Opposite effects of pH on open-state probability and single channel conductance of Kir4.1 channels

被引:43
作者
Yang, ZJ [1 ]
Jiang, C [1 ]
机构
[1] Georgia State Univ, Dept Biol, Atlanta, GA 30302 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1999年 / 520卷 / 03期
关键词
D O I
10.1111/j.1469-7793.1999.00921.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. A decrease in intracellular pH (pH(i)) inhibits whole-cell Kir4.1 currents. To understand channel biophysical properties underlying this inhibition, single channel Kir4.1 currents were studied in inside-out patches using symmetric concentrations of K+ applied to each side of the plasma membrane. Under such conditions, inward rectifying currents were observed in about 2 of 3 patches. At pH 7.4, these currents showed a single channel conductance of 22 pS with a channel open-state probability (P-open) of similar to 0.9. 2. The effects of intracellular protons on macroscopic Kir4.1 currents were examined in giant inside-out patches at various pH levels of internal solutions. Current amplitude increased with a modest acidification (pH 7.0 and 6.6), and decreased with further reductions in pH(i). The Kir4.1. currents were completely suppressed at pH 5.4. These effects were fast and reversible. 3. Low pH(i) inhibited P-open and enhanced single channel conductance in a concentration dependent manner with pK (midpoint pH value for channel inhibition) of 6.0 and 6.8, respectively At pH 5.8, P-open was inhibited by 70% and single channel conductance increased by 35%. Washout brought both P-open and single channel conductance rapidly back to baseline levels. 4. Theoretical currents were calculated using percentage changes in P-open and single channel conductance at each pH level tested. The trajectory of these currents is very close to that of experimental currents recorded from giant patches. Thus, opposite effects of intracellular protons on P-open and single channel conductance are demonstrated, which are likely to result in changes of macroscopic Kir4.1 currents with low pH.
引用
收藏
页码:921 / 927
页数:7
相关论文
共 25 条
[1]  
BOND CT, 1994, RECEPTOR CHANNEL, V2, P183
[2]   CLONING AND EXPRESSION OF 2 BRAIN-SPECIFIC INWARDLY RECTIFYING POTASSIUM CHANNELS [J].
BREDT, DS ;
WANG, TL ;
COHEN, NA ;
GUGGINO, WB ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (15) :6753-6757
[3]   A conserved cytoplasmic region of ROMK modulates pH sensitivity, conductance, and gating [J].
Choe, H ;
Zhou, H ;
Palmer, LG ;
Sackin, H .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 273 (04) :F516-F529
[4]   Regulation of IRK3 inward rectifier K+ channel by m1 acetylcholine receptor and intracellular magnesium [J].
Chuang, HH ;
Jan, YN ;
Jan, LY .
CELL, 1997, 89 (07) :1121-1132
[5]   Inhibition of an inward rectifier potassium channel (Kim2.3) by G-protein beta gamma subunits [J].
Cohen, NA ;
Sha, Q ;
Makhina, EN ;
Lopatin, AN ;
Linder, ME ;
Snyder, SH ;
Nichols, CG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32301-32305
[6]   Binding of the inward rectifier K+ channel Kir 2.3 to PSD-95 is regulated by protein kinase A phosphorylation [J].
Cohen, NA ;
Brenman, JE ;
Snyder, SH ;
Bredt, DS .
NEURON, 1996, 17 (04) :759-767
[7]   IDENTIFICATION AND MOLECULAR LOCALIZATION OF A PH-SENSING DOMAIN FOR THE INWARD RECTIFIER POTASSIUM CHANNEL HIR [J].
COULTER, KL ;
PERIER, F ;
RADEKE, CM ;
VANDENBERG, CA .
NEURON, 1995, 15 (05) :1157-1168
[8]   Identification of a titratable lysine residue that determines sensitivity of kidney potassium channels (ROMK) to intracellular pH [J].
Fakler, B ;
Schultz, JH ;
Yang, J ;
Schulte, U ;
Brandle, U ;
Zenner, HP ;
Jan, LY ;
Ruppersberg, JP .
EMBO JOURNAL, 1996, 15 (16) :4093-4099
[9]   Protein kinase C inhibition of cloned inward rectifier (HRK1/K(IR)2.3) K+ channels expressed in Xenopus oocytes [J].
Henry, P ;
Pearson, WL ;
Nichols, CG .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 495 (03) :681-688
[10]   Direct activation of inward rectifier potassium channels by PIP2 and its stabilization by Gβγ [J].
Huang, CL ;
Feng, SY ;
Hilgemann, DW .
NATURE, 1998, 391 (6669) :803-806