TY - JOUR
T1 - ATP is a coupling modulator of parallel Na,K-ATPase-K-channel activity in the renal proximal tubule
AU - Tsuchiya, K.
AU - Wang, W.
AU - Giebisch, G.
AU - Welling, P. A.
PY - 1992
Y1 - 1992
N2 - A fundamental and essential property of nearly all salt-transporting epithelia is the tight parallel coupling between the magnitude of the K- conductive pathway at the basolateral membrane and the activity of the Na,K- dependent ATPase (Na,K-ATPase). In the present study, we demonstrate that the coupling response in the renal proximal tubule is governed, at least in part, through the interaction between ATP-sensitive K channels and Na,K-ATPase- mediated changes in intracellular ATP levels. First, we identified a K- selective channel at the basolateral membrane, which is inhibited by the cytosolic addition of ATP. Second, conventional microelectrode analysis in the isolated perfused proximal straight tubule revealed that these channels are the major determinant of the macroscopic K conductance so that ATP- mediated changes in the open probability of the K channel could alter the extent of K recycling. Indeed, the increase in the macroscopic K conductance upon stimulation of transcellular Na transport and pump activity was found to be paralleled by a decrease in intracellular ATP. Finally, a causal link between parallel Na,K-ATPase-K-channel activity and ATP was established by the finding that intracellular ATP loading uncoupled the response. With our recent observations that similar ATP-sensitive K channels are expressed abundantly in other epithelia, we postulate that ATP may act as a universal coupling modulator of parallel Na,K-ATPase-K-channel activity.
AB - A fundamental and essential property of nearly all salt-transporting epithelia is the tight parallel coupling between the magnitude of the K- conductive pathway at the basolateral membrane and the activity of the Na,K- dependent ATPase (Na,K-ATPase). In the present study, we demonstrate that the coupling response in the renal proximal tubule is governed, at least in part, through the interaction between ATP-sensitive K channels and Na,K-ATPase- mediated changes in intracellular ATP levels. First, we identified a K- selective channel at the basolateral membrane, which is inhibited by the cytosolic addition of ATP. Second, conventional microelectrode analysis in the isolated perfused proximal straight tubule revealed that these channels are the major determinant of the macroscopic K conductance so that ATP- mediated changes in the open probability of the K channel could alter the extent of K recycling. Indeed, the increase in the macroscopic K conductance upon stimulation of transcellular Na transport and pump activity was found to be paralleled by a decrease in intracellular ATP. Finally, a causal link between parallel Na,K-ATPase-K-channel activity and ATP was established by the finding that intracellular ATP loading uncoupled the response. With our recent observations that similar ATP-sensitive K channels are expressed abundantly in other epithelia, we postulate that ATP may act as a universal coupling modulator of parallel Na,K-ATPase-K-channel activity.
KW - epithelia
KW - kidney
KW - patch clamp
KW - pump-leak coupling
KW - signal transduction
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U2 - 10.1073/pnas.89.14.6418
DO - 10.1073/pnas.89.14.6418
M3 - Article
C2 - 1321439
AN - SCOPUS:0026652559
SN - 0027-8424
VL - 89
SP - 6418
EP - 6422
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 14
ER -