Coulson Elizabeth J, May Linda M, Osborne Shona L, Reid Kate, Underwood Clare K, Meunier Frederic A, Bartlett Perry F, Sah Pankaj
Queensland Brain Institute and School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia.
J Neurosci. 2008 Jan 2;28(1):315-24. doi: 10.1523/JNEUROSCI.2699-07.2008.
The pan neurotrophin receptor p75(NTR) signals programmed cell death both during nervous system development and after neural trauma and disease in the adult. However, the molecular pathways by which death is mediated remain poorly understood. Here, we show that this cell death is initiated by activation of G-protein-coupled inwardly rectifying potassium (GIRK/Kir3) channels and a consequent potassium efflux. Death signals stimulated by neurotrophin-mediated cleavage of p75(NTR) activate GIRK channels through the generation and binding of phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2/PIP2] to GIRK channels. Both GIRK channel activity and p75(NTR)-mediated neuronal death are inhibited by sequestration of PtdIns(4,5)P2 and application of GIRK channel inhibitors, whereas pertussis toxin treatment has no effect. Thus, p75(NTR) activates GIRK channels without the need for G(i/o)-proteins. Our results demonstrate a novel mode of activation of GIRK channels, representing an early step in the p75(NTR)-mediated cell death pathway and suggesting a function for these channels during nervous system development.
泛神经营养因子受体p75(NTR)在神经系统发育过程中以及成体神经创伤和疾病后均介导程序性细胞死亡。然而,介导细胞死亡的分子途径仍知之甚少。在此,我们表明这种细胞死亡是由G蛋白偶联内向整流钾通道(GIRK/Kir3)的激活以及随之而来的钾外流引发的。神经营养因子介导的p75(NTR)裂解所刺激的死亡信号通过磷脂酰肌醇4,5-二磷酸[PtdIns(4,5)P2/PIP2]的生成和与GIRK通道的结合来激活GIRK通道。PtdIns(4,5)P2的螯合和GIRK通道抑制剂的应用均抑制GIRK通道活性和p75(NTR)介导的神经元死亡,而百日咳毒素处理则无作用。因此,p75(NTR)无需G(i/o)蛋白即可激活GIRK通道。我们的结果证明了GIRK通道激活的一种新模式,代表了p75(NTR)介导的细胞死亡途径中的早期步骤,并提示了这些通道在神经系统发育过程中的功能。