Essential role of aralar in the transduction of small Ca2+ signals to neuronal mitochondria

J Biol Chem. 2006 Jan 13;281(2):1039-47. doi: 10.1074/jbc.M507270200. Epub 2005 Nov 3.

Abstract

Aralar, the neuronal Ca(2+)-binding mitochondrial aspartate-glutamate carrier, has Ca(2+) binding domains facing the extramitochondrial space and functions in the malate-aspartate NADH shuttle (MAS). Here we showed that MAS activity in brain mitochondria is stimulated by extramitochondrial Ca(2+) with an S(0.5) of 324 nM. By employing primary neuronal cultures from control and aralar-deficient mice and NAD(P)H imaging with two-photon excitation microscopy, we showed that lactate utilization involves a substantial transfer of NAD(P)H to mitochondria in control but not aralar-deficient neurons, in agreement with the lack of MAS activity associated with aralar deficiency. The increase in mitochondrial NAD(P)H was greatly potentiated by large [Ca(2+)](i) signals both in control and aralar-deficient neurons, showing that these large signals activate the Ca(2+) uniporter and mitochondrial dehydrogenases but not MAS activity. On the other hand, small [Ca(2+)](i) signals potentiate the increase in mitochondrial NAD(P)H only in control but not in aralar-deficient neurons. We concluded that neuronal MAS activity is selectively activated by small Ca(2+) signals that fall below the activation range of the Ca(2+) uniporter and plays an essential role in mitochondrial Ca(2+) signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Brain / metabolism
  • Calcium / metabolism*
  • Cells, Cultured
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Genotype
  • Lactates / chemistry
  • Male
  • Membrane Transport Proteins / chemistry*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Membrane Transport Proteins / physiology*
  • Mice
  • Microscopy
  • Mitochondria / metabolism*
  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Proteins / chemistry*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mitochondrial Proteins / physiology*
  • Models, Biological
  • Muscle, Skeletal / metabolism
  • NADP / metabolism
  • Neurons / metabolism*
  • Photons
  • Polymerase Chain Reaction
  • Pyruvates / chemistry
  • Pyruvates / metabolism
  • Rats
  • Rats, Wistar
  • Signal Transduction
  • Time Factors

Substances

  • Lactates
  • Membrane Transport Proteins
  • Mitochondrial Membrane Transport Proteins
  • Mitochondrial Proteins
  • Pyruvates
  • Slc25a12 protein, mouse
  • Slc25a12 protein, rat
  • NADP
  • DNA
  • Calcium