Synthetic matrices to serve as niches for muscle cell transplantation

S Fernandes, S Kuklok, J McGonigle, H Reinecke… - Cells Tissues …, 2011 - karger.com
S Fernandes, S Kuklok, J McGonigle, H Reinecke, CE Murry
Cells Tissues Organs, 2011karger.com
Poor cell retention and limited cell survival after grafting are major limitations of cell therapy.
Recent studies showed that the use of matrices as vehicles at the time of cell injection can
significantly improve cell engraftment by providing an appropriate structure and physical
support for the injected cells. Properly designed matrices can also promote the organization
of the cells into a functioning cardiac-like tissue and enhance integration between the host
and the engrafted tissue. Furthermore, the use of an injectable biomaterial provides an …
Abstract
Poor cell retention and limited cell survival after grafting are major limitations of cell therapy. Recent studies showed that the use of matrices as vehicles at the time of cell injection can significantly improve cell engraftment by providing an appropriate structure and physical support for the injected cells. Properly designed matrices can also promote the organization of the cells into a functioning cardiac-like tissue and enhance integration between the host and the engrafted tissue. Furthermore, the use of an injectable biomaterial provides an opportunity to release in situ bioactive molecules that can further enhance the beneficial effects of cell transplantation. In this article we review a large variety of biologically derived synthetic and hybrid materials that have been tested as matrices for cardiac repair. We summarize the optimal parameters required for an ideal matrix including biocompatibility, injectability, degradation rate, and mechanical properties. Using an in vivo subcutaneous grafting model, we also provide novel data involving a side-by-side comparison of six synthetic matrices derived from maltodextrin. By systematically varying polymer molecular weight, cross-link density, and availability of cell adhesion motifs, a synthetic matrix was identified that supported skeletal myotube formation similar to Matrigel™. Our results emphasize not only the need to have a range of tunable matrices for cardiac cell therapy but also the importance of further characterizing the physical properties required for an ideal injectable matrix.
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