The use of new surface-modified poly(2-hydroxyethyl methacrylate) hydrogels in tissue engineering: treatment of the surface with fibronectin subunits versus Ac-CGGASIKVAVS-OH, cysteine, and 2-mercaptoethanol modification
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23946247
DOI
10.1002/jbm.a.34910
Knihovny.cz E-zdroje
- Klíčová slova
- 2-hydroxyethyl methacrylate, IKVAV (Ile-Lys-Val-Ala-Val) peptide, fibronectin, hydrogel, scaffold, tissue engineering,
- MeSH
- buněčná diferenciace MeSH
- cystein chemie MeSH
- fibronektiny chemie MeSH
- hydrogely * MeSH
- krysa rodu Rattus MeSH
- merkaptoethanol chemie MeSH
- mezenchymální kmenové buňky cytologie MeSH
- mikroskopie elektronová rastrovací MeSH
- peptidy chemie MeSH
- polyhydroxyethylmethakrylát chemie MeSH
- povrchové vlastnosti MeSH
- tkáňové inženýrství * MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cystein MeSH
- fibronektiny MeSH
- hydrogely * MeSH
- merkaptoethanol MeSH
- peptidy MeSH
- polyhydroxyethylmethakrylát MeSH
Superporous poly(2-hydroxyethyl methacrylate) is successfully used as a scaffold material for tissue engineering; however, it lacks functional groups that support cell adhesion. The objective of this study was to investigate the cell-adhesive properties of biomimetic ligands, such as laminin-derived Ac-CGGASIKVAVS-OH (SIKVAV) peptide and fibronectin subunits (Fn), as well as small molecules exemplified by 2-mercaptoethanol (ME) and cysteine (Cys), immobilized on a copolymer of 2-hydroxyethyl methacrylate (HEMA) with 2-aminoethyl methacrylate (AEMA) by a maleimide-thiol coupling reaction. The maleimide group was introduced to the P(HEMA-AEMA) hydrogels by the reaction of their amino groups with N-γ-maleimidobutyryl-oxysuccinimide ester (GMBS). Mesenchymal stem cells (MSCs) were used to investigate the cell adhesive properties of the modified hydrogels. A significantly larger area of cell growth as well as a higher cell density were found on Fn- and SIKVAV-modified hydrogels when compared to the ME- and Cys-modified supports or neat P(HEMA-AEMA). Moreover, Fn-modification strongly stimulated cell proliferation. The ability of MSCs to differentiate into adipocytes and osteoblasts was maintained on both Fn- and SIKVAV-modifications, but it was reduced on ME-modified hydrogels and neat P(HEMA-AEMA). The results show that the immobilization of SIKVAV and Fn-subunits onto superporous P(HEMA-AEMA) hydrogels via a GMBS coupling reaction improves cell adhesive properties. The high proliferative activity observed on Fn-modified hydrogels suggests that the immobilized Fn-subunits maintain their bioactivity and thus represent a promising tool for application in tissue engineering.
Citace poskytuje Crossref.org
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