Shear- vs. nanotopography-guided control of growth of endothelial cells on RGD-nanoparticle-nanowell arrays

Persistent Link:
http://hdl.handle.net/10150/610173
Title:
Shear- vs. nanotopography-guided control of growth of endothelial cells on RGD-nanoparticle-nanowell arrays
Author:
McCracken, Katherine; Tran, Phat; You, David; Slepian, Marvin; Yoon, Jeong-Yeol
Affiliation:
Department of Agricultural and Biosystems Engineering, The University of Arizona, Tucson, AZ, 85721, USA; Sarver 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
Publisher:
BioMed Central
Citation:
McCracken et al. Journal of Biological Engineering 2013, 7:11 http://www.jbioleng.org/content/7/1/11
Journal:
Journal of Biological Engineering
Rights:
© 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-2; corresponding 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:
1754-1611
DOI:
10.1186/1754-1611-7-11
Version:
Final published version
Additional Links:
http://www.jbioleng.org/content/7/1/11

Full metadata record

DC FieldValue Language
dc.contributor.authorMcCracken, Katherineen
dc.contributor.authorTran, Phaten
dc.contributor.authorYou, Daviden
dc.contributor.authorSlepian, Marvinen
dc.contributor.authorYoon, Jeong-Yeolen
dc.date.accessioned2016-05-20T09:00:17Z-
dc.date.available2016-05-20T09:00:17Z-
dc.date.issued2013en
dc.identifier.citationMcCracken et al. Journal of Biological Engineering 2013, 7:11 http://www.jbioleng.org/content/7/1/11en
dc.identifier.doi10.1186/1754-1611-7-11en
dc.identifier.urihttp://hdl.handle.net/10150/610173-
dc.description.abstractEndothelialization 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-2en
dc.description.abstractcorresponding 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.en
dc.language.isoenen
dc.publisherBioMed Centralen
dc.relation.urlhttp://www.jbioleng.org/content/7/1/11en
dc.rights© 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)en
dc.titleShear- vs. nanotopography-guided control of growth of endothelial cells on RGD-nanoparticle-nanowell arraysen
dc.typeArticleen
dc.identifier.eissn1754-1611en
dc.contributor.departmentDepartment of Agricultural and Biosystems Engineering, The University of Arizona, Tucson, AZ, 85721, USAen
dc.contributor.departmentSarver Heart Center and Department of Medicine, College of Medicine, The University of Arizona, Tucson, AZ, 85721, USAen
dc.contributor.departmentDepartment of Biomedical Engineering, The University of Arizona, Tucson, AZ, 85721, USAen
dc.identifier.journalJournal of Biological Engineeringen
dc.description.collectioninformationThis 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.en
dc.eprint.versionFinal published versionen
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