Modeling the Mitochondrial Cardiomyopathy of Barth Syndrome With Induced Pluripotent Stem Cell and Heart-On-Chip Technologies

Nat Med. 2014 Jun;20(6):616-23. doi: 10.1038/nm.3545. Epub 2014 May 11.

Abstract

Study of monogenic mitochondrial cardiomyopathies may yield insights into mitochondrial roles in cardiac development and disease. Here, we combined patient-derived and genetically engineered induced pluripotent stem cells (iPSCs) with tissue engineering to elucidate the pathophysiology underlying the cardiomyopathy of Barth syndrome (BTHS), a mitochondrial disorder caused by mutation of the gene encoding tafazzin (TAZ). Using BTHS iPSC-derived cardiomyocytes (iPSC-CMs), we defined metabolic, structural and functional abnormalities associated with TAZ mutation. BTHS iPSC-CMs assembled sparse and irregular sarcomeres, and engineered BTHS 'heart-on-chip' tissues contracted weakly. Gene replacement and genome editing demonstrated that TAZ mutation is necessary and sufficient for these phenotypes. Sarcomere assembly and myocardial contraction abnormalities occurred in the context of normal whole-cell ATP levels. Excess levels of reactive oxygen species mechanistically linked TAZ mutation to impaired cardiomyocyte function. Our study provides new insights into the pathogenesis of Barth syndrome, suggests new treatment strategies and advances iPSC-based in vitro modeling of cardiomyopathy.

Publication types

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

MeSH terms

  • Barth Syndrome / genetics
  • Barth Syndrome / physiopathology*
  • Cardiomyopathy, Dilated / genetics
  • Cardiomyopathy, Dilated / physiopathology*
  • Cell Separation
  • Humans
  • Induced Pluripotent Stem Cells / physiology*
  • Magnetics
  • Mitochondrial Diseases / genetics
  • Mitochondrial Diseases / physiopathology*
  • Models, Biological*
  • Myocardial Contraction / physiology
  • Myocytes, Cardiac / physiology
  • Reactive Oxygen Species / metabolism
  • Tissue Engineering / methods*
  • Transcription Factors / genetics*

Substances

  • Reactive Oxygen Species
  • TAZ protein, human
  • Transcription Factors