Use of bio-mimetic three-dimensional technology in therapeutics for heart disease

Bioengineered. 2014 May-Jun;5(3):193-7. doi: 10.4161/bioe.27751. Epub 2014 Jan 14.

Abstract

Due to the limited self-renewal capacity of cardiomyocytes, the mammalian heart exhibits impaired regeneration and insufficient ability to restore heart function after injury. Cardiovascular tissue engineering is currently considered as a promising alternative therapy to restore the structure and function of the failing heart. Recent evidence suggests that the epicardium may play critical roles in regulation of myocardial development and regeneration. One of the mechanisms that has been proposed for the restorative effect of the epicardium is the specific physiomechanical cues that this layer provides to the cardiac cells. In this article we explore whether a new generation of epicardium-mimicking, acellular matrices can be utilized to enhance cardiac healing after injury. The matrix consists of a dense collagen scaffold with optimized biomechanical properties approaching those of embryonic epicardium. Grafting the epicardial patch onto the ischemic myocardium--promptly after the incidence of infarct--resulted in preserved contractility, attenuated ventricular remodeling, diminished fibrosis, and vascularization within the injured tissue in the adult murine heart.

Keywords: angiogenesis; cardiac tissue engineering; cardiomyocyte; collagen; heart; myocardial infarction; scaffold.

MeSH terms

  • Animals
  • Biomimetic Materials
  • Cell Proliferation
  • Collagen / chemistry
  • Collagen / pharmacology*
  • Elastic Modulus
  • Embryo, Mammalian
  • Epithelial Cells / cytology
  • Epithelial Cells / physiology
  • Fibrosis / prevention & control
  • Gels
  • Implants, Experimental*
  • Male
  • Mice
  • Myocardial Contraction / drug effects
  • Myocardial Infarction / physiopathology
  • Myocardial Infarction / surgery
  • Myocardial Infarction / therapy*
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / physiology
  • Neovascularization, Physiologic / drug effects
  • Pericardium / cytology
  • Pericardium / physiology
  • Tissue Culture Techniques / methods*
  • Tissue Engineering / methods*
  • Ventricular Remodeling / drug effects

Substances

  • Gels
  • Collagen