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Engineered Extracellular Vesicles/Exosomes as a New Tool against Neurodegenerative Diseases

机译:工程化的细胞外囊泡/外泌体作为抗神经退行性疾病的新工具

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摘要

Neurodegenerative diseases are commonly generated by intracellular accumulation of misfolded/aggregated mutated proteins. These abnormal protein aggregates impair the functions of mitochondria and induce oxidative stress, thereby resulting in neuronal cell death. In turn, neuronal damage induces chronic inflammation and neurodegeneration. Thus, reducing/eliminating these abnormal protein aggregates is a priority for any anti-neurodegenerative therapeutic approach. Although several antibodies against mutated neuronal proteins have been already developed, how to efficiently deliver them inside the target cells remains an unmet issue. Extracellular vesicles/exosomes incorporating intrabodies against the pathogenic products would be a tool for innovative therapeutic approaches. In this review/perspective article, we identify and describe the major molecular targets associated with neurodegenerative diseases, as well as the antibodies already developed against them. Finally, we propose a novel targeting strategy based on the endogenous engineering of extracellular vesicles/exosomes constitutively released by cells of the central nervous system.
机译:神经退行性疾病通常是由错误折叠/聚集的突变蛋白的细胞内积累而产生的。这些异常的蛋白质聚集体损害线粒体的功能并诱导氧化应激,从而导致神经元细胞死亡。反过来,神经元损伤引起慢性炎症和神经变性。因此,减少/消除这些异常蛋白质聚集体是任何抗神经退行性治疗方法的优先事项。尽管已经开发了几种针对突变神经元蛋白的抗体,但是如何有效地将其递送到靶细胞内仍是一个未解决的问题。掺入针对病原体的体内抗体的细胞外囊泡/外泌体将是创新治疗方法的工具。在这篇综述/观点文章中,我们确定并描述了与神经退行性疾病相关的主要分子靶标,以及针对它们的抗体。最后,我们提出了一种新的靶向策略,该策略基于中枢神经系统细胞组成性释放的细胞外囊泡/外泌体的内源性工程。

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