Assaying Mitochondrial Respiration as an Indicator of Cellular Metabolism and Fitness

Methods Mol Biol. 2017:1601:79-87. doi: 10.1007/978-1-4939-6960-9_7.

Abstract

Mitochondrial respiration is the most important generator of cellular energy under most circumstances. It is a process of energy conversion of substrates into ATP. The Seahorse equipment allows measuring oxygen consumption rate (OCR) in living cells and estimates key parameters of mitochondrial respiration in real-time mode. Through use of mitochondrial inhibitors, four key mitochondrial respiration parameters can be measured: basal, ATP production-linked, maximal, and proton leak-linked OCR. This approach requires application of mitochondrial inhibitors-oligomycin to block ATP synthase, FCCP-to make the inner mitochondrial membrane permeable for protons and allow maximum electron flux through the electron transport chain, and rotenone and antimycin A-to inhibit complexes I and III, respectively. This chapter describes the protocol of OCR assessment in the culture of primary myotubes obtained upon satellite cell fusion.

Keywords: Cell viability; Cellular respiration; Mitochondrial disease; Mitochondrial function; Myotubes; Satellite cells.

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Antimycin A / pharmacology
  • Biological Assay / instrumentation*
  • Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone / pharmacology
  • Cell Respiration
  • Cell Survival
  • Electron Transport Complex I / antagonists & inhibitors
  • Electron Transport Complex III / antagonists & inhibitors
  • Mice
  • Mitochondria / drug effects
  • Mitochondria / metabolism*
  • Muscle Fibers, Skeletal / drug effects
  • Muscle Fibers, Skeletal / metabolism
  • Oligomycins / pharmacology
  • Oxidative Phosphorylation*
  • Oxygen Consumption*
  • Primary Cell Culture
  • Proton Ionophores / pharmacology
  • Rotenone / pharmacology
  • Satellite Cells, Skeletal Muscle / drug effects
  • Satellite Cells, Skeletal Muscle / metabolism
  • Uncoupling Agents / pharmacology

Substances

  • Oligomycins
  • Proton Ionophores
  • Uncoupling Agents
  • Rotenone
  • Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
  • Antimycin A
  • Adenosine Triphosphate
  • Electron Transport Complex I
  • Electron Transport Complex III