Wang Wei, Redecker Christoph, Bidmon Hans-Jürgen, Witte Otto W
Department of Neurology, Friedrich-Schiller University, Erlanger Allee 101, 07747 Jena, Germany.
Brain Res. 2004 Oct 8;1023(1):92-101. doi: 10.1016/j.brainres.2004.07.034.
Delayed neuronal death (DND) of pyramidal neurons in the CA1 and CA3 regions of the hippocampus has been extensively studied following global brain ischemia, whereas only little is known about DND in this highly vulnerable brain region after focal brain ischemia. In the present study, the distribution and time course of hippocampal neuronal apoptosis were studied following transient middle cerebral artery occlusion (MCAO) in rats 1, 3, 7, 14, and 30 days after the insult. In 60% of the animals, more than 90% of CA1 pyramidal neurons showed strong nick-end labeling (TUNEL) staining at day 3 with fragmentation and marginalization of the nuclei in approximately 40% of these cells. The number of TUNEL-positive cells decreased within the next days, but 30 days after MCAO, some apoptotic neurons were still present. Analysis of the expression of the glial cell line-derived neurotrophic factor (GDNF) and its receptors GFRalpha1, GFRalpha2, and GFRalpha3 using triple immunofluorescence and confocal laser scanning microscopy revealed that in all animals showing marked hippocampal DND, the neuronal staining for GFRalpha1, GFRalpha3, and GDNF decreased prior to the onset of TUNEL staining in CA1. After 7 days, some apoptotic neurons still expressed GFRalpha3, whereas only few showed GFRalpha1 immunoreactivity, indicating that GFRalpha1 may be beneficial for the survival of hippocampal neurons. The data suggest that reduced expression of GDNF and impairment of GFRalpha1/3 may contribute to hippocampal DND after focal brain ischemia.
全脑缺血后,海马CA1和CA3区锥体细胞的迟发性神经元死亡(DND)已得到广泛研究,而对于局灶性脑缺血后这个高度易损脑区的DND却知之甚少。在本研究中,我们对大鼠短暂性大脑中动脉闭塞(MCAO)后1、3、7、14和30天海马神经元凋亡的分布及时间进程进行了研究。在60%的动物中,90%以上的CA1锥体细胞在第3天显示出强烈的缺口末端标记(TUNEL)染色,其中约40%的细胞出现核碎裂和边缘化。TUNEL阳性细胞数量在接下来的几天内减少,但MCAO后30天,仍有一些凋亡神经元存在。利用三重免疫荧光和共聚焦激光扫描显微镜分析胶质细胞源性神经营养因子(GDNF)及其受体GFRalpha1、GFRalpha2和GFRalpha3的表达,发现在所有显示明显海马DND的动物中,CA1区TUNEL染色开始前,GFRalpha1、GFRalpha3和GDNF的神经元染色减少。7天后,一些凋亡神经元仍表达GFRalpha3,而只有少数显示GFRalpha1免疫反应性,这表明GFRalpha1可能对海马神经元的存活有益。数据表明,GDNF表达降低以及GFRalpha1/3受损可能导致局灶性脑缺血后海马DND。