Lauritzen Inger, Zanzouri Marc, Honoré Eric, Duprat Fabrice, Ehrengruber Markus U, Lazdunski Michel, Patel Amanda J
Institut de Pharmacologie Moléculaire et Cellulaire, CNRS, Institut Paul Hamel, 660 route des Lucioles, Sophia Antipolis, 06560 Valbonne, France.
J Biol Chem. 2003 Aug 22;278(34):32068-76. doi: 10.1074/jbc.M302631200. Epub 2003 Jun 3.
Rat mature cerebellar granule, unlike hippocampal neurons, die by apoptosis when cultured in a medium containing a physiological concentration of K+ but survive under high external K+ concentrations. Cell death in physiological K+ parallels the developmental expression of the TASK-1 and TASK-3 subunits that encode the pH-sensitive standing outward K+ current IKso. Genetic transfer of the TASK subunits in hippocampal neurons, lacking IKso, induces cell death, while their genetic inactivation protects cerebellar granule neurons. Neuronal death of cultured rat granule neurons is also prevented by conditions that specifically reduce K+ efflux through the TASK-3 channels such as extracellular acidosis and ruthenium red. TASK leak K+ channels thus play an important role in K+-dependent apoptosis of cerebellar granule neurons in culture.
与海马神经元不同,大鼠成熟小脑颗粒细胞在含有生理浓度钾离子(K+)的培养基中培养时会通过凋亡死亡,但在高细胞外钾离子浓度下能够存活。在生理钾离子浓度下的细胞死亡与TASK-1和TASK-3亚基的发育表达平行,这两个亚基编码对pH敏感的外向钾离子电流IKso。在缺乏IKso的海马神经元中,TASK亚基的基因转移会诱导细胞死亡,而它们的基因失活则能保护小脑颗粒神经元。培养的大鼠颗粒神经元的神经元死亡也可通过特异性减少通过TASK-3通道的钾离子外流的条件来预防,如细胞外酸中毒和钌红。因此,TASK渗漏钾离子通道在培养的小脑颗粒神经元的钾离子依赖性凋亡中起重要作用。