Injectable biomimetic liquid crystalline scaffolds enhance muscle stem cell transplantation
Author(s) -
Eduard Sleep,
Benjamin D. Cosgrove,
Mark McClendon,
Adam T. Preslar,
Charlotte H. Chen,
M. Hussain Sangji,
Charles M. Rubert Pérez,
Russell D. Haynes,
Thomas J. Meade,
Helen M. Blau,
Samuel I. Stupp
Publication year - 2017
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1708142114
Subject(s) - scaffold , regeneration (biology) , transplantation , stem cell , tissue engineering , nanofiber , microbiology and biotechnology , biomedical engineering , myocyte , regenerative medicine , in vivo , materials science , nanotechnology , biology , medicine , surgery
Muscle stem cells are a potent cell population dedicated to efficacious skeletal muscle regeneration, but their therapeutic utility is currently limited by mode of delivery. We developed a cell delivery strategy based on a supramolecular liquid crystal formed by peptide amphiphiles (PAs) that encapsulates cells and growth factors within a muscle-like unidirectionally ordered environment of nanofibers. The stiffness of the PA scaffolds, dependent on amino acid sequence, was found to determine the macroscopic degree of cell alignment templated by the nanofibers in vitro. Furthermore, these PA scaffolds support myogenic progenitor cell survival and proliferation and they can be optimized to induce cell differentiation and maturation. We engineered an in vivo delivery system to assemble scaffolds by injection of a PA solution that enabled coalignment of scaffold nanofibers with endogenous myofibers. These scaffolds locally retained growth factors, displayed degradation rates matching the time course of muscle tissue regeneration, and markedly enhanced the engraftment of muscle stem cells in injured and noninjured muscles in mice.
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