Xia Yiming, Cai Min, Zhou Yiyue, Yao Yi, Jiang Maorong, Gu Dandan, Yao Dengbing
Medical School of Nantong University, Nantong, Jiangsu, P.R. China.
School of Life Sciences, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu, P.R. China.
Neurorehabil Neural Repair. 2025 Mar;39(3):230-240. doi: 10.1177/15459683241304325. Epub 2025 Jan 2.
The peripheral nervous system (PNS) exhibits remarkable regenerative capability after injury. PNS regeneration relies on neurons themselves as well as a variety of other cell types, including Schwann cells, immune cells, and non-neuronal cells.
This paper focuses on summarizing the critical roles of immune cells (SCs) in the injury and repair processes of the PNS.
During peripheral nerve injury, macrophages infiltrate the site under the induction of various cytokines, primarily accumulating at the dorsal root ganglia (DRG) and the nerve distal to the injury site, with only a small number detected at the nerve proximal to the injury site. The phenotype of macrophages during injury remains controversial, but recent single-cell sequencing analyses may provide new insights. In peripheral nervous system injury, macrophages participate in Wallerian degeneration as well as in the reconstruction of nerve bridges and angiogenesis during axonal regeneration. Neutrophils appear early in the injury process and are primarily present at the injury site and the distal segment. After peripheral nervous system injury, immature neutrophils from the peripheral blood play a major role. Although lymphocytes constitute only a small fraction compared to macrophages and neutrophils after peripheral nervous system injury, they still play important roles, including Treg cells, B cells, and NK cells. A large number of immune cells accumulate at the injury site, contributing not only to Wallerian degeneration but also to axonal regeneration.
In conclusion, this paper summarizes current knowledge regarding the mechanisms of immune cell infiltration after PNS injury, providing new insights for future research on the role of immune cells in peripheral nerve injury.
周围神经系统(PNS)在损伤后具有显著的再生能力。PNS的再生依赖于神经元自身以及多种其他细胞类型,包括施万细胞、免疫细胞和非神经元细胞。
本文着重总结免疫细胞在PNS损伤和修复过程中的关键作用。
在周围神经损伤期间,巨噬细胞在各种细胞因子的诱导下浸润损伤部位,主要聚集在背根神经节(DRG)和损伤部位远端的神经处,而在损伤部位近端的神经处仅检测到少量巨噬细胞。损伤期间巨噬细胞的表型仍存在争议,但最近的单细胞测序分析可能会提供新的见解。在周围神经系统损伤中,巨噬细胞参与沃勒变性以及轴突再生过程中的神经桥重建和血管生成。中性粒细胞在损伤过程中早期出现,主要存在于损伤部位和远端节段。周围神经系统损伤后,外周血中的未成熟中性粒细胞起主要作用。尽管与巨噬细胞和中性粒细胞相比,淋巴细胞在周围神经系统损伤后仅占一小部分,但它们仍发挥重要作用,包括调节性T细胞、B细胞和自然杀伤细胞。大量免疫细胞在损伤部位积聚,不仅促进沃勒变性,还促进轴突再生。
总之,本文总结了关于PNS损伤后免疫细胞浸润机制的现有知识,为未来研究免疫细胞在周围神经损伤中的作用提供了新的见解。