Howitt Jason, Hill Andrew F
From the Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, Victoria 3010 and
the Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, La Trobe University, Bundoora, Victoria 3086, Australia
J Biol Chem. 2016 Dec 23;291(52):26589-26597. doi: 10.1074/jbc.R116.757955. Epub 2016 Nov 16.
More than 30 years ago, two unexpected findings were discovered that challenged conventional thinking in biology. The first was the identification of a misfolded protein with transmissible properties associated with a group of neurodegenerative diseases known as transmissible spongiform encephalopathies. The second was the discovery of a new pathway used for the extracellular release of biomolecules, including extracellular vesicles called exosomes. Two decades later, the convergence of these pathways was shown when exosomes were found to play a significant role in both the transmission and propagation of protein aggregates in disease. Recent research has now revealed that the majority of proteins involved in neurodegenerative diseases are transported in exosomes, and that external stresses due to age-related impairment of protein quality control mechanisms can promote the transcellular flux of these proteins in exosomes. Significantly, exosomes provide an environment that can induce the conformational conversion of native proteins into aggregates that can be transmitted to otherwise aggregate-free cells in the brain. Here we review the current roles of exosomes in the pathology of neurodegenerative diseases.
30多年前,人们发现了两个意想不到的结果,它们挑战了生物学中的传统思维。第一个是鉴定出一种具有可传播特性的错误折叠蛋白,它与一组被称为传染性海绵状脑病的神经退行性疾病有关。第二个是发现了一种用于生物分子细胞外释放的新途径,包括被称为外泌体的细胞外囊泡。二十年后,当发现外泌体在疾病中蛋白质聚集体的传播和扩散中起重要作用时,这些途径的交汇点得以显现。最近的研究表明,大多数与神经退行性疾病相关的蛋白质是通过外泌体运输的,并且由于与年龄相关的蛋白质质量控制机制受损而产生的外部压力可以促进这些蛋白质在外泌体中的跨细胞通量。值得注意的是,外泌体提供了一个环境,能够诱导天然蛋白质构象转变为聚集体,这些聚集体可以传播到大脑中原本不含聚集体的细胞。在此,我们综述了外泌体在神经退行性疾病病理学中的当前作用。