Integrin‐specific hydrogels functionalized with VEGF for vascularization and bone regeneration of critical‐size bone defects. Issue 4 (4th January 2016)
- Record Type:
- Journal Article
- Title:
- Integrin‐specific hydrogels functionalized with VEGF for vascularization and bone regeneration of critical‐size bone defects. Issue 4 (4th January 2016)
- Main Title:
- Integrin‐specific hydrogels functionalized with VEGF for vascularization and bone regeneration of critical‐size bone defects
- Authors:
- García, José R.
Clark, Amy Y.
García, Andrés J. - Abstract:
- Abstract: Vascularization of bone defects is considered a crucial component to the successful regeneration of large bone defects. Although vascular endothelial growth factor (VEGF) has been delivered to critical‐size bone defect models to augment blood vessel infiltration into the defect area, its potential to increase bone repair remains ambiguous. In this study, we investigated whether integrin‐specific biomaterials modulate the effects of VEGF on bone regeneration. We engineered protease‐degradable, VEGF‐loaded poly(ethylene glycol) (PEG) hydrogels functionalized with either a triple‐helical, α2 β1 integrin‐specific peptide GGYGGGP(GPP)5 GFOGER(GPP)5 GPC (GFOGER) or an αv β3 integrin‐targeting peptide GRGDSPC (RGD). Covalent incorporation of VEGF into the PEG hydrogel allowed for protease degradation‐dependent release of the protein while maintaining VEGF bioactivity. When applied to critical‐size segmental defects in the murine radius, GFOGER‐functionalized VEGF‐free hydrogels exhibited significantly increased vascular volume and density and resulted in a larger number of thicker blood vessels compared to RGD‐functionalized VEGF‐free hydrogels. VEGF‐loaded RGD hydrogels increased vascularization compared to VEGF‐free RGD hydrogels, but the levels of vascularization for these VEGF‐containing RGD hydrogels were similar to those of VEGF‐free GFOGER hydrogels. VEGF transiently increased bone regeneration in RGD hydrogels but had no effect at later time points. In GFOGERAbstract: Vascularization of bone defects is considered a crucial component to the successful regeneration of large bone defects. Although vascular endothelial growth factor (VEGF) has been delivered to critical‐size bone defect models to augment blood vessel infiltration into the defect area, its potential to increase bone repair remains ambiguous. In this study, we investigated whether integrin‐specific biomaterials modulate the effects of VEGF on bone regeneration. We engineered protease‐degradable, VEGF‐loaded poly(ethylene glycol) (PEG) hydrogels functionalized with either a triple‐helical, α2 β1 integrin‐specific peptide GGYGGGP(GPP)5 GFOGER(GPP)5 GPC (GFOGER) or an αv β3 integrin‐targeting peptide GRGDSPC (RGD). Covalent incorporation of VEGF into the PEG hydrogel allowed for protease degradation‐dependent release of the protein while maintaining VEGF bioactivity. When applied to critical‐size segmental defects in the murine radius, GFOGER‐functionalized VEGF‐free hydrogels exhibited significantly increased vascular volume and density and resulted in a larger number of thicker blood vessels compared to RGD‐functionalized VEGF‐free hydrogels. VEGF‐loaded RGD hydrogels increased vascularization compared to VEGF‐free RGD hydrogels, but the levels of vascularization for these VEGF‐containing RGD hydrogels were similar to those of VEGF‐free GFOGER hydrogels. VEGF transiently increased bone regeneration in RGD hydrogels but had no effect at later time points. In GFOGER hydrogels, VEGF did not show an effect on bone regeneration. However, VEGF‐free GFOGER hydrogels resulted in increased bone regeneration compared to VEGF‐free RGD hydrogels. These findings demonstrate the importance of integrin‐specificity in engineering constructs for vascularization and associated bone regeneration. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 104A: 889–900, 2016. … (more)
- Is Part Of:
- Journal of biomedical materials research. Volume 104:Issue 4(2016)
- Journal:
- Journal of biomedical materials research
- Issue:
- Volume 104:Issue 4(2016)
- Issue Display:
- Volume 104, Issue 4 (2016)
- Year:
- 2016
- Volume:
- 104
- Issue:
- 4
- Issue Sort Value:
- 2016-0104-0004-0000
- Page Start:
- 889
- Page End:
- 900
- Publication Date:
- 2016-01-04
- Subjects:
- vascularization -- cell adhesion -- mesenchymal stem cells
Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4965 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jbm.a.35626 ↗
- Languages:
- English
- ISSNs:
- 1549-3296
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.720000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
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