Synthetic MMP-13 degradable ECMs based on poly(N-isopropylacrylamide-co-acrylic acid) semi-interpenetrating polymer networks. I. Degradation and cell migration
✍ Scribed by Soyeon Kim; Eugene H. Chung; Michele Gilbert; Kevin E. Healy
- Book ID
- 102873385
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 923 KB
- Volume
- 75A
- Category
- Article
- ISSN
- 1549-3296
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✦ Synopsis
Abstract
Thermoresponsive and injectable semi‐interpenetrating polymer networks (sIPNs) containing a biospecific cell‐adhesive signal and proteolytically degradable domains were developed as a synthetic equivalent of the extracellular matrix (ECM). The sIPNs synthesized define a modular hydrogel ECM where different properties of the matrix can be manipulated independently, thus creating a system where parametric analysis of the effect of hydrogel properties on cell proliferation and differentiation is possible. sIPNs composed of poly(N‐isopropylacrylamide‐co‐acrylic acid) [p(NIPAAm‐co‐AAc)] and RGD‐grafted poly(acrylic acid) linear chains [p(AAc)‐g‐RGD] were synthesized with peptide crosslinkers containing a matrix metalloproteinase‐13 (MMP‐13, collagenase‐3) degradable domain. The lower critical solution temperature (LCST) of peptide‐crosslinked p(NIPAAm‐co‐AAc) sIPNs was not influenced by the addition of either linear p(AAc) or peptide‐modified p(AAc) chains (∼34°C) in PBS. Degradation of peptide‐crosslinked hydrogels and sIPNs was enzyme specific and concentration dependent. Exposure of rat calvarial osteoblast (RCO) culture to the degradation products from the peptide‐crosslinked hydrogels did not significantly affect cell viability. Migration of RCOs into the sIPNs was dependent upon the presence of both a cell‐adhesive RGD peptide (Ac‐CGGNGEPRGDTYRAY‐NH~2~) and proteolytically‐degradable crosslinks; however, there was greater dependence on the latter. The sIPNs synthesized are versatile materials for assessing cell fate in synthetic ECM constructs in vitro and tissue regeneration in vivo. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2005