Conditional HIF-1α expression produces a reversible cardiomyopathy

Raffi Bekeredjian, Chad B. Walton, Keith A. MacCannell, Jennifer Ecker, Fred Kruse, Joel T. Outten, David Sutcliffe, Robert D. Gerard, Richard K. Bruick, Ralph V. Shohet

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62 Scopus citations

Abstract

Background: The response to hypoxia in tissues is regulated by the heterodimeric transcription factor Hypoxia Inducible Factor-1 (HIF-1). Methodology/Principal Findings: We have created a strain of mice with inducible cardiomyocyte-specific expression of a mutated, oxygen-stable, form of HIF-1α. Cardiac function steadily decreased with transgene expression, but recovered after the transgene was turned off. Using long-oligo microarrays, we identified 162 transcripts more than 3-fold dysregulated in these hearts after transgene expression. Among the down-regulated genes the transcript for SERCA was reduced 46% and the protein 92%. This led us to an evaluation of calcium flux that showed diminished reuptake of cytoplasmic calcium in myocytes from these hearts, suggesting a mechanism for cardiac dysfunction. Conclusions/Significance: These results provide a deeper understanding of transcriptional activity of HIF in the heart, and show that enhanced HIF-1 activity is sufficient to cause contractile dysfunction in the adult heart. HIF is stabilized in the myocardium of patients with ischemic cardiomyopathy, and our results suggest that HIF could be contributing directly to the contractile dysfunction in this disease.

Original languageEnglish (US)
Article numbere11693
JournalPloS one
Volume5
Issue number7
DOIs
StatePublished - Aug 13 2010

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ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • General

Cite this

Bekeredjian, R., Walton, C. B., MacCannell, K. A., Ecker, J., Kruse, F., Outten, J. T., Sutcliffe, D., Gerard, R. D., Bruick, R. K., & Shohet, R. V. (2010). Conditional HIF-1α expression produces a reversible cardiomyopathy. PloS one, 5(7), [e11693]. https://doi.org/10.1371/journal.pone.0011693