Insights on the Characteristics and Therapeutic Potential of Mesenchymal Stem Cell-derived Exosomes for Mitigation of Alzheimer's Disease's Pathogenicity: A Systematic Review.

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Biophysics Pub Date : 2024-10-22 DOI:10.1007/s12013-024-01598-x
Sarah Mohammed Yousuf Abdi, Siti Sarah Mustaffa Al-Bakri, Norshariza Nordin
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Abstract

Alzheimer's disease (AD) remains a progressive neurodegenerative disease with no cure. Treatment of AD relies on administering drugs that only subside the symptoms. In recent studies, mesenchymal stem cell (MSC)-exosomes have been marked to possess therapeutic potential for treating AD. This study aims to systematically review and analyse findings that focus on the isolation, characterisation, and sources of MSC-derived exosomes used to unravel the therapeutic potential of these exosomes targeting AD using in vitro and in vivo models. It is hypothesised that MSC-exosomes exhibit high therapeutic potential for AD treatment by exerting various modes of action. PubMed, Scopus, and Medline were used to find relevant published works from January 2016 until December 2020, using assigned keywords including "Alzheimer's disease", "secretome", and "exosomes". Only research articles meeting the predefined inclusion/exclusion criteria were selected and analysed. The risk of bias was assessed using the Office of Health Assessment and Translation tool (OHAT). A total of 17 eligible in vivo and in vitro studies were included in this review. Bone marrow-derived stem cells (BMSCs) were the most used source for exosome isolation, even though studies on exosomes from adipose-derived stem cells (ADSCs) and human umbilical cord stem cells (HUCSCs) provide more information on the characteristics. When the risk of bias was assessed, the studies presented various levels of biases. Notably, the in vitro and in vivo studies revealed neuroprotective properties of MSC-exosomes through different modes of action to alleviate AD pathology. Our review discovered that most MSC exosomes could degrade Aβ plaques, enhance neurogenesis, extenuate neuroinflammatory response through microglial activation, regulate apoptosis and reduce oxidative stress. Delivery of exosomal micro-RNAs was also found to reduce neuroinflammation. Findings from this review provided convincing systematic evidence highlighting the therapeutic properties of MSC-derived exosomes as a prospective source for cell-free (acellular) therapy in treating AD.

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间充质干细胞衍生的外泌体在缓解阿尔茨海默病致病性方面的特点和治疗潜力:系统综述。
阿尔茨海默病(AD)仍然是一种无法治愈的渐进性神经退行性疾病。治疗阿尔茨海默病的药物只能缓解症状。在最近的研究中,间充质干细胞(MSC)外泌体被证实具有治疗阿尔茨海默病的潜力。本研究旨在系统回顾和分析有关间充质干细胞外泌体的分离、特征和来源的研究结果,并利用体外和体内模型揭示这些外泌体针对AD的治疗潜力。研究假设间充质干细胞外泌体通过发挥不同的作用模式,显示出治疗AD的巨大潜力。研究人员使用 PubMed、Scopus 和 Medline 查找了 2016 年 1 月至 2020 年 12 月期间发表的相关文章,并指定了包括 "阿尔茨海默病"、"分泌组 "和 "外泌体 "在内的关键词。只有符合预定义纳入/排除标准的研究文章才会被选中并进行分析。使用健康评估与转化办公室工具(OHAT)对偏倚风险进行了评估。共有 17 项符合条件的体内和体外研究被纳入本综述。骨髓干细胞(BMSCs)是最常用的外泌体分离来源,尽管有关脂肪干细胞(ADSCs)和人脐带干细胞(HUCSCs)外泌体的研究提供了更多有关其特征的信息。在评估偏倚风险时,各项研究都存在不同程度的偏倚。值得注意的是,体外和体内研究揭示了间充质干细胞外泌体通过不同作用模式缓解AD病理的神经保护特性。我们的综述发现,大多数间充质干细胞外泌体可以降解Aβ斑块、促进神经发生、通过激活微胶质细胞减轻神经炎症反应、调节细胞凋亡和减少氧化应激。研究还发现,外泌体微型核糖核酸的传递也能减轻神经炎症。本综述的研究结果提供了令人信服的系统性证据,强调了间充质干细胞衍生外泌体作为无细胞(细胞)疗法治疗AD的潜在来源的治疗特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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