Key result
Extracellular Ca2+ modulates T-type Ca2+ channel function by competing with protons for binding to surface charges and the selectivity filter, counteracting proton-induced modifications of channel activation.
Extracellular Ca2+ modulates T-type calcium channel function by competing with protons for surface charges and the selectivity filter, providing mechanistic insight into ionic modulation of channel gating.
Hypothesis-generating for T-type channel modulation in cardiac excitability; leaves open translation to human physiology or therapy.
Since Ca2+ is a major competitor of protons for the modulation of high voltage-activated Ca2+ channels, we have studied the modulation by extracellular Ca2+ of the effects of proton on the T-type Ca2+ channel alpha1G (CaV3.1) expressed in HEK293 cells. At 2 mM extracellular Ca2+ concentration, extracellular acidification in the pH range from 9.1 to 6.2 induced a positive shift of the activation curve and increased its slope factor. Both effects were significantly reduced if the concentration was increased to 20 mM or enhanced in the absence of Ca2+. Extracellular protons shifted the voltage dependence of the time constant of activation and decreased its voltage sensitivity, which excludes a voltage-dependent open pore block by protons as the mechanism modifying the activation curve. Changes in the extracellular pH altered the voltage dependence of steady-state inactivation and deactivation kinetics in a Ca2+-dependent manner, but these effects were not strictly correlated with those on activation. Model simulations suggest that protons interact with intermediate closed states in the activation pathway, decreasing the gating charge and shifting the equilibrium between these states to less negative potentials, with these effects being inhibited by extracellular Ca2+. Extracellular acidification also induced an open pore block and a shift in selectivity toward monovalent cations, which were both modulated by extracellular Ca2+ and Na+. Mutation of the EEDD pore locus altered the Ca2+-dependent proton effects on channel selectivity and permeation. We conclude that Ca2+ modulates T-type channel function by competing with protons for binding to surface charges, by counteracting a proton-induced modification of channel activation and by competing with protons for binding to the selectivity filter of the channel.
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Talavera et al. (2003) studied this question. Extracellular acidification and varying extracellular Ca2+ concentrations vs. Alkaline pH (9.1) and standard Ca2+ concentrations was evaluated on Voltage dependence of channel activation, steady-state inactivation, and open pore conduction. Extracellular Ca2+ modulates T-type Ca2+ channel function by competing with protons for binding to surface charges and the selectivity filter, counteracting proton-induced modifications of channel activation.
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