Inositol 1,4,5-trisphosphate receptor/GAPDH complex augments Ca2+ release via locally derived NADH

Proc Natl Acad Sci U S A. 2005 Feb 1;102(5):1357-9. doi: 10.1073/pnas.0409657102. Epub 2005 Jan 26.

Abstract

NADH regulates the release of calcium from the endoplasmic reticulum by modulation of inositol 1,4,5-trisphosphate receptors (IP3R), accounting for the augmented calcium release of hypoxic cells. We report selective binding of IP3R to GAPDH, whose activity leads to the local generation of NADH to regulate intracellular calcium signaling. This interaction requires cysteines 992 and 995 of IP3R and C150 of GAPDH. Addition of native GAPDH and NAD+ to WT IP3R stimulates calcium release, whereas no stimulation occurs with C992S/995S IP3R that cannot bind GAPDH. Thus, the IP3R/GAPDH interaction likely enables cellular energy dynamics to impact calcium signaling.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • COS Cells
  • Calcium / metabolism*
  • Calcium Channels / chemistry
  • Calcium Channels / genetics
  • Calcium Channels / metabolism*
  • Cell Line
  • Chlorocebus aethiops
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) / chemistry
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) / genetics
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) / metabolism*
  • Humans
  • Inositol 1,4,5-Trisphosphate Receptors
  • Mutagenesis, Site-Directed
  • NAD / metabolism*
  • PC12 Cells
  • Peptide Fragments / chemistry
  • Rats
  • Receptors, Cytoplasmic and Nuclear / chemistry
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Recombinant Proteins / metabolism

Substances

  • Calcium Channels
  • ITPR1 protein, human
  • Inositol 1,4,5-Trisphosphate Receptors
  • Peptide Fragments
  • Receptors, Cytoplasmic and Nuclear
  • Recombinant Proteins
  • NAD
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)
  • Calcium