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K+-dependent cerebellar granule neuron apoptosis. Role of task leak K+ channels
Inger Lauritzen1, Marc Zanzouri, Eric Honoré
1Institut de Pharmacologie Moléculaire et Cellulaire, CNRS, Institut Paul Hamel, 660 route des Lucioles, Sophia Antipolis, 06560 Valbonne, France.
Abstract:
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.