Extracellular reactive oxygen species are generated by a plasma membrane oxidative phosphorylation system

Free Radic Biol Med. 2017 Nov:112:504-514. doi: 10.1016/j.freeradbiomed.2017.08.016. Epub 2017 Aug 24.

Abstract

Although the oxidative phosphorylation (OXPHOS) system has been found in mitochondria and the plasma membrane of various mammalian cell lines, understanding the physiological functions of the plasma membrane OXPHOS system is challenging. Here, we demonstrated that OXPHOS I, II, III, IV and V subunits were expressed in the plasma membrane of HepG2 cells and primary mouse hepatocytes, as determined by non-permeabilized immunofluorescence, total internal reflection fluorescence (TIRF) microscopy, cell surface-biotin labeling and plasma membrane and lipid raft isolation. Next, we demonstrated that NADH administration generated extracellular superoxide and improved insulin signaling in HepG2 cells and primary mouse hepatocytes. The NADH-dependent generation of extracellular superoxide was prevented by knockdown of NDUFV-1, the first subunit of OXPHOS I receiving electrons from NADH and the NADH-improved insulin signaling was abolished by extracellular catalase. Thus, we conclude that the OXPHOS system in the plasma membrane may be required for the generation of extracellular ROS and the regulation of insulin signaling.

Keywords: Detergent-resistant lipid rafts; Extracellular superoxide; Insulin signaling; NADH; Plasma membrane oxidative phosphorylation.

MeSH terms

  • Animals
  • COS Cells
  • Catalase / metabolism
  • Catalase / pharmacology
  • Cell Line
  • Cell Line, Tumor
  • Cell Membrane / drug effects*
  • Cell Membrane / metabolism
  • Chlorocebus aethiops
  • Electron Transport Complex I / antagonists & inhibitors
  • Electron Transport Complex I / genetics
  • Electron Transport Complex I / metabolism
  • HEK293 Cells
  • Hep G2 Cells
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Humans
  • Insulin / metabolism
  • Insulin / pharmacology*
  • Membrane Microdomains / drug effects
  • Membrane Microdomains / metabolism
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Muscle Fibers, Skeletal / drug effects
  • Muscle Fibers, Skeletal / metabolism
  • NAD / metabolism
  • Oxidative Phosphorylation / drug effects*
  • Primary Cell Culture
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Signal Transduction
  • Superoxides / metabolism*

Substances

  • Insulin
  • RNA, Small Interfering
  • NAD
  • Superoxides
  • Catalase
  • Electron Transport Complex I
  • NDUFV1 protein, mouse