An electrically coupled tissue-engineered cardiomyocyte scaffold improves cardiac function in rats with chronic heart failure

J Heart Lung Transplant. 2014 Apr;33(4):438-45. doi: 10.1016/j.healun.2013.12.004. Epub 2013 Dec 17.


Background: Varying strategies are currently being evaluated to develop tissue-engineered constructs for the treatment of ischemic heart disease. This study examines an angiogenic and biodegradable cardiac construct seeded with neonatal cardiomyocytes for the treatment of chronic heart failure (CHF).

Methods: We evaluated a neonatal cardiomyocyte (NCM)-seeded 3-dimensional fibroblast construct (3DFC) in vitro for the presence of functional gap junctions and the potential of the NCM-3DFC to restore left ventricular (LV) function in an in vivo rat model of CHF at 3 weeks after permanent left coronary artery ligation.

Results: The NCM-3DFC demonstrated extensive cell-to-cell connectivity after dye injection. At 5 days in culture, the patch contracted spontaneously in a rhythmic and directional fashion at 43 ± 3 beats/min, with a mean displacement of 1.3 ± 0.3 mm and contraction velocity of 0.8 ± 0.2 mm/sec. The seeded patch could be electrically paced at nearly physiologic rates (270 ± 30 beats/min) while maintaining coordinated, directional contractions. Three weeks after implantation, the NCM-3DFC improved LV function by increasing (p < 0.05) ejection fraction 26%, cardiac index 33%, dP/dt(+) 25%, dP/dt(-) 23%, and peak developed pressure 30%, while decreasing (p < 0.05) LV end diastolic pressure 38% and the time constant of relaxation (Tau) 16%. At 18 weeks after implantation, the NCM-3DFC improved LV function by increasing (p < 0.05) ejection fraction 54%, mean arterial pressure 20%, dP/dt(+) 16%, dP/dt(-) 34%, and peak developed pressure 39%.

Conclusions: This study demonstrates that a multicellular, electromechanically organized cardiomyocyte scaffold, constructed in vitro by seeding NCM onto 3DFC, can improve LV function long-term when implanted in rats with CHF.

Keywords: cardiomyocytes; cell therapy; chronic heart failure; ejection fraction; ventricles; ventricular function.

Publication types

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

MeSH terms

  • Animals
  • Cardiac Pacing, Artificial*
  • Cell Communication / physiology
  • Cell Differentiation / physiology
  • Disease Models, Animal
  • Echocardiography
  • Heart Failure / pathology
  • Heart Failure / physiopathology*
  • Heart Failure / therapy*
  • Hemodynamics / physiology
  • Myocardial Ischemia / pathology
  • Myocardial Ischemia / physiopathology*
  • Myocardial Ischemia / therapy*
  • Myocytes, Cardiac / pathology
  • Myocytes, Cardiac / transplantation*
  • Neovascularization, Physiologic / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Stroke Volume / physiology
  • Tissue Engineering / methods*
  • Tissue Scaffolds*
  • Ventricular Function, Left / physiology*