DISTRIBUTION OF GROWTH-FACTORS IN SUBFOVEAL NEOVASCULAR MEMBRANES IN AGE-RELATED MACULAR DEGENERATION AND PRESUMED OCULAR HISTOPLASMOSIS SYNDROME

被引:78
作者
REDDY, VM [1 ]
ZAMORA, RL [1 ]
KAPLAN, HJ [1 ]
机构
[1] WASHINGTON UNIV, SCH MED, DEPT OPHTHALMOL & VISUAL SCI, ST LOUIS, MO 63110 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0002-9394(14)72158-0
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: 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. METHODS: 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. RESULTS: Most cells in subfoveal neovascular membranes are retinal pigment epithelial cells and cells resembling fibroblasts, with some vascular endothelial cells, lymphocytes, and macrophages. Basic fibroblast 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. CONCLUSIONS: 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.
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页码:291 / 301
页数:11
相关论文
共 31 条
[11]  
GROSSNIKLAUS HE, 1994, OPHTHALMOLOGY, V101, P1099
[12]  
GROSSNIKLAUS HE, 1989, AM J OPHTHALMOL, V114, P221
[13]   ALTERED DISTRIBUTION OF BASIC FIBROBLAST GROWTH-FACTOR IN DIABETIC-RETINOPATHY [J].
HANNEKEN, A ;
DEJUAN, E ;
LUTTY, GA ;
FOX, GM ;
SCHIFFER, S ;
HJELMELAND, LM .
ARCHIVES OF OPHTHALMOLOGY, 1991, 109 (07) :1005-1011
[14]   MITOGENIC EFFECT OF TRANSFORMING GROWTH FACTOR-BETA-1 ON HUMAN FIBROBLASTS INVOLVES THE INDUCTION OF PLATELET-DERIVED GROWTH FACTOR-ALPHA RECEPTORS [J].
ISHIKAWA, O ;
LEROY, EC ;
TROJANOWSKA, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 145 (01) :181-186
[15]  
KORTE GE, 1989, INT REV CYTOL, V114, P221
[16]  
LUTTY GA, 1993, INVEST OPHTH VIS SCI, V34, P477
[17]   FIBROBLAST GROWTH-FACTOR PHOSPHORYLATION AND RECEPTORS IN ROD OUTER SEGMENTS [J].
MASCARELLI, F ;
RAULAIS, D ;
COURTOIS, Y .
EMBO JOURNAL, 1989, 8 (08) :2265-2273
[18]   A MONOCLONAL-ANTIBODY TO THE CARBOXYTERMINAL DOMAIN OF PROCOLLAGEN TYPE-1 VISUALIZES COLLAGEN-SYNTHESIZING FIBROBLASTS - DETECTION OF AN ALTERED FIBROBLAST PHENOTYPE IN LUNGS OF PATIENTS WITH PULMONARY FIBROSIS [J].
MCDONALD, JA ;
BROEKELMANN, TJ ;
MATHEKE, ML ;
CROUCH, E ;
KOO, M ;
KUHN, C .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (05) :1237-1244
[19]  
MERWIN JR, 1991, AM J PATHOL, V138, P37
[20]  
MILLER JW, 1994, AM J PATHOL, V145, P574