Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, Florida, United States of America.
PLoS One. 2022 Aug 11;17(8):e0272511. doi: 10.1371/journal.pone.0272511. eCollection 2022.
Mitochondrial dysfunction is a hallmark of neurodegeneration. The expression level of Tom40, a crucial mitochondrial membrane protein, is significantly reduced in neurodegenerative disease subjects. Tom40 overexpression studies have shown to protect the neurons against oxidative stress by improving mitochondrial function. Thus, successful delivery of Tom40 protein to the brain could lead to a novel therapy for neurodegenerative diseases. However, delivering protein to the cell may be difficult. Especially the blood-brain barrier (BBB) is a big hurdle to clear in order to deliver the protein to the brain. In the current study, we engineered exosomes, which are the extracellular vesicles of endosomal origin, and able to cross BBB as delivery vehicles packing human Tom40. We found Tom40 protein delivery by the exosome successfully protected the cells against hydrogen peroxide-induced oxidative stress. This result suggests that exosome-mediated delivery of Tom40 may potentially be useful in restoring mitochondrial functions and alleviating oxidative stress in neurodegenerative diseases, such as Alzheimer's and Parkinson's diseases.
线粒体功能障碍是神经退行性变的一个标志。在神经退行性疾病患者中,一种关键的线粒体膜蛋白 Tom40 的表达水平显著降低。Tom40 过表达研究表明,通过改善线粒体功能可以保护神经元免受氧化应激。因此,成功将 Tom40 蛋白递送到大脑可能为神经退行性疾病提供一种新的治疗方法。然而,将蛋白质递送到细胞可能很困难。特别是血脑屏障(BBB)是一个很大的障碍,需要克服才能将蛋白质递送到大脑。在本研究中,我们设计了外泌体,这是内体起源的细胞外囊泡,能够作为携带人 Tom40 的递送载体穿过血脑屏障。我们发现,外泌体介导的 Tom40 蛋白递送成功地保护了细胞免受过氧化氢诱导的氧化应激。这一结果表明,外泌体介导的 Tom40 递送达可能在恢复线粒体功能和缓解神经退行性疾病(如阿尔茨海默病和帕金森病)中的氧化应激方面具有潜在的应用价值。