Authors

Kao Li

Type

Text

Type

Thesis

Advisor

Rafailovich, Miriam | Sokolov, Jonathon | Pinkas-Sarafova, Adriana.

Date

2015-08-01

Keywords

Materials Science

Department

Department of Materials Science and Engineering.

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/76319

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

Cell migration is the critical process in the development and maintenance of multicellular organisms. It's a highly integrated multistep process that orchestrates a series of cellular behavior, such as embryonic development, wound healing and immune responses. A lot of effort has been dedicated to studying the basic principle and mechanism of cell movement since decades ago1-3. Cells can migrate in single cell or en masse fashion. We have already known that En masse cell migration is more related with physiological processes of tissue formation. And previous study has shown that cells would respond to different substrates, with various morphology or stiffness 4. Also, we believe there should be an evident and reasonable difference of migration fashions between young and aged cells as it should be. In this paper, we studied and demonstrated the migration of fluorescent human dermal fibroblast on PMMA flat thin film and fiber substrates on day 1,2,3,4 with en masse technique. We also applied P12, a fibronectin-derived cell survival peptide, on cells to see whether it could work in a positive way to promote cell migration as it did in enhancing cell survival in culture and improving wound healing in rat skin5. The results showed that cells move faster on aligned fibrous substrates than those on the planar thin film and the velocity on fiber would speed up as days went by. What's more exciting was that P12 accelerated cell migration on both kinds of substrates, which holds the potential to achieving fast wound healing. | 42 pages

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.