Transplantation of human glial cells into murine brains: A systematic review of efficacy and safety in neurodegenerative disorders.

IF 0.9 Q4 CLINICAL NEUROLOGY
Sanjeev Kumar Jain, Sonika Sharma, Vinod Kumar Singh, Prithpal Singh Matreja
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引用次数: 0

Abstract

Background: Neurodegenerative diseases impact millions of individuals globally. Over the years, brain research has predominantly focused on neurons, but attention is now shifting to glial cells, the brain's support cells, which play a vital role in neurodegenerative disorders. Therefore, glial cell transplantation represents a groundbreaking treatment approach for various neurodegenerative disorders, with the potential to restore neuronal function. We evaluated the evidence on the therapeutic effectiveness of human glial cell transplantation in neurodegenerative disorders. Methods: The literature review was performed in PubMed, Scopus, and Web of Science from 2000 to 2024. The authors independently reviewed the screened articles. The study outcomes on cell differentiation, long survival restoration of neuron function, and adverse outcomes were analyzed. Results: Study results highlight promising findings, including astrocytes improving motor function and slowing disease progression in neurodegenerative animal models through neurotrophic factor secretion and reduced inflammation. Similarly, microglia transplantation has demonstrated effectiveness in reducing α-synuclein toxicity in Parkinson's disease (PD), removing amyloid-β plaques in Alzheimer's disease (AD) models, and enhancing neuronal survival. Additionally, in demyelinating pathologies like multiple sclerosis (MS), oligodendrocyte transplantation promotes remyelination, restoring axonal conduction and enhancing functional outcomes. Cografting astrocytes with neuro progenitor cells significantly improved dopamine neuron engraftment and survival for at least 6 months post-transplantation. Conclusion: The transplantation of human glial cells offers promising therapeutic potential for neurodegenerative disorders, improving neuronal survival, restoring damaged circuits, and reducing disease progression.

人类神经胶质细胞移植到小鼠大脑:对神经退行性疾病的有效性和安全性的系统评价。
背景:神经退行性疾病影响着全球数百万人。多年来,大脑研究主要集中在神经元上,但现在注意力转向神经胶质细胞,这是大脑的支持细胞,在神经退行性疾病中起着至关重要的作用。因此,神经胶质细胞移植代表了一种突破性的治疗各种神经退行性疾病的方法,具有恢复神经元功能的潜力。我们评估了人类神经胶质细胞移植治疗神经退行性疾病的有效性。方法:检索2000 ~ 2024年PubMed、Scopus、Web of Science的相关文献。作者独立审查筛选的文章。分析了细胞分化、神经元功能长期存活恢复及不良反应的研究结果。结果:研究结果突出了有希望的发现,包括星形胶质细胞通过神经营养因子分泌和减少炎症来改善神经退行性动物模型的运动功能和减缓疾病进展。同样,小胶质细胞移植在帕金森病(PD)中的α-突触核蛋白毒性降低,在阿尔茨海默病(AD)模型中去除淀粉样蛋白-β斑块,以及提高神经元存活率方面也已被证明有效。此外,在多发性硬化症(MS)等脱髓鞘病变中,少突胶质细胞移植可促进髓鞘再生,恢复轴突传导并增强功能结果。星形胶质细胞与神经祖细胞共移植可显著改善多巴胺神经元的植入和移植后至少6个月的存活率。结论:人神经胶质细胞移植在治疗神经退行性疾病、改善神经元存活、修复受损神经回路和减缓疾病进展方面具有广阔的应用前景。
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来源期刊
Current Journal of Neurology
Current Journal of Neurology CLINICAL NEUROLOGY-
CiteScore
0.80
自引率
14.30%
发文量
30
审稿时长
12 weeks
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