Currently there are no effective treatments for stimulating healing of stromal endothelial wounds caused by surgery, trauma or disease, yet inadequate healing of corneal wounds can lead to severe complications. Our long term goals are to understand the molecular mechanisms that regulate the natural healing process in the cornea, and to develop ways to stimulate corneal healing. Our hypothesis is that normal healing in the cornea is regulated by peptide growth factors produced by cells in the area of injury. These peptide growth factors operate via autocrine or paracrine mechanisms to stimulate mitosis and migration of corneal cells. This hypothesis implies that inadequate corneal healing results from insufficient production of wound stimulating factors and their receptors or the overproduction of wound inhibiting factors and their receptors. Also, it implies that addition of appropriate stimulating peptide growth factors would stimulate healing of corneal wounds. To test this hypothesis, we propose to analyze bovine and human corneal keratocytes and endothelial cells for production of mRNA for eight different growth factors (EGF, bFGF, aFGF, TGF-alpha, TGF-beta, IGF-I, IGF-II, PDGF) using cDNA hybridization techniques (dot-blot, Northern, in situ hybridization). We will determine if the levels of these growth factors and the EGF receptor change during the course of wound healing, and we will investigate what physiological substances may regulate the level of their expression. Also, we will investigate the molecular mechanism of EGF action on corneal cells by biochemically characterizing the cellular substrates which are phosphorylated by the EGF receptor kinase. To further test this hypothesis in vivo, we will measure the strength of corneal incisions in rabbits treated topically with biosynthetic bFGF, IGF- I, PDGF, or TGF-beta, and we will evaluate the effect of formulations containing growth factors on stimulating mitosis of cat corneal endothelium. Results from these experiments should further our basic understanding of the molecular mechanism regulating corneal wound healing, and indicate the potential clinical usefulness of exogenous growth factor therapy in stimulating corneal healing.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005587-07
Application #
3260745
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1989-01-01
Project End
1992-06-30
Budget Start
1990-07-01
Budget End
1992-06-30
Support Year
7
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Florida
Department
Type
Schools of Medicine
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Feng, Xiaodi; Pi, Liya; Sriram, Sriniwas et al. (2017) Connective tissue growth factor is not necessary for haze formation in excimer laser wounded mouse corneas. PLoS One 12:e0172304
Pi, Liya; Chung, Pei-Yu; Sriram, Sriniwas et al. (2015) Connective tissue growth factor differentially binds to members of the cystine knot superfamily and potentiates platelet-derived growth factor-B signaling in rabbit corneal fibroblast cells. World J Biol Chem 6:379-88
Pi, Liya; Jorgensen, Marda; Oh, Seh-Hoon et al. (2015) A disintegrin and metalloprotease with thrombospondin type I motif 7: a new protease for connective tissue growth factor in hepatic progenitor/oval cell niche. Am J Pathol 185:1552-63
Pi, Liya; Robinson, Paulette M; Jorgensen, Marda et al. (2015) Connective tissue growth factor and integrin ?v?6: a new pair of regulators critical for ductular reaction and biliary fibrosis in mice. Hepatology 61:678-91
Sriram, Sriniwas; Gibson, Daniel J; Robinson, Paulette et al. (2014) Assessment of anti-scarring therapies in ex vivo organ cultured rabbit corneas. Exp Eye Res 125:173-82
Gibson, Daniel J; Pi, Liya; Sriram, Sriniwas et al. (2014) Conditional knockout of CTGF affects corneal wound healing. Invest Ophthalmol Vis Sci 55:2062-70
Gibson, Daniel J; Tuli, Sonal S; Schultz, Gregory S (2013) The progression of haze formation in rabbit corneas following phototherapeutic keratectomy. Invest Ophthalmol Vis Sci 54:4776-81
Pi, Liya; Shenoy, Anitha K; Liu, Jianwen et al. (2012) CCN2/CTGF regulates neovessel formation via targeting structurally conserved cystine knot motifs in multiple angiogenic regulators. FASEB J 26:3365-79
Blalock, Timothy D; Gibson, Daniel J; Duncan, Matthew R et al. (2012) A connective tissue growth factor signaling receptor in corneal fibroblasts. Invest Ophthalmol Vis Sci 53:3387-94
Tandon, Ashish; Tovey, Jonathan C K; Waggoner, Michael R et al. (2012) Vorinostat: a potent agent to prevent and treat laser-induced corneal haze. J Refract Surg 28:285-90

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