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间充质基质细胞(MSC)为基础的方法在慢性神经退行性变中的治疗效用:潜在机制、现状和前景一瞥。

Therapeutic utility of mesenchymal stromal cell (MSC)-based approaches in chronic neurodegeneration: a glimpse into underlying mechanisms, current status, and prospects.

机构信息

Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.

Department of Prosthetic Dentistry, I. M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

出版信息

Cell Mol Biol Lett. 2022 Jul 16;27(1):56. doi: 10.1186/s11658-022-00359-z.

DOI:10.1186/s11658-022-00359-z
PMID:35842587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9287902/
Abstract

Recently, mesenchymal stromal cell (MSC)-based therapy has become an appreciated therapeutic approach in the context of neurodegenerative disease therapy. Accordingly, a myriad of studies in animal models and also some clinical trials have evinced the safety, feasibility, and efficacy of MSC transplantation in neurodegenerative conditions, most importantly in Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS), and Huntington's disease (HD). The MSC-mediated desired effect is mainly a result of secretion of immunomodulatory factors in association with release of various neurotrophic factors (NTFs), such as glial cell line-derived neurotrophic factor (GDNF) and brain-derived neurotrophic factor (BDNF). Thanks to the secretion of protein-degrading molecules, MSC therapy mainly brings about the degradation of pathogenic protein aggregates, which is a typical appearance of chronic neurodegenerative disease. Such molecules, in turn, diminish neuroinflammation and simultaneously enable neuroprotection, thereby alleviating disease pathological symptoms and leading to cognitive and functional recovery. Also, MSC differentiation into neural-like cells in vivo has partially been evidenced. Herein, we focus on the therapeutic merits of MSCs and also their derivative exosome as an innovative cell-free approach in AD, HD, PD, and ALS conditions. Also, we give a brief glimpse into novel approaches to potentiate MSC-induced therapeutic merits in such disorders, most importantly, administration of preconditioned MSCs.

摘要

最近,间充质基质细胞(MSC)治疗在神经退行性疾病治疗中已成为一种备受关注的治疗方法。因此,在动物模型中的大量研究以及一些临床试验已经证明了 MSC 移植在神经退行性疾病中的安全性、可行性和有效性,尤其是在阿尔茨海默病(AD)、帕金森病(PD)、肌萎缩侧索硬化症(ALS)和亨廷顿病(HD)中。MSC 介导的所需效果主要是由于免疫调节因子的分泌与各种神经营养因子(NTFs)的释放有关,例如胶质细胞系衍生的神经营养因子(GDNF)和脑源性神经营养因子(BDNF)。由于分泌蛋白降解分子,MSC 治疗主要导致致病蛋白聚集体的降解,这是慢性神经退行性疾病的典型表现。这些分子反过来又减轻神经炎症,同时实现神经保护,从而缓解疾病的病理症状并导致认知和功能恢复。此外,MSC 在体内分化为类神经细胞的现象也得到了部分证实。在此,我们重点介绍 MSC 及其衍生的外泌体在 AD、HD、PD 和 ALS 中的治疗优势,这是一种创新的无细胞方法。此外,我们简要介绍了在这些疾病中增强 MSC 诱导的治疗优势的新方法,尤其是预处理 MSC 的给药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/3b7be27e5f7a/11658_2022_359_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/b3f035ae3922/11658_2022_359_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/3142af93a574/11658_2022_359_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/3b7be27e5f7a/11658_2022_359_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/b3f035ae3922/11658_2022_359_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/3142af93a574/11658_2022_359_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d04e/9287902/3b7be27e5f7a/11658_2022_359_Fig3_HTML.jpg

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