Role of Oligodendrocyte Lineage Cells in White Matter Injury.

Q3 Neuroscience
Katarzyna Pieczonka, Oliver Zhang, Sogolie Kouhzaei, Alexander A Velumian, Michael G Fehlings
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引用次数: 0

Abstract

This chapter provides a comprehensive review of white matter injuries, with a particular focus on oligodendrocyte lineage cell-mediated mechanisms and strategies. Traumatic mechanical insults, vascular conditions, perinatal injuries, and degenerative diseases all have white matter components and can be studied using different animal models. These distinct etiologies converge on similar pathophysiological features comprised of programmed cell death of oligodendrocyte lineage cells, demyelination, release of myelin debris, ion imbalance, excitotoxicity, mitochondrial dysfunction, and Wallerian degeneration. Therapeutics that target oligodendrocyte lineage cells are warranted due to their role in remyelination, immunomodulation, circuit remodeling, and maintenance of vasculature. Thus, emerging diagnostic techniques can help in assessing the extent of oligodendrocyte lineage cell-related pathology, while regenerative treatments, including cell transplantation, endogenous cell mobilization, biomaterials, and rehabilitation, can facilitate recovery by driving regeneration of oligodendrocyte lineage cells and myelin. Despite tremendous progress in this field, the heterogeneity of oligodendrocyte lineage cells suggests that a personalized medicine approach may optimize recovery following injury.

少突胶质细胞系细胞在白质损伤中的作用。
本章提供了一个全面的审查白质损伤,特别侧重于少突胶质细胞谱系细胞介导的机制和策略。创伤性机械损伤、血管状况、围产期损伤和退行性疾病都有白质成分,可以使用不同的动物模型进行研究。这些不同的病因集中在相似的病理生理特征上,包括少突胶质细胞系细胞的程序性细胞死亡、脱髓鞘、髓磷脂碎片的释放、离子失衡、兴奋毒性、线粒体功能障碍和沃勒氏变性。由于少突胶质细胞在髓鞘再生、免疫调节、电路重塑和血管系统维持中的作用,靶向治疗是必要的。因此,新兴的诊断技术可以帮助评估少突胶质细胞谱系细胞相关病理的程度,而再生治疗,包括细胞移植、内源性细胞动员、生物材料和康复,可以通过驱动少突胶质细胞谱系细胞和髓磷脂的再生来促进恢复。尽管在这一领域取得了巨大的进展,但少突胶质细胞谱系细胞的异质性表明,个性化的治疗方法可能会优化损伤后的恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
自引率
0.00%
发文量
0
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