Department of Physiology, Shanxi Medical University, Taiyuan 030001, China.
Neurosci Lett. 2012 Jun 19;518(2):92-5. doi: 10.1016/j.neulet.2012.04.060. Epub 2012 May 3.
Hippocampal CA1 pyramidal neurons are sensitive to ischemic damage. However, the cellular and molecular mechanisms underlying neuronal cell death caused by ischemia-reperfusion (I/R) are not completely clear. Here, we report that the ephrinA/EphA cell-cell interaction signaling pathway plays an important role in the apoptosis of hippocampal CA1 pyramidal neurons induced by I/R. We found that the expression of ephrinA3 and EphA4 is increased in the CA1 region following transient forebrain ischemia. Blocking ephrinA3/EphA4 interaction by EphA4-Fc, an inhibitor of EphA4, attenuated apoptotic neuronal cell death, likely through the inhibition of caspase-3 activation. These results reveal a novel function of ephrin/Eph signaling in the regulation of apoptosis in CA1 pyramidal neurons after I/R.
海马 CA1 锥体神经元对缺血损伤敏感。然而,缺血再灌注(I/R)引起神经元细胞死亡的细胞和分子机制尚不完全清楚。在这里,我们报告称,ephrinA/EphA 细胞-细胞相互作用信号通路在 I/R 诱导的海马 CA1 锥体神经元凋亡中发挥重要作用。我们发现,短暂性前脑缺血后 CA1 区 ephrinA3 和 EphA4 的表达增加。EphA4-Fc(EphA4 的抑制剂)阻断 ephrinA3/EphA4 相互作用,可减轻凋亡性神经元细胞死亡,可能是通过抑制半胱氨酸天冬氨酸蛋白酶-3 的激活。这些结果揭示了 ephrin/Eph 信号在 I/R 后 CA1 锥体神经元凋亡调节中的新功能。