首页> 美国卫生研究院文献>Frontiers in Neurology >Early Microglial Activation Following Closed-Head Concussive Injury Is Dominated by Pro-Inflammatory M-1 Type
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Early Microglial Activation Following Closed-Head Concussive Injury Is Dominated by Pro-Inflammatory M-1 Type

机译:闭合性脑震荡损伤后的早期小胶质细胞活化主要由促炎性M-1型决定。

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摘要

Microglial activation is a pathological hallmark of traumatic brain injury (TBI). Following brain injury, activated microglia/macrophages adopt different phenotypes, generally categorized as M-1, or classically activated, and M-2, or alternatively activated. While the M-1, or pro-inflammatory phenotype is detrimental to recovery, M-2, or the anti-inflammatory phenotype, aids in brain repair. Recent findings also suggest the existence of mixed phenotype following brain injury, where activated microglia simultaneously express both M-1 and M-2 markers. The present study sought to determine microglial activation states at early time points (6–72 h) following single or repeated concussive injury in rats. Closed-head concussive injury was modeled in rats using projectile concussive impact injury, with either single or repeated impacts (4 impacts, 1 h apart). Brain samples were examined using immunohistochemical staining, inflammatory gene profiling and real-time polymerase chain reaction analyses to detect concussive injury induced changes in microglial activation and phenotype in cortex and hippocampal regions. Our findings demonstrate robust microglial activation following concussive brain injury. Moreover, we show that multiple concussions induced a unique rod-shaped microglial morphology that was also observed in other diffuse brain injury models. Histological studies revealed a predominance of MHC-II positive M-1 phenotype in the post-concussive microglial milieu following multiple impacts. Although there was simultaneous expression of M-1 and M-2 markers, gene expression results indicate a clear dominance in M-1 pro-inflammatory markers following both single and repeated concussions. While the increase in M-1 markers quickly resolved after a single concussion, they persisted following repeated concussions, indicating a pro-inflammatory environment induced by multiple concussions that may delay recovery and contribute to long-lasting consequences of concussion.
机译:小胶质细胞激活是脑外伤(TBI)的病理标志。脑损伤后,活化的小胶质细胞/巨噬细胞采用不同的表型,通常归类为M-1(或经典活化)和M-2(或另选为活化)。 M-1或促炎表型不利于恢复,而M-2或消炎表型有助于脑部修复。最近的发现还表明脑损伤后存在混合表型,其中活化的小胶质细胞同时表达M-1和M-2标记。本研究试图确定大鼠单次或反复脑震荡损伤后早期时间点(6-72小时)的小胶质细胞活化状态。在大鼠中,使用抛射性脑震荡冲击伤害对闭合性脑震荡伤害进行建模,该冲击具有单次或重复冲击(4次冲击,相隔1小时)。使用免疫组织化学染色,炎性基因分析和实时聚合酶链反应分析检查脑样本,以检测脑震荡引起的皮层和海马区小胶质细胞活化和表型变化。我们的发现表明脑震荡后小胶质细胞活化活跃。此外,我们显示多个脑震荡诱发了独特的杆状小胶质细胞形态,在其他弥漫性脑损伤模型中也观察到了。组织学研究表明,脑震荡后小胶质细胞环境中受到多种影响后,MHC-II阳性M-1表型占主导地位。尽管同时表达了M-1和M-2标记,但基因表达结果表明,在一次和两次脑震荡后,M-1促炎标记均具有明显优势。尽管一次脑震荡后M-1标记物的增加迅速消失,但在反复脑震荡后它们仍持续存在,这表明由多个脑震荡诱发的促炎环境可能会延迟恢复并导致脑震荡的长期后果。

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