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骨髓来源的单核细胞驱动胸段脊髓损伤后局部和远处区域的炎症微环境。

Bone Marrow-Derived Monocytes Drive the Inflammatory Microenvironment in Local and Remote Regions after Thoracic Spinal Cord Injury.

机构信息

1 School of Health and Rehabilitation Sciences, The Ohio State University, Columbus, Ohio.

2 Center for Brain and Spinal Cord Repair, The Ohio State University, Columbus, Ohio.

出版信息

J Neurotrauma. 2019 Mar 19;36(6):937-949. doi: 10.1089/neu.2018.5806. Epub 2018 Oct 6.

Abstract

Spinal cord injury (SCI) produces a toxic inflammatory microenvironment that negatively affects plasticity and recovery. Recently, we showed glial activation and peripheral myeloid cell infiltration extending beyond the epicenter through the remote lumbar cord after thoracic SCI. The presence and role of infiltrating monocytes is important, especially in the lumbar cord where locomotor central pattern generators are housed. Therefore, we compared the inflammatory profile of resident microglia and peripheral myeloid cells after SCI. Bone marrow chimeras received midthoracic contusive SCI, and trafficking was determined 1-7 days later. Fluorescence-activated cell (FAC) sorting showed similar infiltration timing of both neutrophils and macrophages in epicenter and lumbar regions. While neutrophil numbers were attenuated by day 3, macrophages remained unchanged at day 7, suggesting that macrophages have important long-term influence on the microenvironment. Nanostring gene array identified a strong proinflammatory profile of infiltrating macrophages relative to microglia at both epicenter and lumbar sites. Macrophages had elevated expression of inflammatory cytokines (IL-1β, IFNγ), chemokines (CCL2, CXCL2), mediators (COX-1, MMP-9), and receptors (CCR2, Ly6C), and decreased expression of growth promoting genes (GDNF, BDNF). Importantly, lumbar macrophages had elevated expression of active trafficking genes (CCR2, l-selectin, MMP-9) compared with epicenter macrophages. Further, acute rehabilitation exacerbated the inflammatory profile of infiltrated macrophages in the lumbar cord. Such high inflammatory potential and negative response to rehabilitation of infiltrating macrophages within lumbar locomotor central pattern generators likely impedes activity-dependent recovery. Therefore, limiting active trafficking of macrophages into the lumbar cord identifies a novel target for SCI therapies to improve locomotion.

摘要

脊髓损伤 (SCI) 会产生有毒的炎症微环境,对可塑性和恢复产生负面影响。最近,我们发现,在胸 SCI 后,胶质细胞的激活和外周髓样细胞的浸润会穿过远程腰椎脊髓而超出损伤中心。浸润单核细胞的存在和作用很重要,尤其是在容纳运动中枢模式发生器的腰椎脊髓中。因此,我们比较了 SCI 后驻留小胶质细胞和外周髓样细胞的炎症特征。骨髓嵌合体接受胸段压迫性 SCI,然后在 1-7 天后确定迁移情况。荧光激活细胞 (FAC) 分选显示,在损伤中心和腰椎区域,中性粒细胞和巨噬细胞的浸润时间相似。尽管中性粒细胞数量在第 3 天减少,但巨噬细胞在第 7 天没有变化,这表明巨噬细胞对微环境有重要的长期影响。纳米字符串基因阵列鉴定出,与损伤中心和腰椎部位的小胶质细胞相比,浸润巨噬细胞具有强烈的促炎特征。巨噬细胞表达的炎症细胞因子(IL-1β、IFNγ)、趋化因子(CCL2、CXCL2)、介质(COX-1、MMP-9)和受体(CCR2、Ly6C)增加,促进生长的基因(GDNF、BDNF)表达减少。重要的是,与损伤中心的巨噬细胞相比,腰椎巨噬细胞表达的主动迁移基因(CCR2、l-选择素、MMP-9)更高。此外,急性康复加剧了腰椎脊髓中浸润巨噬细胞的炎症特征。在腰椎运动中枢模式发生器中,浸润巨噬细胞具有如此高的炎症潜力和对康复的负面反应,可能会阻碍与活动相关的恢复。因此,限制巨噬细胞主动迁移到腰椎脊髓为 SCI 治疗改善运动功能提供了一个新的靶点。

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