Gou Xingchun, Zhang Qiaomei, Xu Ning, Deng Bin, Wang Huiwen, Xu Lixian, Wang Qiang
Department of Anesthesiology, Stomatological College, Fourth Military Medical University , Xi'an , PR China .
Brain Inj. 2013;27(11):1311-5. doi: 10.3109/02699052.2013.812241. Epub 2013 Aug 8.
Paired immunoglobulin-like receptor-B (PirB) is another receptor, except for the Nogo receptor, that is involved in inhibition of axons regeneration after central nervous system injury. However, the expression of PirB in focal cerebral ischaemic brain remains unclear. Herein, this study investigated spatial-temporal expression of PirB in the mouse brain following transient focal cerebral ischaemia.
Adult male C57BL/6 mice underwent a 60-minute transient occlusion of middle cerebral artery. Mice were killed and brain samples were harvested at 30 minutes, 2 hours, 24 hours, 3 days and 7 days after reperfusion. Expression of PirB in the brain was determined by reverse transcriptase-polymerase chain reaction (RT-PCR), western blot analysis and immunohistochemical staining.
The results showed that PirB was mainly expressed in ischaemic penumbra. PirB mRNA and protein expression began to increase at 2 hours, peaked at 24 hours and lasted for 7 days after reperfusion in the ischaemic penumbra. By using immunofluorescence, PirB signals were co-localized with NeuN-positive neurons.
PirB expression is up-regulated in ischaemic penumbra following transient focal cerebral ischaemia. PirB expression in neurons may play important pathological roles in the inhibition of axonal regeneration after stroke, suggesting that the inhibition of PirB expression may enhance axonal regeneration and functional recovery after stroke.
除Nogo受体外,配对免疫球蛋白样受体B(PirB)是另一种参与中枢神经系统损伤后轴突再生抑制的受体。然而,PirB在局灶性脑缺血性脑中的表达仍不清楚。在此,本研究调查了短暂性局灶性脑缺血后小鼠脑中PirB的时空表达。
成年雄性C57BL/6小鼠接受大脑中动脉60分钟的短暂闭塞。在再灌注后30分钟、2小时、24小时、3天和7天处死小鼠并采集脑样本。通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹分析和免疫组织化学染色测定脑中PirB的表达。
结果显示,PirB主要在缺血半暗带表达。在缺血半暗带,PirB mRNA和蛋白表达在再灌注后2小时开始增加,24小时达到峰值,并持续7天。通过免疫荧光法,PirB信号与NeuN阳性神经元共定位。
短暂性局灶性脑缺血后缺血半暗带中PirB表达上调。神经元中PirB的表达可能在中风后轴突再生抑制中起重要病理作用,提示抑制PirB表达可能增强中风后轴突再生和功能恢复。