4.8 Article

The influence of heart valve leaflet matrix characteristics on the interaction between human mesenchymal stem cells and decellularized scaffolds

Journal

BIOMATERIALS
Volume 30, Issue 25, Pages 4104-4116

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2009.04.031

Keywords

Heart valve; Heart valve tissue engineering; Mesenchymal stem cells; Cell-ECM interactions

Funding

  1. Azione Biotech II
  2. Biomedical Foundation for Cardiovascular Research (FoRiBiCa)
  3. Italian Ministry of the University and Scientific Research
  4. European Community Consortium Agreement [IP 018630]
  5. Fondazione Citta della Speranza
  6. Great Ormond Street Hospital Childrens Charity [V1230] Funding Source: researchfish

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The potential for in vitro colonization of decellularized valves by human bone marrow mesenchymal stem cells (hBM-MSCs) towards the anisotropic layers ventricularis and fibrosa and in homo- vs. heterotypic cell-ECM interactions has never been investigated. hBM-MSCs were expanded and characterized by immunofluorescence and FACS analysis. Porcine and human pulmonary valve leaflets (p- and hPVLs, respectively) underwent decellularization with Triton X100-sodium cholate treatment (TRICOL), followed by nuclear fragment removal. hBM-MSCs (2 x 10(6) cells/cm(2)) were seeded onto fibrosa (FS) or ventricularis (VS) of decellularized PVLs, precoated with FBS and fibronectin, and statically cultured for 30 days. Bioengineered PVLs revealed no histopathological features but a reconstructed endothelium lining and the presence of fibroblasts, myofibroblasts and SMCs, as in the corresponding native leaflet. The two valve layers behaved differently as regards hBM-MSC repopulation potential, however, with a higher degree of 3D spreading and differentiation in VS than in FS samples, and with enhanced cell survival and colonization effects in the homotypic ventricularis matrix, suggesting that hBM-MSC phenotypic conversion is strongly influenced in vitro by the anisotropic valve microstructure and species-specific matching between extracellular matrix and donor cells. These findings are of particular relevance to in vivo future applications of valve tissue engineering. (C) 2009 Elsevier Ltd. All rights reserved.

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