Hydrogel surfaces to promote attachment and spreading of endothelial progenitor cells
Article first published online: 6 JAN 2012
Copyright © 2012 John Wiley & Sons, Ltd.
Journal of Tissue Engineering and Regenerative Medicine
Volume 7, Issue 5, pages 337–347, May 2013
How to Cite
Camci-Unal, G., Nichol, J. W., Bae, H., Tekin, H., Bischoff, J. and Khademhosseini, A. (2013), Hydrogel surfaces to promote attachment and spreading of endothelial progenitor cells. J Tissue Eng Regen Med, 7: 337–347. doi: 10.1002/term.517
- Issue published online: 2 MAY 2013
- Article first published online: 6 JAN 2012
- Manuscript Accepted: 21 SEP 2011
- Manuscript Revised: 20 JUL 2011
- Manuscript Received: 29 MAR 2011
- hyaluronic acid;
- endothelial progenitor cells;
- cardiovascular implants
Endothelialization of artificial vascular grafts is a challenging process in cardiovascular tissue engineering. Functionalized biomaterials could be promising candidates to promote endothelialization in repair of cardiovascular injuries. The purpose of this study was to synthesize hyaluronic acid (HA) and heparin-based hydrogels that could promote adhesion and spreading of endothelial progenitor cells (EPCs). We report that the addition of heparin into HA-based hydrogels provides an attractive surface for EPCs promoting spreading and the formation of an endothelial monolayer on the hydrogel surface. To increase EPC adhesion and spreading, we covalently immobilized CD34 antibody (Ab) on HA–heparin hydrogels, using standard EDC/NHS amine-coupling strategies. We found that EPC adhesion and spreading on CD34 Ab-immobilized HA–heparin hydrogels was significantly higher than their non-modified analogues. Once adhered, EPCs spread and formed an endothelial layer on both non-modified and CD34 Ab-modified HA–heparin hydrogels after 3 days of culture. We did not observe significant adhesion and spreading when heparin was not included in the control hydrogels. In addition to EPCs, we also used human umbilical cord vein endothelial cells (HUVECs), which adhered and spread on HA–heparin hydrogels. Macrophages exhibited significantly less adhesion compared to EPCs on the same hydrogels. This composite material could possibly be used to develop surface coatings for artificial cardiovascular implants, due to its specificity for EPC and endothelial cells on an otherwise non-thrombogenic surface. Copyright © 2012 John Wiley & Sons, Ltd.