Modulation of the heteromeric Kir4.1-Kir5.1 channels by P-CO2 at physiological levels

Citation
N. Cui et al., Modulation of the heteromeric Kir4.1-Kir5.1 channels by P-CO2 at physiological levels, J CELL PHYS, 189(2), 2001, pp. 229-236
Citations number
27
Categorie Soggetti
Cell & Developmental Biology
Journal title
JOURNAL OF CELLULAR PHYSIOLOGY
ISSN journal
00219541 → ACNP
Volume
189
Issue
2
Year of publication
2001
Pages
229 - 236
Database
ISI
SICI code
0021-9541(200111)189:2<229:MOTHKC>2.0.ZU;2-V
Abstract
Several inward rectifier K+ NO channels are pH-sensitive, making them poten tial candidates for CO2 chemoreception in cells. However, there is no evide nce showing that Kir channels change their activity at near physiological l evel of P-CO2, as most previous studies were done using high concentrations Of CO2. It is known that the heteromeric Kir4.1-Kir5.1 channels are highly sensitive to intracellular protons with pKa value right at the physiologic al pH level. Such a pKa value may allow these channels to regulate membrane potentials with modest changes in P-CO2,. To test this hypothesis, we stud ied the Kir4.1-Kir5.1 currents expressed in Xenopus oocytes and membrane po tentials in the presence and absence of bicarbonate. Evident inhibition of these currents (by similar to5%) was seen with P-CO2 as low as 8 torr. High er P-CO2 levels (23-60 torr) produced stronger inhibitions (by 30-40%). The inhibitions led to graded depolarizations (5-45 mV with P-CO2 8-60 torr). Similar effects were observed in the presence of 24 mM bicarbonate and 5% C O2. Indeed, the Kir4.1-Kir5.1 currents were enhanced with 3% CO2 and suppre ssed with 8% CO2 in voltage clamp, resulting in hyper- (-9 mV) and depolari zation (16 mV) in current clamp, respectively. With physiological concentra tion of extracellular K+, the Kir4.1-Kir5.1 channels conduct substantial ou tward currents that were similarly inhibited by CO2 as their inward rectify ing currents. These results therefore indicate that the heteromeric Kir4.1- Kir5.1 channels are modulated by a modest change in P-CO2 levels. Such a mo dulation alters cellular excitability, and enables the cell to detect hyper capnia and hypocapnia in the presence of bicarbonate. (C) 2001 Wiley-Liss, Inc.