Lin T N, Wang P Y, Chi S I, Kuo J S
Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Brain Res Mol Brain Res. 1998 Mar 30;55(1):71-80. doi: 10.1016/s0169-328x(97)00367-7.
Ciliary neurotrophic factor (CNTF) is a member of cytokines, with trophic effects on ciliary, motor sympathetic, sensory, retinal and hippocampal neurons. In the present study, we examined the temporal and spatial expression profiles of CNTF and CNTF receptor alpha (CNTFR alpha) mRNAs in a focal cerebral ischemia model induced by transient occlusion of the right middle cerebral artery and both common carotid arteries. Northern blot analysis showed a slow and sustained increase in the 1.2 kb transcript of CNTF mRNA in the ischemic cortex of rats subjected to a transient 60 min ischemic insult. A delayed decrease in the 2.1 kb transcript of CNTFR alpha mRNA in the ischemic cortex was observed in rats subjected to 60 min ischemia followed by 72 h of reperfusion. In situ hybridization studies revealed constitutive expression of CNTFR alpha mRNA in the majority of neurons in the brain. Following 4 h of reperfusion, increased expression of CNTFR alpha mRNA was observed in the ipsilateral dentate gyrus, which is opposite to the down-regulation noted in the ischemic cortex. Within the infarct area CNTFR alpha mRNA had a marked increase in cortical layer II but a decrease in cortical layer V following 1 day of reperfusion. No signal of CNTFR alpha mRNA was detected within the infarct region following 3 days of reperfusion. Following 1 week of reperfusion, although no marked changes was observed in the level of CNTFR alpha mRNA in the area immediately surrounding the necrosis region where the reactive astrocytes were noted, a striking increase in the CNTF mRNA signal was noted. In summary, differential regulation of CNTF and CNTFR alpha mRNAs was noted in the ischemic cortex. Regional differences in CNTF receptor expression were noted between the ischemic cortex and ipsilateral dentate gyrus as well as between cortical layer II and V within the infarct region. CNTF mRNA, but not CNTFR alpha mRNA, had a marked increase in the area immediately adjacent to the necrosis. The mechanisms and patho-physiological significance for these differential regulation remain to be studied.
睫状神经营养因子(CNTF)是细胞因子的一员,对睫状、运动交感、感觉、视网膜和海马神经元具有营养作用。在本研究中,我们检测了在右侧大脑中动脉和双侧颈总动脉短暂闭塞诱导的局灶性脑缺血模型中CNTF和CNTF受体α(CNTFRα)mRNA的时空表达谱。Northern印迹分析显示,在经历短暂60分钟缺血损伤的大鼠缺血皮质中,CNTF mRNA的1.2 kb转录本缓慢且持续增加。在经历60分钟缺血后再灌注72小时的大鼠中,观察到缺血皮质中CNTFRα mRNA的2.1 kb转录本延迟下降。原位杂交研究显示,CNTFRα mRNA在大脑中的大多数神经元中组成性表达。再灌注4小时后,在同侧齿状回中观察到CNTFRα mRNA表达增加,这与缺血皮质中观察到的下调相反。再灌注1天后,梗死区域内CNTFRα mRNA在皮质层II中显著增加,但在皮质层V中减少。再灌注3天后,在梗死区域内未检测到CNTFRα mRNA信号。再灌注1周后,尽管在紧邻有反应性星形胶质细胞的坏死区域周围区域中,CNTFRα mRNA水平未观察到明显变化,但CNTF mRNA信号显著增加。总之,在缺血皮质中观察到CNTF和CNTFRα mRNA的差异调节。在缺血皮质和同侧齿状回之间以及梗死区域内的皮质层II和V之间,注意到CNTF受体表达的区域差异。在紧邻坏死区域的区域中,CNTF mRNA而非CNTFRα mRNA显著增加。这些差异调节的机制和病理生理意义仍有待研究。