Suppr超能文献

丹参酮 IIA 通过泛素-蛋白酶体通路特异性降解内源性 Tau 蛋白并抑制 Tau 纤维形成。

Specific Degradation of Endogenous Tau Protein and Inhibition of Tau Fibrillation by Tanshinone IIA through the Ubiquitin-Proteasome Pathway.

机构信息

Shenzhen Key Laboratory of Marine Bioresource and Eco-environmental Science, Guangdong Provincial Key Laboratory for Plant Epigenetics, College of Life Sciences and Oceanography , Shenzhen University , Shenzhen 518060 , PR China.

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering , Shenzhen University , Shenzhen 518060 , PR China.

出版信息

J Agric Food Chem. 2020 Feb 19;68(7):2054-2062. doi: 10.1021/acs.jafc.9b07022. Epub 2020 Feb 7.

Abstract

Alzheimer's disease (AD) is a common neurodegenerative disease which is partly characterized by the aggregation of hyperphosphorylated Tau proteins forming neurofibrillary tangles that promote AD pathogenesis. In this study, we investigated the effects of tanshinone IIA (Tan IIA) isolated from Salvia miltiorrhiza on Tau degradation in the treatment of AD. The results showed that Tan IIA reduced the Tau expression and attenuated Tau phosphorylation in N2a cells, Tau-overexpressing cells, and 3×Tg-AD mouse primary neuron cells. Moreover, Tan IIA increased polyubiquitinated Tau accumulation and induced proteasomal degradation of the Tau protein. Additionally, Tan IIA became bound to the Tau protein and inhibited the formation of heparin-induced Tau fibrils. In summary, Tan IIA can increase polyubiquitinated Tau accumulation and induce the proteasomal degradation of the Tau protein and the binding of Tan IIA to the Tau protein, inhibiting the formation of Tau fibrils. Tan IIA may be further explored as a potential candidate for AD treatment.

摘要

阿尔茨海默病(AD)是一种常见的神经退行性疾病,其部分特征是过度磷酸化的 Tau 蛋白聚集形成神经纤维缠结,从而促进 AD 的发病机制。在这项研究中,我们研究了丹参酮 IIA(Tan IIA)从丹参中分离出来对 AD 治疗中 Tau 降解的影响。结果表明,Tan IIA 降低了 N2a 细胞、过度表达 Tau 的细胞和 3×Tg-AD 小鼠原代神经元细胞中的 Tau 表达,并减弱 Tau 磷酸化。此外,Tan IIA 增加了多聚泛素化 Tau 的积累,并诱导 Tau 蛋白的蛋白酶体降解。此外,Tan IIA 与 Tau 蛋白结合,抑制肝素诱导的 Tau 纤维的形成。总之,Tan IIA 可以增加多聚泛素化 Tau 的积累,并诱导 Tau 蛋白的蛋白酶体降解以及 Tan IIA 与 Tau 蛋白的结合,抑制 Tau 纤维的形成。Tan IIA 可能作为 AD 治疗的潜在候选药物进一步得到探索。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验