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鉴定帕金森病 6-OHDA 大鼠模型中 TID1 表达的双侧变化。

Identification of bilateral changes in TID1 expression in the 6-OHDA rat model of Parkinson's disease.

机构信息

Hotchkiss Brain Institute, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada.

出版信息

PLoS One. 2011;6(10):e26045. doi: 10.1371/journal.pone.0026045. Epub 2011 Oct 7.

Abstract

Parkinson's disease (PD) is a common neurodegenerative disease characterized by the loss of dopaminergic neurons in the substantia nigra and the aggregation of α-synuclein into Lewy bodies. Existing therapies address motor dysfunction but do not halt progression of the disease. A still unresolved question is the biochemical pathway that modulates the outcome of protein misfolding and aggregation processes in PD. The molecular chaperone network plays an important defensive role against cellular protein misfolding and has been identified as protective in experimental models of protein misfolding diseases like PD. Molecular mechanisms underlying chaperone-neuroprotection are actively under investigation. Current evidence implicates a number of molecular chaperones in PD including Hsp25, Hsp70 and Hsp90, however their precise involvement in the neurodegenerative cascade is unresolved. The J protein family (DnaJ or Hsp40 protein family) has long been known to be important in protein conformational processes.We assessed sensory and motor function of control and PD rats and then evaluated the brain region-specific expression levels of select J proteins by Western analysis. Surprisingly, we observed a widespread 26 kDa breakdown product of the J protein, TID1, (tumorous imaginal discs, mtHsp40 or DnaJ3) in a 6-hydroxydopamine (6-OHDA) rat model of PD in which food handling, gait symmetry and sensory performance were impaired. Greater behavioral deficits were associated with lower TID1 expression. Furthermore, direct application of either 6-OHDA or MPP+ (1-methyl-4-phenylpyridinum) to CAD (CNS-derived catecholinaminergic neuronal cell line) cell cultures, reduced TID1 expression levels.Our results suggest that changes in cellular TID1 are a factor in the pathogenesis of PD by impeding functional and structural compensation and exaggerating neurodegenerative processes. In contrast, no changes were observed in CSPα, Hsp40, Hsp70, Hsc70 and PrP(C) levels and no activation of caspase3 was observed. This study links TID1 to PD and provides a new target for therapeutics that halts the PD progression.

摘要

帕金森病(PD)是一种常见的神经退行性疾病,其特征是黑质中的多巴胺能神经元丧失和α-突触核蛋白聚集成路易体。现有的治疗方法针对运动功能障碍,但不能阻止疾病的进展。一个尚未解决的问题是调节 PD 中蛋白质错误折叠和聚集过程结果的生化途径。分子伴侣网络在对抗细胞蛋白质错误折叠方面发挥着重要的防御作用,并已被确定在 PD 等蛋白质错误折叠疾病的实验模型中具有保护作用。分子伴侣-神经保护的分子机制正在积极研究中。目前的证据表明,许多分子伴侣参与了 PD,包括 Hsp25、Hsp70 和 Hsp90,但它们在神经退行性级联反应中的精确参与仍未得到解决。J 蛋白家族(DnaJ 或 Hsp40 蛋白家族)长期以来一直被认为在蛋白质构象过程中很重要。我们评估了对照组和 PD 大鼠的感觉和运动功能,然后通过 Western 分析评估了选择的 J 蛋白在脑区的特异性表达水平。令人惊讶的是,我们观察到一种广泛存在的 26kDa J 蛋白 TID1(肿瘤想象盘,mtHsp40 或 DnaJ3)的降解产物,在 6-羟多巴胺(6-OHDA)诱导的 PD 大鼠模型中,该模型的食物处理、步态对称性和感觉性能受损。更大的行为缺陷与更低的 TID1 表达有关。此外,直接向 CAD(中枢神经系统衍生的儿茶酚胺能神经元细胞系)细胞培养物中应用 6-OHDA 或 MPP+(1-甲基-4-苯基吡啶),降低了 TID1 的表达水平。我们的研究结果表明,细胞内 TID1 的变化是 PD 发病机制的一个因素,它阻碍了功能和结构的代偿作用,并加剧了神经退行性过程。相比之下,CSPα、Hsp40、Hsp70、Hsc70 和 PrP(C)水平没有变化,也没有观察到 caspase3 的激活。这项研究将 TID1 与 PD 联系起来,并为阻止 PD 进展的治疗提供了一个新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/357f/3189242/1ea421ea850b/pone.0026045.g001.jpg

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