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评估 TorsinA 作为治疗帕金森病的靶点在小鼠模型中的作用。

Evaluation of TorsinA as a target for Parkinson disease therapy in mouse models.

机构信息

Center for Neurodegeneration and Experimental Therapeutics, Department of Neurology, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.

出版信息

PLoS One. 2012;7(11):e50063. doi: 10.1371/journal.pone.0050063. Epub 2012 Nov 21.

Abstract

Parkinson disease (PD) is a common and disabling disorder. No current therapy can slow or reverse disease progression. An important aspect of research in this field is target validation, a systematic approach to evaluating the likelihood that modification of a certain molecule, mechanism or biological pathway may be useful for the development of pharmacological or molecular treatments for the disease. TorsinA, a member of the AAA+ family of chaperone proteins, has been proposed as a potential target of neuroprotective therapy. TorsinA is found in Lewy bodies in human PD, and can suppress toxicity in cellular and invertebrate models of PD. Here, we evaluated the neuroprotective properties of torsinA in mouse models of PD based on intoxication with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) as well as recombinant adeno associated virus (rAAV) induced overexpression of alpha-synuclein (α-syn). Using either transgenic mice with overexpression of human torsinA (hWT mice) or mice in which torsinA expression was induced using an rAAV vector, we found no evidence for protection against acute MPTP intoxication. Similarly, genetic deletion of the endogenous mouse gene for torsinA (Dyt1) using an rAAV delivered Cre recombinase did not enhance the vulnerability of dopaminergic neurons to MPTP. Overexpression of α-syn using rAAV in the mouse substantia nigra lead to a loss of TH positive neurons six months after administration, and no difference in the degree of loss was observed between transgenic animals expressing forms of torsinA and wild type controls. Collectively, we did not observe evidence for a protective effect of torsinA in the mouse models we examined. Each of these models has limitations, and there is no single model with established predictive value with respect to the human disease. Nevertheless, these data do seem to support the view that torsinA is unlikely to be successfully translated as a target of therapy for human PD.

摘要

帕金森病(PD)是一种常见且致残的疾病。目前尚无任何疗法能够减缓或逆转疾病进展。该领域研究的一个重要方面是靶标验证,这是一种系统的方法,用于评估改变特定分子、机制或生物途径是否可能对开发治疗该疾病的药理学或分子疗法有用。TorsinA 是伴侣蛋白 AAA+家族的成员,它被认为是神经保护治疗的潜在靶标。TorsinA 存在于人类 PD 的路易体中,并且可以在 PD 的细胞和无脊椎动物模型中抑制毒性。在这里,我们评估了基于 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)中毒以及重组腺相关病毒(rAAV)诱导的α-突触核蛋白(α-syn)过表达的 PD 小鼠模型中 torsinA 的神经保护特性。我们使用过表达人 torsinA 的转基因小鼠(hWT 小鼠)或使用 rAAV 载体诱导 torsinA 表达的小鼠,发现没有证据表明其可以对抗急性 MPTP 中毒。同样,使用 rAAV 递送 Cre 重组酶对内源性小鼠 torsinA 基因(Dyt1)进行基因缺失也不会增加多巴胺能神经元对 MPTP 的易感性。使用 rAAV 在小鼠黑质中过表达 α-syn 会导致 TH 阳性神经元在给药后 6 个月丢失,并且在表达 torsinA 形式的转基因动物和野生型对照之间观察到的丢失程度没有差异。总的来说,我们没有在我们检查的小鼠模型中观察到 torsinA 的保护作用的证据。这些模型中的每一个都有其局限性,并且没有一个具有针对人类疾病的既定预测价值的单一模型。然而,这些数据似乎支持 torsinA 不太可能成功转化为治疗人类 PD 的靶标的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f04/3503809/8a771bbfb0f4/pone.0050063.g001.jpg

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