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首页> 外文期刊>Acta Neuropathologica >Very-late-antigen-4 (VLA-4)-mediated brain invasion by neutrophils leads to interactions with microglia, increased ischemic injury and impaired behavior in experimental stroke
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Very-late-antigen-4 (VLA-4)-mediated brain invasion by neutrophils leads to interactions with microglia, increased ischemic injury and impaired behavior in experimental stroke

机译:中性粒细胞介导的极晚期抗原4(VLA-4)介导的脑部入侵导致与小胶质细胞相互作用,缺血性损伤增加以及实验性中风行为受损

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Neuronal injury from ischemic stroke is aggravated by invading peripheral immune cells. Early infiltrates of neutrophil granulocytes and T-cells influence the outcome of stroke. So far, however, neither the timing nor the cellular dynamics of neutrophil entry, its consequences for the invaded brain area, or the relative importance of T-cells has been extensively studied in an intravital setting. Here, we have used intravital two-photon microscopy to document neutrophils and brain-resident microglia in mice after induction of experimental stroke. We demonstrated that neutrophils immediately rolled, firmly adhered, and transmigrated at sites of endothelial activation in stroke-affected brain areas. The ensuing neutrophil invasion was associated with local blood-brain barrier breakdown and infarct formation. Brain-resident microglia recognized both endothelial damage and neutrophil invasion. In a cooperative manner, they formed cytoplasmic processes to physically shield activated endothelia and trap infiltrating neutrophils. Interestingly, the systemic blockade of very-late-antigen-4 immediately and very effectively inhibited the endothelial interaction and brain entry of neutrophils. This treatment thereby strongly reduced the ischemic tissue injury and effectively protected the mice from stroke-associated behavioral impairment. Behavioral preservation was also equally well achieved with the antibody-mediated depletion of myeloid cells or specifically neutrophils. In contrast, T-cell depletion more effectively reduced the infarct volume without improving the behavioral performance. Thus, neutrophil invasion of the ischemic brain is rapid, massive, and a key mediator of functional impairment, while peripheral T-cells promote brain damage. Acutely depleting T-cells and inhibiting brain infiltration of neutrophils might, therefore, be a powerful early stroke treatment.
机译:周围性免疫细胞的入侵加剧了缺血性中风引起的神经元损伤。中性粒细胞和T细胞的早期浸润会影响中风的预后。然而,到目前为止,在活体环境中,尚未广泛研究嗜中性粒细胞进入的时间或细胞动力学,其对受侵袭的大脑区域的后果或T细胞的相对重要性。在这里,我们已经使用了活体两光子显微镜来记录实验性中风后小鼠中的中性粒细胞和脑部小胶质细胞。我们证明中性粒细胞在中风影响的大脑区域的内皮细胞活化位点立即滚动,牢固粘附并迁移。随后的中性粒细胞浸润与局部血脑屏障破坏和梗塞形成有关。驻留于大脑的小胶质细胞同时识别内皮损伤和中性粒细胞浸润。他们以协作的方式形成了细胞质过程,以物理屏蔽活化的内皮并捕获浸润的嗜中性粒细胞。有趣的是,非常晚期抗原4的全身性阻断立即且非常有效地抑制了嗜中性粒细胞的内皮相互作用和脑进入。因此,这种治疗极大地减少了缺血性组织损伤,并有效地保护了小鼠免受中风相关的行为损害。抗体介导的髓样细胞或中性粒细胞耗竭也同样可以很好地实现行为保存。相比之下,T细胞耗竭更有效地减少了梗塞体积而不改善行为表现。因此,中性粒细胞对缺血性脑的侵袭是快速,大量的,并且是功能障碍的关键介体,而外周T细胞会促进脑损伤。因此,急性消耗T细胞并抑制中性粒细胞脑浸润可能是一种有效的早期卒中治疗方法。

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