To preserve the integrity of the corneal epithelium it is essential to maintain a transparent and refractile medium. Persistent epithelial defects and recurrent cornea erosions are painful and may occur if the integrity of the corneal surface is challenged by injury or disease. Epithelial healing becomes compromised when disorders in the adhesion of corneal epithelial cells are prevalent. The overall goal of this proposal is to examine interactions between epithelial cells and their underlying extracellular matrix. We have shown that these interactions influence the localization and expression of adhesion proteins. Specifically, the aims of the project are to: 1). analyze the regulation of adhesion and cytoskeletal proteins by corneal substrata, 2). analyze changes in cytoplasmic pH and Ca2+ in vitro in response to changes in substrata and 3). analyze the role of phosphorylation in cell-matrix interactions. The adhesion assay developed by the applicant will be used as a vehicle to examine these interactions. To achieve the aims we will analyze the expression of adhesion receptors and intracellular signalling events on mechanically altered, chemically altered and photoablate corneal substrata. The responses will be correlated with changes in the formation of adhesion structures and cytoarchitecture. By understanding the interactions between epithelial cells and their substrate, one can develop new modes of therapy aimed at indolent epithelial defects of the cornea.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY006000-12
Application #
2430328
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1986-06-01
Project End
1998-05-31
Budget Start
1997-06-01
Budget End
1998-05-31
Support Year
12
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Boston University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Lee, Albert; Karamichos, Dimitrios; Onochie, Obianamma E et al. (2018) Hypoxia modulates the development of a corneal stromal matrix model. Exp Eye Res 170:127-137
Kneer, Krisandra; Green, Michael B; Meyer, Jenna et al. (2018) High fat diet induces pre-type 2 diabetes with regional changes in corneal sensory nerves and altered P2X7 expression and localization. Exp Eye Res 175:44-55
Minns, Martin S; Trinkaus-Randall, Vickery (2016) Purinergic Signaling in Corneal Wound Healing: A Tale of 2 Receptors. J Ocul Pharmacol Ther 32:498-503
Minns, Martin S; Teicher, Gregory; Rich, Celeste B et al. (2016) Purinoreceptor P2X7 Regulation of Ca(2+) Mobilization and Cytoskeletal Rearrangement Is Required for Corneal Reepithelialization after Injury. Am J Pathol 186:285-96
Derricks, Kelsey E; Trinkaus-Randall, Vickery; Nugent, Matthew A (2015) Extracellular matrix stiffness modulates VEGF calcium signaling in endothelial cells: individual cell and population analysis. Integr Biol (Camb) 7:1011-25
Sanderson, Julie; Dartt, Darlene A; Trinkaus-Randall, Vickery et al. (2014) Purines in the eye: recent evidence for the physiological and pathological role of purines in the RPE, retinal neurons, astrocytes, Müller cells, lens, trabecular meshwork, cornea and lacrimal gland. Exp Eye Res 127:270-9
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
Karamichos, D; Hutcheon, A E K; Rich, C B et al. (2014) In vitro model suggests oxidative stress involved in keratoconus disease. Sci Rep 4:4608
Lee, Albert; Derricks, Kelsey; Minns, Martin et al. (2014) Hypoxia-induced changes in Ca(2+) mobilization and protein phosphorylation implicated in impaired wound healing. Am J Physiol Cell Physiol 306:C972-85
Chi, Cheryl; Trinkaus-Randall, Vickery (2013) New insights in wound response and repair of epithelium. J Cell Physiol 228:925-9

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