Shear- vs. nanotopography-guided control of growth of endothelial cells on RGD-nanoparticle-nanowell arrays
Affiliation
Department of Agricultural and Biosystems Engineering, The University of Arizona, Tucson, AZ, 85721, USASarver Heart Center and Department of Medicine, College of Medicine, The University of Arizona, Tucson, AZ, 85721, USA
Department of Biomedical Engineering, The University of Arizona, Tucson, AZ, 85721, USA
Issue Date
2013
Metadata
Show full item recordPublisher
BioMed CentralCitation
McCracken et al. Journal of Biological Engineering 2013, 7:11 http://www.jbioleng.org/content/7/1/11Rights
© 2013 McCracken et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).Collection Information
This item is part of the UA Faculty Publications collection. For more information this item or other items in the UA Campus Repository, contact the University of Arizona Libraries at repository@u.library.arizona.edu.Abstract
Endothelialization of therapeutic cardiovascular implants is essential for their intravascular hemocompatibility. We previously described a novel nanowell-RGD-nanoparticle ensemble, which when applied to surfaces led to enhanced endothelialization and retention under static conditions and low flow rates. In the present study we extend our work to determine the interrelated effects of flow rate and the orientation of ensemble-decorated surface arrays on the growth, adhesion and morphology of endothelial cells. Human umbilical vascular endothelial cells (HUVECs) were grown on array surfaces with either 1 mum x 5 mum spacing ("parallel to flow") and 5 mum x 1 mum spacing ("perpendicular to flow") and were exposed to a range of shear stress of (0 to 4.7 +/- 0.2 dyn.cm-2 ), utilizing a pulsatile flow chamber. Under physiological flow (4.7 +/- 0.2 dyn.cm-2), RGD-nanoparticle-nanowell array patterning significantly enhanced cell adhesion and spreading compared with control surfaces and with static conditions. Furthermore, improved adhesion coincided with higher alignment to surface patterning, intimating the importance of interaction and response to the array surface as a means of resisting flow detachment. Under sub-physiological condition (1.7 +/- 0.3 dyn.cm-2corresponding to early angiogenesis), nanowell-nanoparticle patterning did not provide enhanced cell growth and adhesion compared with control surfaces. However, it revealed increased alignment along the direction of flow, rather than the direction of the pattern, thus potentially indicating a threshold for cell guidance and related retention. These results could provide a cue for controlling cell growth and alignment under varying physiological conditions.
EISSN
1754-1611Version
Final published versionAdditional Links
http://www.jbioleng.org/content/7/1/11ae974a485f413a2113503eed53cd6c53
10.1186/1754-1611-7-11
Scopus Count
Collections
Except where otherwise noted, this item's license is described as © 2013 McCracken et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).

