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Progress of mesenchymal stem cell therapy for neural and retinal diseases

机译:间充质干细胞治疗神经和视网膜疾病的研究进展

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摘要

Complex circuitry and limited regenerative power make central nervous system (CNS) disorders the most challenging and difficult for functional repair. With elusive disease mechanisms, traditional surgical and medical interventions merely slow down the progression of the neurodegenerative diseases. However, the number of neurons still diminishes in many patients. Recently, stem cell therapy has been proposed as a viable option. Mesenchymal stem cells (MSCs), a widely-studied human adult stem cell population, have been discovered for more than 20 years. MSCs have been found all over the body and can be conveniently obtained from different accessible tissues: bone marrow, blood, and adipose and dental tissue. MSCs have high proliferative and differentiation abilities, providing an inexhaustible source of neurons and glia for cell replacement therapy. Moreover, MSCs also show neuroprotective effects without any genetic modification or reprogramming. In addition, the extraordinary immunomodulatory properties of MSCs enable autologous and heterologous transplantation. These qualities heighten the clinical applicability of MSCs when dealing with the pathologies of CNS disorders. Here, we summarize the latest progress of MSC experimental research as well as human clinical trials for neural and retinal diseases. This review article will focus on multiple sclerosis, spinal cord injury, autism, glaucoma, retinitis pigmentosa and age-related macular degeneration.
机译:复杂的电路和有限的再生能力使中枢神经系统(CNS)疾病成为功能修复中最具挑战性和最困难的疾病。由于疾病机制难以捉摸,传统的外科和医学干预措施只能减缓神经退行性疾病的发展。但是,许多患者的神经元数量仍在减少。最近,已经提出干细胞疗法作为可行的选择。间充质干细胞(MSCs)是一种经过广泛研究的人类成年干细胞群体,现已发现20多年了。 MSC已遍布全身,可以方便地从各种可及的组织中获得:骨髓,血液,脂肪和牙齿组织。 MSC具有高增殖和分化能力,为细胞替代治疗提供了神经和胶质细胞的不竭来源。此外,MSC还显示出神经保护作用,而没有任何基因修饰或重新编程。此外,MSC的非凡免疫调节特性使自体和异体移植成为可能。这些质量在处理中枢神经系统疾病的病理过程中提高了MSC的临床适用性。在这里,我们总结了MSC实验研究的最新进展以及神经和视网膜疾病的人体临床试验。本文将重点讨论多发性硬化症,脊髓损伤,自闭症,青光眼,色素性视网膜炎和年龄相关性黄斑变性。

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