Key result
Blocking voltage-dependent potassium channels dose-dependently decreases odontoblast mineralization efficiency.
Why the study?
The precise properties of K+ currents activated by depolarization in odontoblasts remain to be elucidated.
Odontoblasts express voltage-dependent potassium channels that play an important role in dentin formation and mineralization.
Answers are grounded in this paper and cite their sources.
Leaves open any clinical relevance of Kv channels in mineralization; extends basic evidence for ion channel roles in odontoblast function.
Increased intracellular free Ca2+ concentrations elicit plasma membrane depolarization, which leads to the activation of K+ currents. However, the precise properties of K+ currents activated by depolarization in odontoblasts remain to be elucidated. The present study identified biophysical and pharmacological characteristics of time-dependent and voltage-activated K+ currents in freshly dissociated rat odontoblasts using patch-clamp recordings in a whole-cell configuration. Using a holding potential of -70 mV, outwardly rectifying time- and voltage-dependent currents were activated by depolarizing voltage. To record pure K+ conductance, we substituted Cl- in both the extracellular and intracellular solutions with gluconate-. Under these conditions, observation of K+ concentration changes in the extracellular solution showed that reversal potentials of tail currents shifted according to the K+ equilibrium potential. The activation kinetics of outward K+ currents were relatively slow and depended on the membrane potential. Kinetics of steady-state inactivation were fitted by a Boltzmann function. The half-maximal inactivation potential was -38 mV. Tetraethylammonium chloride, 4-aminopyridine, and α-dendrotoxin inhibited outward currents in odontoblasts in a concentration-dependent manner, suggesting that rat odontoblasts express the α-subunit of the time- and voltage-dependent K+ channel (Kv) subtypes Kv1.1, 1.2, and/or 1.6. We further examined the effects of Kv activity on mineralization by alizarin Red and von Kossa staining. Continuous application of tetraethylammonium chloride to human odontoblasts grown in a mineralization medium over a 21-day period exhibited a dose-dependent decrease in mineralization efficiency compared to cells without tetraethylammonium chloride. This suggests that odontoblasts functionally express voltage-dependent K+ channels that play important roles in dentin formation.
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Kojima et al. (2017) studied Odontoblast electrophysiology. Potassium channel blockers (TEA, 4-AP, αDTX) vs. Control (no blocker) was evaluated on Peak outward K+ current amplitude and mineralization efficiency. Odontoblasts functionally express voltage-dependent K+ channels (Kv1.1, 1.2, and/or 1.6), and their blockade by tetraethylammonium chloride dose-dependently decreases mineralization efficiency.
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