小胶质细胞
神经炎症
炎症
神经保护
巨噬细胞
巨噬细胞极化
医学
神经科学
脊髓损伤
再生(生物学)
免疫学
细胞生物学
生物
脊髓
体外
生物化学
作者
Sheng-Ping Fu,Siyu Chen,Qi-Ming Pang,Meng Zhang,Xiang-Chong Wu,Xue Wan,Wenbin Wan,Jun Ao,Tao Zhang
标识
DOI:10.3389/fimmu.2022.1014013
摘要
It is often difficult to regain neurological function following spinal cord injury (SCI). Neuroinflammation is thought to be responsible for this failure. Regulating the inflammatory response post-SCI may contribute to the recovery of neurological function. Over the past few decades, studies have found that macrophages/microglia are one of the primary effector cells in the inflammatory response following SCI. Growing evidence has documented that macrophages/microglia are plastic cells that can polarize in response to microenvironmental signals into M1 and M2 macrophages/microglia. M1 produces pro-inflammatory cytokines to induce inflammation and worsen tissue damage, while M2 has anti-inflammatory activities in wound healing and tissue regeneration. Recent studies have indicated that the transition from the M1 to the M2 phenotype of macrophage/microglia supports the regression of inflammation and tissue repair. Here, we will review the role of the inflammatory response and macrophages/microglia in SCI and repair. In addition, we will discuss potential molecular mechanisms that induce macrophage/microglia polarization, with emphasis on neuroprotective therapies that modulate macrophage/microglia polarization, which will provide new insights into therapeutic strategies for SCI.
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