Regulation of Na+/H+ and Cl−/HCO3− antiports in vero cells

Publisher Website
Google Scholar
Abstract
The effect of serum, phorbol‐12‐myristate‐13‐acetate (TPA), and forskolin on the activity Na+/H+ antiport and the Na+‐coupled and Na+‐independent Cl−/ HCO3− antiport was studied in Vero cells by measuring 22Na+ and 36Cl− fluxes and changes in cytosolic pH (pHi). The Na+‐independent Cl−/HCO3− antiport, which acts as an acidifying mechanism, is strongly pH‐sensitive. In serum‐starved cells it is activated at alkaline cytosolic pH, with a half‐maximal activity at pHi ∼7.20. Incubation with serum increased the activity of the Na+‐independent Cl−/HCO3− antiport at pHi values from 6.8 to 7.2. Thus serum appeared to alter the pHi sensitivity of this antiporter such that the threshold value for activation of the antiport was shifted to a more acidic value. Na+ /H+ antiport was somewhat stimulated initially by addition of serum, but further incubation with serum (> 45 min) decreased its activity. The activity of the Na+ ‐coupled Cl−/HCO3− antiport, which is the major alkalinizing antiport in Vero cells, was not altered by short‐term incubation with serum (< 10 min) but decreased after prolonged incubation (> 45 min). Our findings with TPA and forskolin indicate that the effect of serum is partly mediated by the protein kinase C pathway, whereas the cyclic adenosine monophosphate pathway does not appear to play an important role. The net effect of serum on the pHi‐regulating antiports was a slight decrease in intracellular pH.