Dhapola Rishika, Kumari Sneha, Sharma Prajjwal, Paidlewar Mohit, Medhi Bikash, Vellingiri Balachandar, HariKrishnaReddy Dibbanti
Advanced Pharmacology and Neuroscience Laboratory, Department of Pharmacology, School of Health Sciences, Central University of Punjab, Ghudda, Bathinda, 151401, Punjab, India.
Department of Pharmacology, Post Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Mol Neurobiol. 2025 Jul 18. doi: 10.1007/s12035-025-05216-6.
The rapidly growing aging population and increasing risk of Alzheimer's disease (AD) necessitate the development of more effective therapeutic strategies. Extracellular vesicles (EVs) have emerged as a promising therapeutic avenue for AD. EVs, including exosomes, microvesicles, and apoptotic bodies, are lipid bilayer-enclosed particles secreted by various cells that mediate intercellular communication through the transfer of proteins, lipids, RNA, and other bioactive molecules. EVs have various advantages over traditional therapeutic strategies, including high bioavailability, exceptional biocompatibility, and low immunogenicity. There are various methods for extraction and isolation of EVs to ensure reproducibility and characterization. Amyloid plaque formation, tau hyperphosphorylation, neuroinflammation, oxidative stress, and synaptic loss in AD are efficiently ameliorated using EVs. Moreover, signaling pathways are reported to be altered in AD, which have also been found to be regulated by EVs to promote neuronal growth and survival, including NFκB, MAPK, NLRP3, Nrf2/Keap1, HO-1, and TFAM. Preclinical studies have demonstrated that EVs derived from various sources, including mesenchymal stem cells (MSCs), neural stem cells (NSCs), and immune cells, can attenuate AD pathology by reducing amyloid-β (Aβ) accumulation, mitigating tau hyperphosphorylation, enhancing autophagy, and promoting synaptic plasticity. EV-based therapies for AD are in early clinical evaluation, with ongoing trials assessing their safety and efficacy. Key challenges include dosing, biodistribution, large-scale production, and immune responses. Despite these hurdles, EVs offer a promising, non-invasive alternative to stem cell therapy with lower risks and improved targeting potential.
人口老龄化迅速加剧以及阿尔茨海默病(AD)风险不断增加,使得开发更有效的治疗策略成为必要。细胞外囊泡(EVs)已成为治疗AD的一条有前景的途径。EVs包括外泌体、微囊泡和凋亡小体,是由各种细胞分泌的脂质双分子层包裹的颗粒,通过蛋白质、脂质、RNA和其他生物活性分子的传递介导细胞间通讯。与传统治疗策略相比,EVs具有多种优势,包括高生物利用度、出色的生物相容性和低免疫原性。有多种提取和分离EVs的方法以确保可重复性和特性鉴定。使用EVs可有效改善AD中的淀粉样斑块形成、tau蛋白过度磷酸化、神经炎症、氧化应激和突触丧失。此外,据报道AD中的信号通路发生了改变,也发现这些信号通路受EVs调节以促进神经元生长和存活,包括NFκB、MAPK、NLRP3、Nrf2/Keap1、HO-1和TFAM。临床前研究表明,源自多种来源的EVs,包括间充质干细胞(MSCs)、神经干细胞(NSCs)和免疫细胞,可通过减少淀粉样β蛋白(Aβ)积累、减轻tau蛋白过度磷酸化、增强自噬和促进突触可塑性来减轻AD病理。基于EVs的AD治疗正处于早期临床评估阶段,正在进行的试验评估其安全性和有效性。关键挑战包括给药剂量、生物分布、大规模生产和免疫反应。尽管存在这些障碍,但EVs提供了一种有前景的、非侵入性的替代干细胞治疗方法且风险更低、靶向潜力更高。