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PMID: 7661200 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Distribution of growth factors in subfoveal neovascular membranes in age-related macular degeneration and presumed ocular histoplasmosis syndrome.

American journal of ophthalmology ·Vol. 120 ·No. 3 ·1995-09-00 ·Pages 291-301

Reddy VM, Zamora RL, Kaplan HJ

Abstract

We performed a histopathologic and immunohistologic study to determine the macromolecular and cellular components of subfoveal neovascular membranes removed at the time of submacular surgery. Subfoveal neovascular membranes were surgically removed from ten patients (seven with age-related macular degeneration and three with presumed ocular histoplasmosis syndrome). Tissues obtained were examined by light and electron microscopy to identify structural components. Immunohistochemical staining was then performed with monoclonal antibodies to various growth factors, including transforming growth factor-beta 1, basic fibroblast growth factor, platelet-derived growth factor, and epidermal growth factor, as well as antibodies against procollagen 1 and phosphotyrosine residues. Most cells in subfoveal neovascular membranes are retinal pigment epithelial cells and cells resembling fibroblasts, with some vascular endothelial cells, lymphocytes, and macrophages. Basic fibroblasts growth factor was found in the extracellular matrix and in endothelial cells. Transforming growth factor-beta 1 was found in endothelial cells, fibroblasts, and retinal pigment epithelial cells. Procollagen 1 was found in protein-synthesizing fibroblasts, and phosphotyrosine residues were detected within fibroblasts, endothelial cells, and retinal pigment epithelial cells. Subfoveal neovascular membranes are neovascular complexes composed of retinal pigment epithelial cells, fibroblasts, vascular endothelial cells, and chronic inflammatory cells. Furthermore, transforming growth factor-beta 1 and basic fibroblast growth factor are present within the major cell types, which suggests a possible pathogenic role in the development of the neovascular complex.

MeSH Terms
Adult Aged Aged, 80 and over Antibodies, Monoclonal Cell Membrane/metabolism,pathology Endothelium, Vascular/metabolism,pathology Eye Infections, Fungal/complications Female Fibroblasts/metabolism,pathology Fovea Centralis/metabolism,pathology Growth Substances/metabolism Histoplasmosis/complications Humans Immunoenzyme Techniques Lymphocytes/metabolism,pathology Macrophages/metabolism,pathology Macular Degeneration/complications Male Middle Aged Pigment Epithelium of Eye/metabolism,pathology Retinal Neovascularization/etiology,metabolism,pathology,surgery Syndrome
Chemicals
Antibodies, Monoclonal Growth Substances
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Reddy V M
Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, USA.
Zamora R L
Kaplan H J
Article Info
Journal
American journal of ophthalmology
Abbr.
Am J Ophthalmol
ISSN
0002-9394
Published
1995-09-00
Pages
291-301
Language
English
Region
United States
NLM ID
0370500
Subset
IM
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