Decrease in Na(+)-K(+)-ATPase associated with maturation of sheep reticulocytes

Abstract

Na(+)-K(+)-ATPase of immature and mature sheep red blood cells of both the high-K+ and low-K+ genotype and of immature cells matured in vitro was detected using polyclonal antiserum to purified sheep kidney Na(+)-K(+)-ATPase. This antiserum detects both alpha (alpha 1)- and alpha + (alpha 2 and/or alpha 3)-isoforms of the catalytic subunit as well as the beta-subunit of brain and kidney Na(+)-K(+)-ATPase. After sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting, a single major immunologically reactive component corresponding to the alpha-subunit was detected in membranes of immature and mature cells from sheep of both genotypes. Cells separated according to increasing density showed a corresponding decrease in ouabain binding sites on the cells and Na(+)-activated ATP hydrolysis of membranes isolated from the cells. A progressive decrease in immunologically reactive alpha-subunit was also observed. After in vitro culture of reticulocytes, reduction in ouabain binding to the cells was also associated with loss in alpha-subunit. As well, appearance of immunologically reactive alpha-subunit was detected in membranous material shed into the incubation medium, accounting for a fraction (less than or equal to 30%) of the material lost from the cells. Proteolytic sensitivity of the alpha-subunit indicates that, in this material, the cytoplasmic surface of the enzyme is exposed to the medium. The shed material was largely devoid of function as evidenced in little, if any, Na(+)-dependent phosphorylation of Na(+)-K(+)-ATPase. The existence in reticulocytes of an intracellular pool of ouabain binding sites was indicated by the transient appearance on the cell surface of ouabain binding sites after rapid ATP depletion and also after addition of chloroquine to cells during culture. Taken together, these findings indicate that the maturation-associated loss of sodium pump protein involves, at least partly, energy-dependent endocytosis and, presumably, processing whereby inactivation of function occurs as well as release of pump protein into the extracellular milieu.