Engineered heart tissue grafts improve systolic and diastolic function in infarcted rat hearts.

  • Wolfram-Hubertus Zimmermann
  • Ivan Melnychenko
  • Gerald Wasmeier
  • Michael Didié
  • Hiroshi Naito
  • Uwe Nixdorff
  • Andreas Hess
  • Lubos Budinsky
  • Kay Brune
  • Bjela Michaelis
  • Stefan Dhein
  • Alexander Schwoerer
  • Heimo Ehmke
  • Thomas Eschenhagen

Abstract

The concept of regenerating diseased myocardium by implantation of tissue-engineered heart muscle is intriguing, but convincing evidence is lacking that heart tissues can be generated at a size and with contractile properties that would lend considerable support to failing hearts. Here we created large (thickness/diameter, 1-4 mm/15 mm), force-generating engineered heart tissue from neonatal rat heart cells. Engineered heart tissue formed thick cardiac muscle layers when implanted on myocardial infarcts in immune-suppressed rats. When evaluated 28 d later, engineered heart tissue showed undelayed electrical coupling to the native myocardium without evidence of arrhythmia induction. Moreover, engineered heart tissue prevented further dilation, induced systolic wall thickening of infarcted myocardial segments and improved fractional area shortening of infarcted hearts compared to controls (sham operation and noncontractile constructs). Thus, our study provides evidence that large contractile cardiac tissue grafts can be constructed in vitro, can survive after implantation and can support contractile function of infarcted hearts.

Bibliographical data

Original languageGerman
Article number4
ISSN1078-8956
Publication statusPublished - 2006
pubmed 16582915