Research Proposal

From OpenWetWare

Revision as of 23:40, 5 May 2013 by Ebaa Al-Obeidi (Talk | contribs)
Jump to: navigation, search

Background

The cornea is the transparent, outermost part of the eye which protects the fragile intraocular contents from mechanical and pathogenic perturbations. It consists of three distinct layers: a tear-bathed, stratified layer of epithelial cells; a thick stroma of collagen fibrils embedded with quiescent fibroblasts; and an inner epithelial layer, called the endothelium. Poor cell growth in any one of these layers can result in a loss of corneal transparency and thus blindness. The endothelium in particular lacks a robust proliferative response to cell loss, and this can hinder recovery after eye surgery and in diseases such as keratoconus, which affects between 1 in 500 and 1 in 2000 people in the U.S. <issue of endothelial to mesenchymal (fibroblast?) transfer>.

Project Idea

Our goal is to determine whether we can enhance the proliferation of human corneal endothelial cells (HCECs) while maintaining their phenotype. We will use ROCK inhibitor to increase the proliferation of HCECs and study whether the presence of TGF-Beta will allow the cells to maintain their phenotype in culture.

References

Okumura, Naoki, EunDuck Kay, et al. "Inhibition of TGF-β Signaling Enables Human Corneal Endothelial Cell Expansion In Vitro for Use in Regenerative Medicine." PLoS One. 8.2 (2013): n. page. Web. 5 May. 2013. <http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581499/>.

This paper demonstrated that the use of SB431542, a selective inhibitor of the TGF-β receptor, in culture media counteracted the development of fibroblastic phenotypes in HCECs.

Pipparelli, Aurélien, Yvan Arsenijevic, et al. "ROCK Inhibitor Enhances Adhesion and Wound Healing of Human Corneal Endothelial Cells." PLoS One. 8.4 (2013): n. page. Web. 5 May. 2013. <http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633902/>.

This paper...

Personal tools