Göb Eva, Bittner Stefan, Bobak Nicole, Kraft Peter, Göbel Kerstin, Langhauser Friederike, Homola György A, Brede Marc, Budde Thomas, Meuth Sven G, Kleinschnitz Christoph
Department of Neurology, University Clinics Würzburg, Würzburg, Germany.
Pflugers Arch. 2015 May;467(5):973-87. doi: 10.1007/s00424-014-1626-8. Epub 2014 Oct 15.
Potassium channels can fulfill both beneficial and detrimental roles in neuronal damage during ischemic stroke. Earlier studies have characterized a neuroprotective role of the two-pore domain potassium channels KCNK2 (TREK1) and KCNK3 (TASK1). Protective neuronal hyperpolarization and prevention of intracellular Ca(2+) overload and glutamate excitotoxicity were suggested to be the underlying mechanisms. We here identify an unexpected role for the related KCNK5 channel in a mouse model of transient middle cerebral artery occlusion (tMCAO). KCNK5 is strongly upregulated on neurons upon cerebral ischemia, where it is most likely involved in the induction of neuronal apoptosis. Hypoxic conditions elevated neuronal expression levels of KCNK5 in acute brain slices and primary isolated neuronal cell cultures. In agreement, KCNK5 knockout mice had significantly reduced infarct volumes and improved neurologic function 24 h after 60 min of tMCAO and this protective effect was preserved at later stages of infarct development. KCNK5 deficiency resulted in a significantly reduced number of apoptotic neurons, a downregulation of pro-apoptotic and upregulation of anti-apoptotic factors. Results of adoptive transfer experiments of wild-type and Kcnk5 (-/-) immune cells into Rag1 (-/-) mice prior to tMCAO exclude a major role of KCNK5 in poststroke inflammatory reactions. In summary, KCNK5 expression is induced on neurons under ischemic conditions where it most likely exerts pro-apoptotic effects. Hence, pharmacological blockade of KCNK5 might have therapeutic potential in preventing ischemic neurodegeneration.
钾通道在缺血性中风所致的神经元损伤中可发挥有益和有害两种作用。早期研究已明确双孔结构域钾通道KCNK2(TREK1)和KCNK3(TASK1)具有神经保护作用。保护性神经元超极化以及防止细胞内Ca(2+)超载和谷氨酸兴奋性毒性被认为是其潜在机制。我们在此确定了相关的KCNK5通道在短暂性大脑中动脉闭塞(tMCAO)小鼠模型中的意外作用。脑缺血时,神经元上的KCNK5强烈上调,很可能参与神经元凋亡的诱导。缺氧条件下,急性脑片和原代分离神经元细胞培养物中神经元KCNK5的表达水平升高。与此一致,KCNK5基因敲除小鼠在tMCAO 60分钟后24小时梗死体积显著减小,神经功能改善,且这种保护作用在梗死发展的后期阶段依然存在。KCNK5缺乏导致凋亡神经元数量显著减少,促凋亡因子下调,抗凋亡因子上调。在tMCAO前将野生型和Kcnk5 (-/-)免疫细胞过继转移到Rag1 (-/-)小鼠体内的实验结果排除了KCNK5在中风后炎症反应中的主要作用。总之,缺血条件下神经元上会诱导KCNK5表达,其很可能发挥促凋亡作用。因此,KCNK5的药理学阻断在预防缺血性神经变性方面可能具有治疗潜力。