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Expression changes of CX3CL1 and CX3CR1 proteins in the hippocampal CA1 field of the gerbil following transient global cerebral ischemia

机译:短暂性全脑缺血后沙土鼠海马CA1区CX3CL1和CX3CR1蛋白的表达变化

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摘要

Chemokine C-X3-C motif ligand 1 (CX3CL1) and its sole receptor, CX3CR1, are known to be involved in neuronal damage/death following brain ischemia. In the present study, time-dependent expression changes of CX3CL1 and CX3CR1 proteins were investigated in the hippocampal CA1 field following 5 min of transient global cerebral ischemia (tgCI) in gerbils. To induce tgCI in gerbils, bilateral common carotid arteries were occluded for 5 min using aneurysm clips. Expression changes of CX3CL1 and CX3CR1 proteins were assessed at 1, 2 and 5 days after tgCI using western blotting and immunohistochemistry. CX3CL1 immunoreactivity was strong in the CA1 pyramidal cells of animals in the sham operation group. Weak CX3CL1 immunoreactivity was detected at 6 h after tgCI, recovered at 1 day after tgCI and disappeared from 5 days after tgCI. CX3CR1 immunoreactivity was very weak in CA1 pyramidal cells of the sham animals. CX3CR1 immunoreactivity in CA1 pyramidal cells was significantly increased at 1 days after tgCI and gradually decreased thereafter. On the other hand, CX3CR1 immunoreactivity was significantly increased in microglia from 5 days after tgCI. These results showed that CX3CL1 and CX3CR1 protein expression levels in pyramidal cells and microglia in the hippocampal CA1 field following tgCI were changed, indicating that tgCI-induced expression changes of CX3CL1 and CX3CR1 proteins might be closely associated with tgCI-induced delayed neuronal death and microglial activation.
机译:已知趋化因子C-X3-C基序配体1(CX3CL1)及其唯一受体CX3CR1参与脑缺血后的神经元损害/死亡。在本研究中,研究了沙土鼠短暂性全脑缺血(tgCI)5分钟后海马CA1场中CX3CL1和CX3CR1蛋白的时间依赖性表达变化。为了在沙鼠中诱导tgCI,使用动脉瘤夹将双侧颈总动脉闭塞5分钟。使用蛋白质印迹和免疫组织化学方法,在tgCI后第1、2和5天评估CX3CL1和CX3CR1蛋白的表达变化。假手术组动物的CA1锥体细胞中CX3CL1的免疫反应性强。在tgCI后6小时检测到弱的CX3CL1免疫反应性,在tgCI后1天恢复,并在tgCI后5天消失。在假动物的CA1锥体细胞中,CX3CR1免疫反应性非常弱。在tgCI后1天,CA1锥体细胞中的CX3CR1免疫反应性显着增加,此后逐渐降低。另一方面,从tgCI后5天开始,小胶质细胞中的CX3CR1免疫反应性显着增加。这些结果表明,tgCI后海马CA1区锥体细胞和小胶质细胞中CX3CL1和CX3CR1蛋白的表达水平发生了改变,表明tgCI诱导的CX3CL1和CX3CR1蛋白的表达变化可能与tgCI诱导的迟发性神经元死亡和小胶质细胞紧密相关激活。

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