in vitro development of bioimplants made up of elastomeric scaffolds with peptide gel filling seeded with human subcutaneous adipose tissue-derived progenitor cells

• Published in: Journal of biomedical materials research. Part A 2015-11, Vol.103 (11), p.3419-3430
• Main Authors: Castells-Sala, Cristina, Martínez-Ramos, Cristina, Vallés-Lluch, Ana, Monleón Pradas, Manuel, Semino, Carlos
• Format: Article
• Language: English
• Subjects: Acrylic Resins - pharmacology; bioactive patch; Biocompatibility; Biocompatible Materials - pharmacology; Biomaterials; Biomedical materials; Cell Proliferation - drug effects; Cell Survival - drug effects; Cells, Cultured; Coating; elastomeric membrane; Gels - pharmacology; Gene Expression Profiling; Humans; mesenchymal stem cells-like cells; Microscopy, Confocal; Peptides; Peptides - pharmacology; Polymers - pharmacology; Prostheses and Implants; Scaffolds; self-assembling peptide; Stem Cells - cytology; Stem Cells - drug effects; Stem Cells - metabolism; Strategy; Subcutaneous Fat - cytology; Surgical implants; Tissue Scaffolds - chemistry
• ISSN: 1549-3296; 1552-4965
• DOI: 10.1002/jbm.a.35482

Myocardial tissue lacks the ability to regenerate itself significantly following a myocardial infarction. Thus, new strategies that could compensate this lack are of high interest. Cardiac tissue engineering (CTE) strategies are a relatively new approach that aims to compensate the tissue loss using combination of biomaterials, cells and bioactive molecules. The goal of the present study was to evaluate cell survival and growth, seeding capacity and cellular phenotype maintenance of subcutaneous adipose tissue‐derived progenitor cells in a new synthetic biomaterial scaffold platform. Specifically, here we tested the effect of the RAD16‐I peptide gel in microporous poly(ethyl acrylate) polymers using two‐dimensional PEA films as controls. Results showed optimal cell adhesion efficiency and growth in the polymers coated with the self‐assembling peptide RAD16‐I. Importantly, subATDPCs seeded into microporous PEA scaffolds coated with RAD16‐I maintained its phenotype and were able to migrate outwards the bioactive patch, hopefully toward the infarcted area once implanted. These data suggest that this bioimplant (scaffold/RAD16‐I/cells) can be suitable for further in vivo implantation with the aim to improve the function of affected tissue after myocardial infarction. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 3419–3430, 2015.