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揭示神经干细胞/祖细胞在多发性硬化症中的命运及潜在神经保护作用。

Unveiling the fate and potential neuroprotective role of neural stem/progenitor cells in multiple sclerosis.

作者信息

Hijal Nora, Fouani Malak, Awada Bassel

机构信息

Department of Nursing, American University of Beirut Medical Center, Beirut, Lebanon.

Department of Neurology, Duke University Medical Center, Durham, NC, United States.

出版信息

Front Neurol. 2024 Nov 20;15:1438404. doi: 10.3389/fneur.2024.1438404. eCollection 2024.

Abstract

Chronic pathological conditions often induce persistent systemic inflammation, contributing to neuroinflammatory diseases like Multiple Sclerosis (MS). MS is known for its autoimmune-mediated damage to myelin, axonal injury, and neuronal loss which drive disability accumulation and disease progression, often manifesting as cognitive impairments. Understanding the involvement of neural stem cells (NSCs) and neural progenitor cells (NPCs) in the remediation of MS through adult neurogenesis (ANG) and gliogenesis-the generation of new neurons and glial cells, respectively is of great importance. Hence, these phenomena, respectively, termed ANG and gliogenesis, involve significant structural and functional changes in neural networks. Thus, the proper integration of these newly generated cells into existing circuits is not only key to understanding the CNS's development but also its remodeling in adulthood and recovery from diseases such as MS. Understanding how MS influences the fate of NSCs/NPCs and their possible neuroprotective role, provides insights into potential therapeutic interventions to alleviate the impact of MS on cognitive function and disease progression. This review explores MS, its pathogenesis, clinical manifestations, and its association with ANG and gliogenesis. It highlights the impact of altered NSCs and NPCs' fate during MS and delves into the potential benefits of its modifications. It also evaluates treatment regimens that influence the fate of NSCS/NPCs to counteract the pathology subsequently.

摘要

慢性病理状况常常引发持续性全身炎症,进而导致诸如多发性硬化症(MS)等神经炎症性疾病。MS以其自身免疫介导的髓鞘损伤、轴突损伤和神经元丢失而闻名,这些损伤会导致残疾累积和疾病进展,常表现为认知障碍。了解神经干细胞(NSCs)和神经祖细胞(NPCs)通过成人神经发生(ANG)和胶质生成(分别指新神经元和神经胶质细胞的生成)参与MS修复的过程非常重要。因此,这些分别被称为ANG和胶质生成的现象,涉及神经网络中显著的结构和功能变化。因此,将这些新生成的细胞正确整合到现有神经回路中,不仅是理解中枢神经系统发育的关键,也是理解其成年期重塑以及从MS等疾病中恢复的关键。了解MS如何影响神经干细胞/神经祖细胞的命运及其可能的神经保护作用,有助于深入了解潜在的治疗干预措施,以减轻MS对认知功能和疾病进展的影响。本综述探讨了MS、其发病机制、临床表现及其与成人神经发生和胶质生成的关联。它强调了MS期间神经干细胞和神经祖细胞命运改变的影响,并深入探讨了其改变的潜在益处。它还评估了影响神经干细胞/神经祖细胞命运以对抗后续病理过程的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1707/11614735/c16acfdd1214/fneur-15-1438404-g001.jpg

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