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神经退行性疾病中的突触融合蛋白。

Synaptotagmins in neurodegeneration.

机构信息

Medical Faculty, Institute of Pathophysiology, University of Ljubljana, Ljubljana, Slovenia.

出版信息

Anat Rec (Hoboken). 2009 Dec;292(12):1849-62. doi: 10.1002/ar.21026.

Abstract

Synaptotagmins (Syts) are transmembrane proteins involved in the regulation of membrane trafficking. Here, we summarize literature data that provide growing evidence that several Syts are involved in the pathophysiological mechanisms of temporal lobe epilepsy and Parkinson's disease, as well as few reports related to brain ischemia and Alzheimer's disease (AD). We also report new data from our laboratories, showing changes of the expression of several Syts in Tg2576 mouse model of AD that may be related to neuroinflammation surrounding the beta-amyloid plaques. Furthermore, we demonstrate N-methyl-D-aspartate receptor-mediated upregulation of Syt 4 mRNA in a model of excitotoxic striatal lesion induced by unilateral striatal injection of quinolinic acid, associating the upregulation of Syt 4 with mechanisms of excitotoxicity. We propose that pharmacological manipulation of Syt expression in animal models of neurodegeneration should be further explored, as it may help to clarify the role of individual Syt isoforms in the regulation of membrane trafficking in neurodegeneration.

摘要

突触结合蛋白(Syts)是参与膜运输调节的跨膜蛋白。在这里,我们总结了文献数据,这些数据提供了越来越多的证据表明,几种 Syts 参与了颞叶癫痫和帕金森病的病理生理机制,以及与脑缺血和阿尔茨海默病(AD)相关的少数报道。我们还报告了我们实验室的新数据,显示 AD 的 Tg2576 小鼠模型中几种 Syts 的表达变化,这些变化可能与β淀粉样斑块周围的神经炎症有关。此外,我们证明了 N-甲基-D-天冬氨酸受体介导的 Syt 4 mRNA 在单侧纹状体注射喹啉酸诱导的兴奋性纹状体损伤模型中的上调,将 Syt 4 的上调与兴奋性毒性机制联系起来。我们提出,应该进一步探索神经退行性变动物模型中 Syts 表达的药理学操作,因为这可能有助于阐明单个 Syts 同工型在神经退行性变中调节膜运输的作用。

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