Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-27T01:42:39.766Z Has data issue: false hasContentIssue false

Effect of Nano-to Micro-Scale Surface Topography on the Orientation of Endothelial Cells

Published online by Cambridge University Press:  01 February 2011

P. Uttayarat
Affiliation:
Materials Science and Engineering Department, University of Pennsylvania, Philadelphia, PA 19104, U.S.A.
Peter I. Lelkes
Affiliation:
School of Biomedical Engineering, Science and Health Systems, Drexel University Philadelphia, PA 19104, U.S.A.
Russell J. Composto
Affiliation:
Materials Science and Engineering Department, University of Pennsylvania, Philadelphia, PA 19104, U.S.A.
Get access

Abstract

The effect of grating textures on the alignment of cell shape and intracellular actin cytoskeleton has been investigated in bovine aortic endothelial cells (BAECs) cultured on a model cross-linked poly(dimethylsiloxane) (PDMS). Grating-textured PDMS substrates, having a variation in channel depths of 200 nm, 500 nm, 1 μm and 5 μm, were coated with fibronectin (Fn) to promote endothelial cell adhesion and cell orientation. As cells adhered to the Fn-coated surface, the underlying grating texture has shown to direct the alignment of cell shape, F-actin and focal contacts parallel to the channels. Cell alignment was observed to increase with increasing channel depths, reaching the maximum orientation where most cells aligned parallel to channels on 1-μm textured surface. Immunofluorescence studies showed that F-actin stress fibers and vinculin at focal contacts also aligned parallel to the channels. Cell proliferation was found to be independent of grating textures and the alignment of cell shape was maintained at confluence.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Lamba, N. M. K. and Cooper, S. L., in Tissue engineering of vascular prosthetic grafts, edited by Zilla, P. and Greisler, H. P., (Landes Bioscience, 2004). pp. 553559.Google Scholar
2. Chen, C. S., Mrksich, M., Huang, S., Whitesides, G. M., and Ingber, D. E., Scinece 276, 1425 (1997).Google Scholar
3. Mathur, A. B., Chan, B. P., Truskey, G. A., and Reichert, W. M., J Biomed Mater Res Part A 66A, 729 (2003).Google Scholar
4. van Kooten, T. G. and von Recum, A. F., Tissue Engineering 5, 223 (1999).Google Scholar
5. Cook, A. D., Hrkach, J. S., Gao, N. N., Johnson, I. M., Pajvani, U. B., Cannizzaro, S. M., and Langer, R., J Biomed Mater Res 35, 513 (1997).Google Scholar
6. Murugesan, G., Ruegsegger, M. A., Kligman, F., Marchant, R. E., and Kottke-Marchant, K., Cell Comm and Adh 9, 59 (2002).Google Scholar
7. Sidouni, F.-Z., Nurdin, N., Chabrecek, P., Lohmann, D., Vogt, J., Xanthopoulos, N., Mathieu, H. J., Francois, P., Vaudaux, P., and Descouts, P., Surface Science 491, 355 (2001).Google Scholar
8. Jiang, X., Takayama, S., Qian, X., Ostuni, E., Wu, H., Bowden, N., LeDuc, P., Ingber, D., and Whitesides, G. M., Langmuir 18, 3273 (2002).Google Scholar
9. Nerem, R. M., J Biomech Eng 103, 172 (1981).Google Scholar
10. García, A. J., Vega, M. D., and Boettiger, D., Mol Biol Cell 10, 785 (1999).Google Scholar
11. Toworfe, G. K., Composto, R. J., Adams, C. S., Shapiro, I. M., and Ducheyne, P., J Biomed Mater Res 71A, 449 (2004).Google Scholar
12. Uttayarat, P., Toworfe, G., Lelkes, P. I., and Composto, R. J., J. Biomed Mater Res (2004).Google Scholar