DocumentCode
2534322
Title
Micro-stamped ECM proteins enhance endothelial cell adhesion and directed growth
Author
Rubenstein, D.A. ; Frame, M.D.
Author_Institution
State Univ. of New York-Stony Brook, Stony Brook
fYear
2007
fDate
10-11 March 2007
Firstpage
183
Lastpage
184
Abstract
Our goal was to evaluate microvascular endothelial cell growth on hydrophilic glass surfaces micro-stamped with extracellular matrix proteins (ECM). A combination of photo-and soft-lithography was used to fabricate microstamps. We hypothesized that by day 3, human dermal microvascular endothelial cells (hDMECs) would have higher viability and density on the patterned matrices vs. on bare glass. Also, our preferential elongated morphology would be heightened on the stamped matrix. By day 3, we saw a four-fold increase in density on the stamped proteins. Viability was independent of the ECM type (fibronectin, laminin, collagen I and IV). Endothelial cell morphology was preferentially elongated on each ECM type, more so than on bare glass. This demonstrates the ability to concentrate the growth of endothelial cells within regions of microstamped ECM proteins.
Keywords
biochemistry; biomedical materials; cellular biophysics; molecular biophysics; photolithography; proteins; skin; soft lithography; tissue engineering; collagen I; collagen IV; endothelial cell adhesion; endothelial cell morphology; fibronectin; hDMEC; human dermal cell; hydrophilic glass surface; laminin; microstamped ECM proteins; microvascular endothelial cell growth; photolithography; soft-lithography; time 3 day; Adhesives; Bovine; Cells (biology); Dermis; Electrochemical machining; Extracellular; Glass; Humans; Morphology; Protein engineering;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioengineering Conference, 2007. NEBC '07. IEEE 33rd Annual Northeast
Conference_Location
Long Island, NY
Print_ISBN
978-1-4244-1033-0
Electronic_ISBN
978-1-4244-1033-0
Type
conf
DOI
10.1109/NEBC.2007.4413339
Filename
4413339
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