ENZYMATIC AND FUNCTIONAL EVIDENCE FOR ADAPTATION OF THE VACUOLAR H-ATPASE IN PROXIMAL TUBULE APICAL MEMBRANES FROM RATS WITH CHRONIC METABOLIC-ACIDOSIS()

Citation
R. Chambrey et al., ENZYMATIC AND FUNCTIONAL EVIDENCE FOR ADAPTATION OF THE VACUOLAR H-ATPASE IN PROXIMAL TUBULE APICAL MEMBRANES FROM RATS WITH CHRONIC METABOLIC-ACIDOSIS(), The Journal of biological chemistry, 269(5), 1994, pp. 3243-3250
Citations number
44
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
269
Issue
5
Year of publication
1994
Pages
3243 - 3250
Database
ISI
SICI code
0021-9258(1994)269:5<3243:EAFEFA>2.0.ZU;2-P
Abstract
The present work examined the effects of chronic metabolic acidosis on the vacuolar proton-translocating adenosine triphosphatase (H+-ATPase ) activity both in rat renal cortical homogenates and in their luminal membranes. Moreover, to assess the effect of acidosis on H+ transport by the apical H+-ATPase, we have developed a detergent-dilution proce dure, resulting in the formation of sealed vesicles having this enzyme at their external surface. NH4Cl loading for 4 days had no effect on homogenates H+-ATPase activity, estimated with either N-ethylmaleimide or bafilomycin A1. In contrast, H+-ATPase activities were increased s ignificantly by about 30% in both native apical membranes prepared by Ca2+ aggregation and detergent-treated luminal vesicles from acidotic animal. Kinetic analysis revealed that this stimulation was solely thr ough changes in the V(max) for ATP. In membranes prepared by Mg2+ aggr egation, acidosis also caused significant stimulation of the H+ATPase activity. In addition, the initial rate of ATP-induced intravesicular acidification was 25% higher in reoriented H+-ATPase vesicles from aci dotic rats, whereas passive proton permeability was identical in both groups. Finally, both vesicle enrichments and yields of luminal marker s and de-enrichments and yields of intracellular membrane markers were identical in the two groups. These results provide enzymatic and func tional evidence suggesting that chronic acidosis induces an adaptative change in the rat brush border H+-ATPase.