TNF-α mediates mitochondrial uncoupling and enhances ROS-dependent cell migration via NF-κB activation in liver cells

FEBS Lett. 2014 Jan 3;588(1):175-83. doi: 10.1016/j.febslet.2013.11.033. Epub 2013 Dec 4.

Abstract

Development of hepatocellular carcinoma (HCC) is accompanied by a continuous increase in reactive oxygen species (ROS) levels. To investigate the primary source of ROS in liver cells, we used tumor necrosis factor-alpha (TNF-α) as stimulus. Applying inhibitors against the respiratory chain complexes, we identified mitochondria as primary source of ROS production. TNF-α altered mitochondrial integrity by mimicking a mild uncoupling effect in liver cells, as indicated by a 40% reduction in membrane potential and ATP depletion (35%). TNF-α-induced ROS production activated NF-κB 3.5-fold and subsequently enhanced migration up to 12.7-fold. This study identifies complex I and complex III of the mitochondrial respiratory chain as point of release of ROS upon TNF-α stimulation of liver cells, which enhances cell migration by activating NF-κB signalling.

Keywords: CCCP; H(2)DCF-DA; HBV; HCV; Hepatocellular carcinoma (HCC); Hepatocytes; Liver cancer; Mitochondria; N-acetylcysteine; NAC; NF-κB; ROS; Reactive oxygen species (ROS); TMRE; TNF-α; carbonyl cyanide m-chlorophenyl hydrazine; dichlorofluorescein diacetate; hepatitis B virus; hepatitis C virus; reactive oxygen species; tetramethylrhodamine ethyl ester; tumor necrosis factor-alpha.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATPases Associated with Diverse Cellular Activities
  • Animals
  • Antimycin A / pharmacology
  • Blotting, Western
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology
  • Cell Line, Tumor
  • Cell Movement / drug effects*
  • Cells, Cultured
  • Electron Transport Complex III / genetics
  • Electron Transport Complex III / metabolism
  • Gene Expression / drug effects
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Humans
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology
  • Membrane Potential, Mitochondrial / drug effects
  • Mice
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Mitochondria / physiology
  • NADH Dehydrogenase / genetics
  • NADH Dehydrogenase / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Polymerase Chain Reaction
  • RNA Interference
  • RNA-Directed DNA Polymerase
  • Reactive Oxygen Species / metabolism*
  • Rotenone / pharmacology
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Uncoupling Agents / pharmacology

Substances

  • BCS1L protein, human
  • NF-kappa B
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Uncoupling Agents
  • Rotenone
  • Antimycin A
  • NADH Dehydrogenase
  • RNA-Directed DNA Polymerase
  • ATPases Associated with Diverse Cellular Activities
  • NDUFAF1 protein, human
  • Electron Transport Complex III