Intercellular communication via exosomes: A new paradigm in the pathophysiology of neurodegenerative disorders

IF 5.1 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Life sciences Pub Date : 2025-03-15 Epub Date: 2025-02-13 DOI:10.1016/j.lfs.2025.123468
Kiran S. Satao, Gaurav M. Doshi
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Abstract

Neurodegenerative disorders are one of the leading causes of death and disability and pose a great economic burden on healthcare systems. Generally, these neurodegenerative disorders have a progressive deterioration in neural function and structure, and deposition of misfolded proteins commonly occurs, such as amyloid-β in AD and α-synuclein in PD. However, there exists a special class of exosomes, which acts like a transmitter and enhances communication between cells. The present review discusses the significant role of exosomes in neurodegenerative diseases, with a focus on Amyotrophic lateral Sclerosis (ALS), AD, PD, and Huntington's disease (HD). In this review, the biogenesis of exosomes is discussed from multivesicular bodies and onwards to their release into the extracellular environment. The present review focuses on recent data concerning the possible use of modified exosomes as ND therapy. Indeed, future work is needed to explain the processes driving exosome biogenesis and cargo selection, while opening new routes by the use of exosome-based therapeutics in neurodegenerative disease diagnosis and treatment.

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通过外泌体的细胞间通讯:神经退行性疾病病理生理学的新范式
神经退行性疾病是导致死亡和残疾的主要原因之一,并对卫生保健系统造成巨大的经济负担。一般来说,这些神经退行性疾病的神经功能和结构进行性恶化,通常会发生错误折叠蛋白的沉积,如AD的淀粉样蛋白-β和PD的α-突触核蛋白。然而,存在一类特殊的外泌体,它的作用就像一个传递器,增强细胞之间的通信。本文综述了外泌体在神经退行性疾病中的重要作用,重点讨论了肌萎缩性侧索硬化症(ALS)、AD、PD和亨廷顿病(HD)。在这篇综述中,外泌体的生物发生从多泡体和它们释放到细胞外环境进行了讨论。目前的综述集中在最近的数据可能使用修饰外泌体作为ND治疗。事实上,未来的工作需要解释驱动外泌体生物发生和货物选择的过程,同时通过使用基于外泌体的治疗方法在神经退行性疾病的诊断和治疗中开辟新的途径。
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来源期刊
Life sciences
Life sciences 医学-药学
CiteScore
12.20
自引率
1.60%
发文量
841
审稿时长
6 months
期刊介绍: Life Sciences is an international journal publishing articles that emphasize the molecular, cellular, and functional basis of therapy. The journal emphasizes the understanding of mechanism that is relevant to all aspects of human disease and translation to patients. All articles are rigorously reviewed. The Journal favors publication of full-length papers where modern scientific technologies are used to explain molecular, cellular and physiological mechanisms. Articles that merely report observations are rarely accepted. Recommendations from the Declaration of Helsinki or NIH guidelines for care and use of laboratory animals must be adhered to. Articles should be written at a level accessible to readers who are non-specialists in the topic of the article themselves, but who are interested in the research. The Journal welcomes reviews on topics of wide interest to investigators in the life sciences. We particularly encourage submission of brief, focused reviews containing high-quality artwork and require the use of mechanistic summary diagrams.
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