Microglial response to early ischemia‐induced changes in the rat spinal cord

K. Saganová, J. Mars̆ala, T. Ondrejčák, I. Vanický, J. Gálik
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引用次数: 2

Abstract

We examined the early microglial response to spinal cord ischemia induced by occlusion of the descending aorta for 15 min, or more limited aortic occlusion (8, 10, 12 min( linked with blood volume reduction. The recovery of motor function and activation of microglia labeled by Griffonia simplicifolia B4-isolectin (GSA I-B4-HRP) were assessed up to 7 days post-ischemia. Activation of resident microglia characterized by both increased lectin binding and altered morphology was observed >48 hrs post-ischemia. Massive infiltration of the microglia/macrophages related to the severity of ischemic insult appeared at day 3. Our data suggest that (1) ischemia of different degrees gives rise to a generalized microglial response at the early post-ischemic phase; (2) graded activation of microglia/macrophases as a response to ischemic neuronal injury occurs within 48–72 hrs of post-ischemic reperfusion; (3) lectin labeling of microglia can serve for continuous study of the evolution of pathological changes associated with transient spinal cord ischemia.
小胶质细胞对早期缺血引起的大鼠脊髓变化的反应
我们检查了早期小胶质细胞对降主动脉阻断15分钟或更有限的主动脉阻断(8、10、12分钟)引起的脊髓缺血的反应(与血容量减少有关)。在缺血后7天,观察运动功能的恢复情况和单纯Griffonia B4-isolectin (GSA I-B4-HRP)标记的小胶质细胞活化情况。缺血后>48小时,观察到以凝集素结合增加和形态改变为特征的常驻小胶质细胞活化。第3天出现与缺血性损伤严重程度相关的小胶质细胞/巨噬细胞的大量浸润。我们的数据表明:(1)不同程度的缺血会在缺血后早期引起广泛的小胶质细胞反应;(2)在缺血再灌注后48-72小时内,小胶质细胞/大相对缺血性神经元损伤的反应发生分级激活;(3)对小胶质细胞进行凝集素标记,可为持续研究短暂性脊髓缺血相关病理变化的演变提供依据。
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