par Sohraby, Sarah 
;Fisher, Richard R.S.;Abramow, Maurice ;Mies, Frédérique
Référence The Journal of biological chemistry, 268, 35, page (26613-26617)
Publication Publié, 1993-12
;Fisher, Richard R.S.;Abramow, Maurice ;Mies, Frédérique Référence The Journal of biological chemistry, 268, 35, page (26613-26617)
Publication Publié, 1993-12
Article révisé par les pairs
| Résumé : | Aldosterone treatment of A6 cultured renal epithelial cells methylates the apical membrane, and we examined the aldosterone-induced carboxymethylation of the apical membrane of these cells to determine the targeted polypeptides. Methionine-deprived A6 cells were incubated with aldosterone and [3H]methionine. Homogenates and apical membranes were solubilized and analyzed by SDS-polyacrylamide gel electrophoresis. Label incorporation in a 90-kDa polypeptide was more intense (4-fold) in membranes after aldosterone compared to control. For in vitro methylation, membranes were isolated, incubated with S-adenosyl-L-[methyl-3H]methionine, and analyzed for 3H-methyl uptake. Label incorporation was low in control membranes but markedly stimulated (4-fold) in membrane preparations from aldosterone-treated cells. Guanosine 5′-O-(3-thiotriphosphate) increased in vitro methylation of a 90-kDa polypeptide 5-fold in control membranes but after aldosterone, where methylation was already stimulated, little change was observed. We conclude that aldosterone induces methylation of an apical membrane 90-kDa polypeptide, possibly a subunit of the epithelial Na+ channel, in a GTP-dependent manner, and this may be one of the final steps in a cascade of reactions leading to the natriferic action of this hormone. |
