Proliferative Vitreoretinopathy (PVR) is characterized by proliferation of retinal pigment epithelial (RPE) cells, fibroblasts and glial cells in the periretinal space following trauma. The proliferation of these cells results in the formation of a membrane which causes puckering and/or retraction of the retina. PVR is the major complication arising from retinal re- attachment surgery. Polypeptide growth factors control the rate of proliferation in normal human cells in a paracrine manner. In proliferative diseases, endogenous production of and response to growth factors may lead to increased rates of cellular proliferation in an autocrine fashion. In appropriate production of polypeptide growth factors by RPE cells which migrate into the periretinal space in PVR could contribute to the pathology of this disease. Alternatively, the cells which proliferate in PVR could respond to growth factors normally present in the retina. Therefore, the specific aims of this project include: 1) The development of a defined serum-free medium for the growth of RPE cells in vitro; 2) Expanded studies on the production of growth factors by cultured RPE cells; 3) Determining whether growth factors produced by RPE cells can stimulate the proliferation of RPE cells and fibroblasts in vitro; 4) Histological examination of normal and pathological specimens to determine the distribution and synthesis of growth factors in the posterior chamber of the eye.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY007373-04
Application #
3264322
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1989-05-01
Project End
1993-04-30
Budget Start
1992-05-01
Budget End
1993-04-30
Support Year
4
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Type
Schools of Medicine
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
Planck, S R; Rich, L F; Ansel, J C et al. (1997) Trauma and alkali burns induce distinct patterns of cytokine gene expression in the rat cornea. Ocul Immunol Inflamm 5:95-100
Rosenbaum, J T; Planck, S T; Huang, X N et al. (1995) Detection of mRNA for the cytokines, interleukin-1 alpha and interleukin-8, in corneas from patients with pseudophakic bullous keratopathy. Invest Ophthalmol Vis Sci 36:2151-5
Qu, Z; Huang, X N; Ahmadi, P et al. (1995) Expression of basic fibroblast growth factor in synovial tissue from patients with rheumatoid arthritis and degenerative joint disease. Lab Invest 73:339-46
Westra, I; Robbins, S G; Wilson, D J et al. (1995) Time course of growth factor staining in a rabbit model of traumatic tractional retinal detachment. Graefes Arch Clin Exp Ophthalmol 233:573-81
Robbins, S G; Mixon, R N; Wilson, D J et al. (1994) Platelet-derived growth factor ligands and receptors immunolocalized in proliferative retinal diseases. Invest Ophthalmol Vis Sci 35:3649-63
Qu, Z; Garcia, C H; O'Rourke, L M et al. (1994) Local proliferation of fibroblast-like synoviocytes contributes to synovial hyperplasia. Results of proliferating cell nuclear antigen/cyclin, c-myc, and nucleolar organizer region staining. Arthritis Rheum 37:212-20
Robbins, S G; Brem, R B; Wilson, D J et al. (1994) Immunolocalization of integrins in proliferative retinal membranes. Invest Ophthalmol Vis Sci 35:3475-85
Thompson, W S; Culbertson, W W; Smiddy, W E et al. (1994) Acute retinal necrosis caused by reactivation of herpes simplex virus type 2. Am J Ophthalmol 118:205-11
Planck, S R; Huang, X N; Robertson, J E et al. (1994) Cytokine mRNA levels in rat ocular tissues after systemic endotoxin treatment. Invest Ophthalmol Vis Sci 35:924-30
Brem, R B; Robbins, S G; Wilson, D J et al. (1994) Immunolocalization of integrins in the human retina. Invest Ophthalmol Vis Sci 35:3466-74

Showing the most recent 10 out of 20 publications