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神经胶质细胞吞噬作用在阿尔茨海默病中发生改变。

Neuron-astrocyte transmitophagy is altered in Alzheimer's disease.

机构信息

A. I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Finland.

Department of Pharmacology & Therapeutics, University of Melbourne, Australia.

出版信息

Neurobiol Dis. 2022 Aug;170:105753. doi: 10.1016/j.nbd.2022.105753. Epub 2022 May 13.

Abstract

Under physiological conditions in vivo astrocytes internalize and degrade neuronal mitochondria in a process called transmitophagy. Mitophagy is widely reported to be impaired in neurodegeneration but it is unknown whether and how transmitophagy is altered in Alzheimer's disease (AD). Here we report that the internalization of neuronal mitochondria is significantly increased in astrocytes isolated from AD mouse brains. We also demonstrate that the degradation of neuronal mitochondria by astrocytes is increased in AD mice at the age of 6 months onwards. Furthermore, we demonstrate for the first time a similar phenomenon between human neurons and AD astrocytes, and in murine hippocampi in vivo. The results suggest the involvement of S100a4 in impaired mitochondrial transfer between neurons and AD astrocytes together with significant increases in the mitophagy regulator and reactive oxygen species in aged AD astrocytes. These findings demonstrate altered neuron-supporting functions of AD astrocytes and provide a starting point for studying the molecular mechanisms of transmitophagy in AD.

摘要

在体内生理条件下,星形胶质细胞通过一种称为转噬(transmitophagy)的过程内化和降解神经元线粒体。转噬在神经退行性疾病中被广泛报道受损,但尚不清楚转噬在阿尔茨海默病(AD)中是否以及如何发生改变。在这里,我们报告说,从 AD 小鼠大脑中分离出的星形胶质细胞中神经元线粒体的内化显著增加。我们还证明,AD 小鼠在 6 个月龄及以上时,星形胶质细胞对神经元线粒体的降解增加。此外,我们首次在人类神经元和 AD 星形胶质细胞之间以及体内的鼠海马中证明了类似的现象。结果表明,S100a4 参与了神经元和 AD 星形胶质细胞之间受损的线粒体转移,同时 aged AD 星形胶质细胞中的线粒体自噬调节剂和活性氧显著增加。这些发现表明 AD 星形胶质细胞支持神经元的功能发生改变,并为研究 AD 中转噬的分子机制提供了起点。

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