Calcium transport and inner mitochondrial membrane damage in renal cortical mitochondria
- 1 June 1985
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Renal Physiology
- Vol. 248 (6) , F876-F889
- https://doi.org/10.1152/ajprenal.1985.248.6.f876
Abstract
Ca2+ uptake and efflux processes, as they are manifested during procedures used for isolation of renal cortical mitochondria, were characterized in order to provide a better basis for making inferences from isolated mitochondria about the in vivo state of mitochondrial Ca2+ homeostasis in both normal and injured tissues and to better define the mechanisms by which Ca2+ mediates injury to renal cortical mitochondria. Mitochondrial Ca2+ uptake predictably occurred when the capacity of the Ca2+ chelator added to the isolating medium to maintain free Ca2+ in the submicromolar range was exhausted unless ruthenium red was present to specifically inhibit the Ca2+ uniport. Ca2+ uptake during isolation ultimately led to loss of accumulated Ca2+ and intramitochondrial K+ as well as to deterioration of respiratory function. Extramitochondrial Ca2+ also evoked the latter two events in the absence of Ca2+ uptake but only at much higher medium Ca2+ levels than were required when Ca2+ uptake was allowed to occur. Studies using mitochondria loaded with known amounts of Ca2+ at 4 degrees C and then subjected to a reisolation procedure including all the steps of normal isolation demonstrated that phosphate markedly potentiated Ca2+-induced alterations of mitochondrial membrane permeability properties. Of several agents studied singly, fatty acid-free albumin was most effective in blocking Ca2+ + phosphate-induced alterations of mitochondrial membrane permeability. The protective effect of fatty acid-free albumin was further enhanced by combining it with Mg2+, dibucaine, or oligomycin + ADP. This study thus quantitatively defined conditions under which Ca2+ uptake can be expected to occur during mitochondrial isolation, demonstrated that the effects of this Ca2+ uptake on mitochondrial properties are similar to those previously elucidated in mitochondria studied at warmer temperatures, and defined methods suitable for blocking such Ca2+ movements and their deleterious effects.This publication has 19 references indexed in Scilit:
- Intramitochondrial phospholipase activity and the effects of Ca2+ plus N-ethylmaleimide on mitochondrial function.Journal of Biological Chemistry, 1979
- The Ca2+-induced membrane transition in mitochondriaArchives of Biochemistry and Biophysics, 1979
- The Ca2+-induced membrane transition in mitochondriaArchives of Biochemistry and Biophysics, 1979
- Regulation of Ca 2+ release from mitochondria by the oxidation-reduction state of pyridine nucleotidesProceedings of the National Academy of Sciences, 1978
- Abnormal mitochondrial oxidative phosphorylation of ischemic myocardium reversed by Ca2+-chelating agentsJournal of Molecular and Cellular Cardiology, 1977
- Kinetics of ATP-dependent Mg2+flux in mitochondriaBiochemistry, 1976
- Effect of Calcium Chelation on the Ion Content of Liver Mitochondria in Carbon Tetrachloride-poisoned RatsJournal of Biological Chemistry, 1968
- The Effect of Parathyroid Hormone in Vivo on the Accumulation of Calcium and Phosphate by Kidney and on Kidney Mitochondrial FunctionJournal of Biological Chemistry, 1967
- Ca++ Uptake by Rat Kidney Mitochondria and Its Dependence on Respiration and PhosphorylationJournal of Biological Chemistry, 1962
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951