4.8 Article

Epicardial application of cardiac progenitor cells in a 3D-printed gelatin/hyaluronic acid patch preserves cardiac function after myocardial infarction

Journal

BIOMATERIALS
Volume 61, Issue -, Pages 339-348

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2015.05.005

Keywords

Cardiac progenitor cells; Tissue printing; Cardiac tissue engineering; Cardiac regeneration; Heart failure

Funding

  1. BioMedical Materials Institute [P1.04 SMARTCARE]
  2. Dutch Ministry of Economic Affairs, Agriculture and Innovation
  3. Netherlands CardioVascular Research Initiative (CVON): the Dutch Heart Foundation
  4. Dutch Federation of University Medical Centers
  5. Netherlands Organization for Health Research and Development
  6. Royal Netherlands Academy of Sciences
  7. Dutch Heart Foundation
  8. Cenci Bolognetti-Pasteur Institute of Rome (IT)
  9. Leduq Foundation

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Cardiac cell therapy suffers from limitations related to poor engraftment and significant cell death after transplantation. In this regard, ex vivo tissue engineering is a tool that has been demonstrated to increase cell retention and survival. The aim of our study was to evaluate the therapeutic potential of a 3D-printed patch composed of human cardiac-derived progenitor cells (hCMPCs) in a hyaluronic acid/gelatin (HA/gel) based matrix. hCMPCs were printed in the HA/gel matrix (30 x 10(6) cells/ml) to form a biocomplex made of six perpendicularly printed layers with a surface of 2 x 2 cm and thickness of 400 um, in which they retained their viability, proliferation and differentiation capability. The printed biocomplex was transplanted in a mouse model of myocardial infarction (MI). The application of the patch led to a significant reduction in adverse remodeling and preservation of cardiac performance as was shown by both MRI and histology. Furthermore, the matrix supported the long-term in vivo survival and engraftment of hCMPCs, which exhibited a temporal increase in cardiac and vascular differentiation markers over the course of the 4 week follow-up period. Overall, we developed an effective and translational approach to enhance hCMPC delivery and action in the heart. (C) 2015 Elsevier Ltd. All rights reserved.

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