚集,并已被证明能直接与 AS 相互作用,调节其功能并阻止其寡聚化。最近,我们描述了一种以皮质区域 BS 急剧减少为特征的 DLB 分子亚群。在这项研究中,我们分析了三个脑区(颞叶皮层、尾状核和脑桥)的冷冻样本中两种 BS 转录本和主要 AS 转录本 SNCA140 在 PD 和 PDD 患者中的表达情况,并与对照组进行了比较。采用实时 PCR 结合 SybrGreen、神经元特异性烯醇化酶作为管家基因和 deltadeltaCt 法测定相对 mRNA 表达。BS 和 AS mRNA 在 PD 和 PDD 之间的表达差异最显著的是在尾状核,BS mRNA 在 PD 中过度表达,而 AS mRNA 在 PDD 中减少。我们的研究结果为 PD 痴呆的发病机制提供了新的见解,表明尾状核中 BS 和 AS 表达的差异可能是这些复杂疾病相关的分子机制之一。

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