Regulation of heat shock protein 60 and 72 expression in the failing heart

J Mol Cell Cardiol. 2010 Feb;48(2):360-6. doi: 10.1016/j.yjmcc.2009.11.009. Epub 2009 Nov 27.


Heart failure, a progressive, fatal disease of the heart muscle, is a state of chronic inflammation and injury. Heat shock protein (HSP) 72, a ubiquitous protective protein that is well-established as cardioprotective, is not increased in heart failure. In contrast, HSP60 levels are doubled in the failing heart. We hypothesized that HSF-1 is not activated in heart failure and that the increased expression of HSP60 was driven by NFkappaB activation. To test this hypothesis, we measured levels of heat shock factor (HSF) -1 and -2, the transcription factors controlling HSP expression, which were increased in heart failure. There was no increased phosphorylation of serine 230 or serine 303/307 in HSF-1, which are thought to regulate its activity; EMSA showed no increase in HSF binding activity with heart failure. Nonetheless, mRNA was increased for HSP60, but not HSP72. In contrast to HSF, NFkappaB activity was increased in heart failure. HSP60, but not HSP72, contained NFkappaB binding elements. ChIP assay demonstrated increased binding of NFkappaB to both of the NFkappaB binding elements in the heart failure HSP60 gene. TNFalpha treatment was used to test the role of NFkappaB activation in HSP60 expression in a cardiac cell line. TNFalpha increased HSP60 expression, and this could be prevented by pretreatment with siRNA inhibiting p65 expression. In conclusion, HSP72 is not increased in heart failure because HSF activity is not changed; increased expression of HSP60 may be driven by NFkappaB activation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Binding Sites
  • Blotting, Western
  • Chaperonin 60 / genetics*
  • Chaperonin 60 / metabolism
  • Chromatin Immunoprecipitation
  • DNA-Binding Proteins / metabolism
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation*
  • HSP72 Heat-Shock Proteins / genetics*
  • HSP72 Heat-Shock Proteins / metabolism
  • Heart Failure / genetics*
  • Heart Failure / physiopathology
  • Heart Function Tests
  • Heat Shock Transcription Factors
  • NF-kappa B / metabolism
  • Phosphorylation
  • Phosphoserine / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Transcription Factors / metabolism


  • Chaperonin 60
  • DNA-Binding Proteins
  • HSP72 Heat-Shock Proteins
  • Heat Shock Transcription Factors
  • NF-kappa B
  • Transcription Factors
  • Phosphoserine