TY - JOUR
T1 - Correlation of the effect of Ca+2 on Na+ and K+ permeability and membrane potential of Ehrlich ascites tumor cells
AU - Smith, Thomas C.
AU - Vernon, Kim D.
PY - 1979/2
Y1 - 1979/2
N2 - The effect of Ca+2 on the transport and intracellular distribution of Na+ and K+ in Ehrlich ascites tumor cells was investigated in an effort to establish the mechanism of Ca+2‐induced hyperpolarization of the cell membrane. Inclusion of Ca+2 (2mM) in the incubation medium leads to reduced cytoplasmic concentrations of Na+, K+ and Cl− in steady state cells. In cells inhibited by ouabain, Ca+2 causes a 41% decrease in the rate of net K+ loss, but is without effect on the rate of net Na+ accumulation. Net K+ flux is reduced by 50%, while net Na+ flux is unchanged in the transport‐inhibited cells. The membrane potential of cells in Ca+2‐free medium (‐13.9 ± 0.8 mV) is unaffected by the addition of ouabain. However, the potential of cells in Ca+2‐containing medium (‐23.3 ± 1.2 mV) declines in one hour after the addition of ouabain to values comparable to those of control cells (‐15.2 ± 0.7 mV). The results of these experiment are consistent with the postulation that Ca+2 exerts two effects on Na+ and K+ transport. First, Ca+2 reduces the membrane permeability to K+ by 25%. Second, Ca+2 alters the coupling of the Na/K active transport mechanism leding to an electrogenic hyperpolarization of the membrane.
AB - The effect of Ca+2 on the transport and intracellular distribution of Na+ and K+ in Ehrlich ascites tumor cells was investigated in an effort to establish the mechanism of Ca+2‐induced hyperpolarization of the cell membrane. Inclusion of Ca+2 (2mM) in the incubation medium leads to reduced cytoplasmic concentrations of Na+, K+ and Cl− in steady state cells. In cells inhibited by ouabain, Ca+2 causes a 41% decrease in the rate of net K+ loss, but is without effect on the rate of net Na+ accumulation. Net K+ flux is reduced by 50%, while net Na+ flux is unchanged in the transport‐inhibited cells. The membrane potential of cells in Ca+2‐free medium (‐13.9 ± 0.8 mV) is unaffected by the addition of ouabain. However, the potential of cells in Ca+2‐containing medium (‐23.3 ± 1.2 mV) declines in one hour after the addition of ouabain to values comparable to those of control cells (‐15.2 ± 0.7 mV). The results of these experiment are consistent with the postulation that Ca+2 exerts two effects on Na+ and K+ transport. First, Ca+2 reduces the membrane permeability to K+ by 25%. Second, Ca+2 alters the coupling of the Na/K active transport mechanism leding to an electrogenic hyperpolarization of the membrane.
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U2 - 10.1002/jcp.1040980212
DO - 10.1002/jcp.1040980212
M3 - Article
C2 - 570569
AN - SCOPUS:0018417306
VL - 98
SP - 359
EP - 369
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
SN - 0021-9541
IS - 2
ER -