再髓鞘化
髓鞘
吞噬作用
小胶质细胞
巨噬细胞
脊髓
脊髓损伤
再生(生物学)
细胞生物学
生物
神经科学
炎症
细胞内
免疫学
中枢神经系统
体外
生物化学
作者
Jana Van Broeckhoven,Daniela Sommer,Dearbhaile Dooley,Sven Hendrix,Aimée J. P. M. Franssen
出处
期刊:Brain
[Oxford University Press]
日期:2021-07-07
卷期号:144 (10): 2933-2945
被引量:83
标识
DOI:10.1093/brain/awab250
摘要
After spinal cord injury, macrophages can exert either beneficial or detrimental effects depending on their phenotype. Aside from their critical role in inflammatory responses, macrophages are also specialized in the recognition, engulfment, and degradation of pathogens, apoptotic cells, and tissue debris. They promote remyelination and axonal regeneration by removing inhibitory myelin components and cellular debris. However, excessive intracellular presence of lipids and dysregulated intracellular lipid homeostasis result in the formation of foamy macrophages. These develop a pro-inflammatory phenotype that may contribute to further neurological decline. Additionally, myelin-activated macrophages play a crucial role in axonal dieback and retraction. Here, we review the opposing functional consequences of phagocytosis by macrophages in spinal cord injury, including remyelination and regeneration versus demyelination, degeneration, and axonal dieback. Furthermore, we discuss how targeting the phagocytic ability of macrophages may have therapeutic potential for the treatment of spinal cord injury.
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