Proper wound repair following injury, surgery, and disease is essential to maintaining a clear cornea and ultimately preserving vision. The long-term goal of this project is to understand the mechanisms involved in corneal wound repair. Two intriguing aspects of corneal wound repair are that the wound response varies dramatically between the wound area and the area adjacent to the wound, and that the type of wound affects both the epithelial and stromal healing responses. Our previous data suggest that transforming growth factor beta (TGF-?) plays a critical role in the regulation of corneal wound repair. As part of our studies, we have found that the integrin aV?6 is specifically upregulated in the wounded epithelium, and that thrombospondin- 1 (TSP-1) is upregulated in the stromal cells subjacent to the wound area. Both aV?6 and TSP-1 activate TGF-?, which is normally present in an inactive latent form. The hypothesis that we propose to test is that corneal wounding stimulates the upregulation of aV?6 in the epithelium and TSP-1 in the stromal cells leading to the local activation of TGF-?, resulting in inhibition of proliferation in the migrating epithelium and stimulation of proliferation and migration of the fibroblasts in the subjacent stroma. We propose three specific aims to examine the following questions: First, what is the effect of the total lack of TGF-? signaling on wound healing? Second, what is the effect of altered TGF-? activation through aV?6 on the epithelium after wounding? Third, what is the effect of altered TGF-? activation through TSP-1 in the stroma after wounding? In vivo and in vitro wound healing models of rats and mice will be used to examine these questions. Wound healing in mice lacking components of the TGF-? signaling pathway, aV?6 and TSP-1 will be examined to determine the function of these proteins in wound repair. In addition, specific inhibitors of TGF-? signaling, aV?6 and TSP-1 will be examined to determine their role in corneal wound repair. Wound healing processes to be examined include: cell proliferation, cell migration, basement membrane resynthesis, and myofibroblast generation. Relevance to public health - Wound repair is a basic and crucial property of all tissues including the cornea. Because of its exposed position at the surface of the eye, the cornea is at risk to a variety of wounds including those created during laser surgery to correct vision. Our studies will allow a comparison of wounds that heal with minimal complications vs. wounds that heal in a manner that can be vision threatening.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005665-25
Application #
7663054
Study Section
Special Emphasis Panel (ZRG1-BDCN-F (02))
Program Officer
Shen, Grace L
Project Start
1984-12-01
Project End
2012-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
25
Fiscal Year
2009
Total Cost
$567,140
Indirect Cost
Name
Schepens Eye Research Institute
Department
Type
DUNS #
073826000
City
Boston
State
MA
Country
United States
Zip Code
02114
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Han, Kyu-Yeon; Tran, Jennifer A; Chang, Jin-Hong et al. (2017) Potential role of corneal epithelial cell-derived exosomes in corneal wound healing and neovascularization. Sci Rep 7:40548
Sriram, Sriniwas; Tran, Jennifer A; Guo, Xiaoqing et al. (2017) PDGFR? Is a Key Regulator of T1 and T3's Differential Effect on SMA Expression in Human Corneal Fibroblasts. Invest Ophthalmol Vis Sci 58:1179-1186
Guo, Xiaoqing; Hutcheon, Audrey E K; Tran, Jennifer A et al. (2017) TGF-?-target genes are differentially regulated in corneal epithelial cells and fibroblasts. New Front Ophthalmol 3:
Sriram, Sriniwas; Tran, Jennifer A; Guo, Xiaoqing et al. (2017) Development of wound healing models to study TGF?3's effect on SMA. Exp Eye Res 161:52-60
Zareian, Ramin; Susilo, Monica E; Paten, Jeffrey A et al. (2016) Human Corneal Fibroblast Pattern Evolution and Matrix Synthesis on Mechanically Biased Substrates. Tissue Eng Part A 22:1204-1217
Guo, Xiaoqing; Hutcheon, Audrey E K; Zieske, James D (2016) Molecular insights on the effect of TGF-?1/-?3 in human corneal fibroblasts. Exp Eye Res 146:233-41
Pal-Ghosh, Sonali; Pajoohesh-Ganji, Ahdeah; Tadvalkar, Gauri et al. (2016) Topical Mitomycin-C enhances subbasal nerve regeneration and reduces erosion frequency in the debridement wounded mouse cornea. Exp Eye Res 146:361-9
Sriram, Sriniwas; Tran, Jennifer A; Zieske, James D (2016) Cornea As a Model for Testing CTGF-Based Antiscarring Drugs. Bone Tissue Regen Insights 7:
Stepp, Mary Ann; Zieske, James D; Trinkaus-Randall, Vickery et al. (2014) Wounding the cornea to learn how it heals. Exp Eye Res 121:178-93

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