Production of heparin-containing hydrogels for modulating cell responses

TitleProduction of heparin-containing hydrogels for modulating cell responses
Publication TypeJournal Article
Year of Publication2009
AuthorsNie, T., Akins R. E., & Kiick K. L.
JournalActa biomaterialia
Volume5
Issue3
Pagination865-75
Date Published2009 Mar
ISSN1878-7568
KeywordsAmino Acid Sequence; Aorta; Biocompatible Materials; Bisbenzimidazole; Cell Adhesion; Cells, Cultured; Elastic Modulus; Fibroblasts; Fluorescent Dyes; Heparin, Low-Molecular-Weight; Humans; Hydrogels; Ligands; Maleimides; Molecular Weight; Polyethylene Glycols; Rheology
Abstract

Successful tissue regeneration requires that biomaterials have optimal bioactivity and mechanical properties. Heparin-containing hydrogels that can be crosslinked in situ were designed to contain tunable amounts of biological components (e.g. heparin, arginine-glycine-aspartate (RGD)) as well as to exhibit controlled mechanical properties (e.g. shear modulus). These gel parameters can also be tuned to provide controlled delivery of proteins, such as growth factors, for regulating cellular behavior. Maleimide-functionalized low-molecular-weight heparin (LWMH) was conjugated to a poly(ethylene glycol) (PEG) hydrogel. The elastic shear modulus, as assessed via oscillatory rheology experiments, could be tuned by the concentration of polymer in the hydrogel, and by the end group functionality of PEG. Hydrogels of two different moduli (2.8 and 0.4kPa) were used to study differences in the response of human aortic adventitial fibroblasts (AoAF) in two-dimensional cell culture experiments. These experiments indicated that the AoAFs show improved adhesion to materials with the higher modulus. Evaluation of cell responses to hydrogels with RGD linked to the hydrogels via conjugation to PEG or to LMWH indicated improved cellular responses to these materials when the bioactive ligands were chemically attached through linkage to the PEG rather than to the LMWH. These results highlight important design considerations in the tailoring of these materials for cardiovascular tissue engineering applications.

DOI10.1016/j.actbio.2008.12.004
Alternate JournalActa Biomater
Refereed DesignationRefereed