横断损伤后坐骨神经单细胞转录组图。

IF 10.1 1区 医学 Q1 IMMUNOLOGY
Yiben Ouyang, Mingqian Yu, Tieyuan Zhang, Haofeng Cheng, Liang Zuo, Haolin Liu, Yanjun Guan, Ao Liu, Jiajie Chen, Ruichao He, Sice Wang, Tianqi Su, Yixiao Tan, Yuhui Cu, Xiaochun Zhang, Xiaoyang Fu, Junli Wang, Jinjuan Zhao, Jiang Peng, Yu Wang
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引用次数: 0

摘要

周围神经损伤,特别是影响坐骨神经的损伤,由于成人周围神经的再生能力有限,往往导致功能恢复不完全。为了阐明神经再生的细胞和分子机制,我们在横断损伤后的7个时间点(0、1、3、5、7、10和14天)对大鼠坐骨神经组织进行了单细胞RNA测序(scRNA-seq)。通过无监督聚类,我们确定了四种主要的细胞区室——神经成纤维细胞(NFs)、神经胶质细胞(Glis)、免疫细胞和血管细胞,并描绘了它们在再生过程中的动态轨迹。早期反应主要是巨噬细胞(Mac)和粒细胞浸润(第1天),随后是增殖间充质成纤维细胞(NF5)的增殖扩张和修复雪旺细胞(Gli0)。血管重构从第7天开始,到第14天,胶质细胞逐渐过渡到成熟的髓鞘状态(Gli2/Gli5)。伪时间分析揭示了mac和Glis中亚型特异性重编程,细胞-细胞通讯分析揭示了关键的配体-受体相互作用,特别是mac、NFs和Glis之间的胶原蛋白和PTN信号。大量转录组学验证证实了TGF-信号通路在不同细胞类型和解剖位置的持续和空间上的不同激活。与坐骨神经挤压损伤模型的比较分析显示,横断损伤的早期免疫反应更强,Gli恢复延迟,表明治疗窗口缩小。总之,这项工作提供了一个时间分辨的周围神经再生单细胞图谱,定义了免疫- nf - gli轴内的关键调控回路,并确定了阶段特异性治疗靶点,如早期Mac异质性,nf4介导的基质重塑和雪旺细胞髓鞘再生,以增强严重神经损伤后的功能恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single-cell transcriptomic landscape of sciatic nerve after transection injury.

Peripheral nerve injuries, particularly those affecting the sciatic nerve, often result in incomplete functional recovery due to the limited regenerative capacity of adult peripheral nerves. To elucidate the cellular and molecular mechanisms underlying nerve regeneration, we performed single-cell RNA sequencing (scRNA-seq) on rat sciatic nerve tissues at seven time points (Days 0, 1, 3, 5, 7, 10, and 14) following transection injury. Through unsupervised clustering, we identified four major cellular compartments-neurofibroblasts (NFs), glial cells (Glis), immune cells, and vascular cells-and delineated their dynamic trajectories during regeneration. Early responses were dominated by macrophage (Mac) and granulocyte infiltration (Day 1), followed by proliferative expansion of proliferating mesenchymal fibroblasts (NF5) and repair Schwann cells (Gli0) by Days 3-5. Vascular remodeling commenced from Day 7, while Glis progressively transitioned to mature myelinating states (Gli2/Gli5) by Day 14. Pseudotime analysis revealed subtype-specific reprogramming in both Macs and Glis, and cell-cell communication analysis uncovered key ligand-receptor interactions-particularly collagen and PTN signaling between Macs, NFs, and Glis. Bulk transcriptomic validation confirmed sustained and spatially distinct activation of the TGF-[Formula: see text] signaling pathway across cell types and anatomical locations. Comparative analysis with a sciatic nerve crush injury model revealed a stronger early immune response and delayed Gli recovery in transection injury, indicating a narrowed therapeutic window. Together, this work provides a time-resolved single-cell atlas of peripheral nerve regeneration, defines key regulatory circuits within the immune-NF-Gli axis, and identifies phase-specific therapeutic targets-such as early Mac heterogeneity, NF4-mediated matrix remodeling, and Schwann cell remyelination-for enhancing functional recovery following severe nerve injury.

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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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