A redox-dependent pathway for regulating class II HDACs and cardiac hypertrophy

Cell. 2008 Jun 13;133(6):978-93. doi: 10.1016/j.cell.2008.04.041.

Abstract

Thioredoxin 1 (Trx1) facilitates the reduction of signaling molecules and transcription factors by cysteine thiol-disulfide exchange, thereby regulating cell growth and death. Here we studied the molecular mechanism by which Trx1 attenuates cardiac hypertrophy. Trx1 upregulates DnaJb5, a heat shock protein 40, and forms a multiple-protein complex with DnaJb5 and class II histone deacetylases (HDACs), master negative regulators of cardiac hypertrophy. Both Cys-274/Cys-276 in DnaJb5 and Cys-667/Cys-669 in HDAC4 are oxidized and form intramolecular disulfide bonds in response to reactive oxygen species (ROS)-generating hypertrophic stimuli, such as phenylephrine, whereas they are reduced by Trx1. Whereas reduction of Cys-274/Cys-276 in DnaJb5 is essential for interaction between DnaJb5 and HDAC4, reduction of Cys-667/Cys-669 in HDAC4 inhibits its nuclear export, independently of its phosphorylation status. Our study reveals a novel regulatory mechanism of cardiac hypertrophy through which the nucleocytoplasmic shuttling of class II HDACs is modulated by their redox modification in a Trx1-sensitive manner.

Publication types

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

MeSH terms

  • Active Transport, Cell Nucleus
  • Amino Acid Sequence
  • Animals
  • COS Cells
  • Cardiomegaly / metabolism*
  • Cell Nucleus / metabolism
  • Chlorocebus aethiops
  • Cysteine / metabolism
  • HSP40 Heat-Shock Proteins / metabolism
  • Histone Deacetylases / chemistry
  • Histone Deacetylases / metabolism*
  • Mice
  • Molecular Sequence Data
  • Myocytes, Cardiac / metabolism
  • Oxidation-Reduction*
  • Phosphorylation
  • Sequence Alignment
  • Signal Transduction*
  • Thioredoxins / metabolism

Substances

  • Dnajb5 protein, mouse
  • HSP40 Heat-Shock Proteins
  • Txn1 protein, mouse
  • Thioredoxins
  • Hdac5 protein, mouse
  • Histone Deacetylases
  • Cysteine