Characterization of distinct single-channel properties of Ca²⁺ inward currents in mitochondria

Pflugers Arch. 2013 Jul;465(7):997-1010. doi: 10.1007/s00424-013-1224-1. Epub 2013 Feb 9.

Abstract

Previous studies have demonstrated several molecularly distinct players involved in mitochondrial Ca(2+) uptake. In the present study, electrophysiological recordings on mitoplasts that were isolated from HeLa cells were performed in order to biophysically and pharmacologically characterize Ca(2+) currents across the inner mitochondrial membrane. In mitoplast-attached configuration with 105 mM Ca(2+) as a charge carrier, three distinct channel conductances of 11, 23, and 80 pS were observed. All types of mitochondrial currents were voltage-dependent and essentially depended on the presence of Ca(2+) in the pipette. The 23 pS channel exhibited burst kinetics. Though all channels were sensitive to ruthenium red, their sensitivity was different. The 11 and 23 pS channels exhibited a lower sensitivity to ruthenium red than the 80 pS channel. The activities of all channels persisted in the presence of cylosporin A, CGP 37187, various K(+)-channel inhibitors, and Cl(-) channel blockers disodium 4,4'-diisothiocyanatostilbene-2,2'-disulfonate and niflumic acid. Collectively, our data identified multiple conductances of Ca(2+) currents in mitoplasts isolated from HeLa cells, thus challenging the dogma of only one unique mitochondrial Ca(2+) uniporter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials*
  • Calcium / metabolism*
  • Calcium Channels / classification
  • Calcium Channels / drug effects
  • Calcium Channels / metabolism*
  • Cyclosporine / pharmacology
  • HeLa Cells
  • Humans
  • Kinetics
  • Mitochondrial Membranes / metabolism*
  • Potassium Channel Blockers / pharmacology
  • Ruthenium Red / pharmacology

Substances

  • Calcium Channels
  • Potassium Channel Blockers
  • Ruthenium Red
  • Cyclosporine
  • Calcium