Key result
Increasing PCO2 increased the open probability of an inwardly rectifying K+ channel in HeLa cells, independent of extracellular pH.
The study identifies a CO2-sensitive inwardly rectifying K+ channel that increases its open probability with rising PCO2 at constant pH, providing a potential mechanism for CO2-dependent hyperpolarization.
Does not support clinical translation; leaves open the channel's physiological role in CO2 sensing in vivo.
CO(2) chemosensing is a vital function for the maintenance of life that helps to control acid-base balance. Most studies have reported that CO(2) is measured via its proxy, pH. Here we report an inwardly rectifying channel, in outside-out excised patches from HeLa cells that was sensitive to modest changes in PCO(2) under conditions of constant extracellular pH. As PCO(2) increased, the open probability of the channel increased. The single-channel currents had a conductance of 6.7 pS and a reversal potential of -70 mV, which lay between the K(+) and Cl(-) equilibrium potentials. This reversal potential was shifted by +61 mV following a tenfold increase in extracellular [K(+)] but was insensitive to variations of extracellular [Cl(-)]. The single-channel conductance increased with extracellular [K(+)]. We propose that this channel is a member of the Kir family. In addition to this K(+) channel, we found that many of the excised patches also contained a conductance carried via a Cl(-)-selective channel. This CO(2)-sensitive Kir channel may hyperpolarize excitable cells and provides a potential mechanism for CO(2)-dependent inhibition during hypercapnia.
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Huckstepp et al. (2011) studied this question. Elevated PCO2 vs. 35 mmHg PCO2 was evaluated on Channel open probability (Po). Increasing PCO2 increased the open probability of an inwardly rectifying K+ channel in HeLa cells, independent of extracellular pH.
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