K+-dependent cerebellar granule neuron apoptosis -: Role of task leak K+ channels

被引:165
作者
Lauritzen, I
Zanzouri, M
Honoré, E
Duprat, F
Ehrengruber, MU
Lazdunski, M
Patel, AJ
机构
[1] Inst Paul Hamel, CNRS, Inst Pharmacol Mol & Cellulaire, F-06560 Valbonne, France
[2] Univ Zurich, Brain Res Inst, CH-8057 Zurich, Switzerland
关键词
D O I
10.1074/jbc.M302631200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:32068 / 32076
页数:9
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