4.2 Article

Scaffold-Free Human Cardiac Tissue Patch Created from Embryonic Stem Cells

Journal

TISSUE ENGINEERING PART A
Volume 15, Issue 6, Pages 1211-1222

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ten.tea.2008.0151

Keywords

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Funding

  1. NIH [R24HL64387, P01 HL03174, R01 HL084642]
  2. NIGMS [P01GM081619]
  3. Bioengineering Cardiovascular Training Grant
  4. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R24HL064387, P01HL003174, R01HL084642, R01HL064387] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [T32EB001650] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [P01GM081619] Funding Source: NIH RePORTER

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Progress in cardiac tissue engineering has been limited by (1) unfavorable cell and host responses to biomaterial scaffolds, (2) lack of suitable human cardiomyocyte sources, and (3) lack of fabrication techniques for scalable production of engineered tissue constructs. Here we report a novel and scalable method to generate scaffold-free human cardiac tissue patches. Human embryonic stem cells were differentiated to cardiomyocytes using activin A and BMP4 and placed into suspension on a rotating orbital shaker. Cells aggregated to form macroscopic disc-shaped patches of beating tissue after 2 days. Patch diameter was directly proportional to input cell number (approximately 11 mm with 12 million cells), and patches were 300-600 mm thick. Cardiomyocytes were concentrated around the patch edges and exhibited increased purity and maturation with time, comprising approximately 80% of total cells after 11 days. Noncardiac cell elements, primarily epithelium, were present at day 2 but were diminished markedly at later time points. Cardiomyocyte proliferation occurred throughout the patches at day 2 but declined by day 8. Patches exhibited automaticity and synchronous calcium transients, indicating electromechanical coupling. These novel scaffold-free human myocardial patches address critical challenges related to human cell sourcing and tissue fabrication that previously inhibited progress in cardiac tissue engineering.

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