Prohibitin 1 modulates mitochondrial function of Stat3

Cell Signal. 2014 Oct;26(10):2086-95. doi: 10.1016/j.cellsig.2014.06.006. Epub 2014 Jun 26.

Abstract

Mitochondrial dysfunction in intestinal epithelial cells (IEC) is thought to precede the onset of inflammatory bowel diseases (IBD). Expression of Prohibitin 1 (PHB), a mitochondrial protein required for optimal electron transport chain (ETC) activity, is decreased in mucosal biopsies during active and inactive IBD. In addition to its activities as a transcription factor, Signal Transducer and Activator of Transcription 3 (Stat3) resides in the mitochondria of cells where phosphorylation at S727 is required for optimal ETC activity and protects against stress-induced mitochondrial dysfunction. Here, we show that PHB overexpression protects against mitochondrial stress and apoptosis of cultured IECs induced by TNFα, which is a pro-inflammatory cytokine involved in IBD pathogenesis. Expression of pS727-Stat3 dominant negative eliminates protection by PHB against TNFα-induced mitochondrial stress and apoptosis. PHB interacts with pS727-Stat3 in the mitochondria of cultured IECs and in colonic epithelium from wild-type mice. Our data suggest a protective role of PHB that is dependent on pS727-Stat3 to prevent mitochondrial dysfunction in IECs. Reduced levels of PHB during IBD may be an underlying factor promoting mitochondrial dysfunction of the intestinal epithelium.

Keywords: Electron transport chain; Intestinal epithelium; Mitochondria; Oxidative stress; Prohibitin; Stat3.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Caco-2 Cells
  • Cells, Cultured
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Humans
  • Intestinal Mucosa / cytology
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism*
  • Phosphorylation
  • Prohibitins
  • Protein Binding
  • Reactive Oxygen Species / metabolism
  • Repressor Proteins / chemistry
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • STAT3 Transcription Factor / chemistry
  • STAT3 Transcription Factor / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • PHB protein, human
  • Prohibitins
  • Reactive Oxygen Species
  • Repressor Proteins
  • STAT3 Transcription Factor
  • Tumor Necrosis Factor-alpha