December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Analysis of Fibronectin EDA Expression in RPE Cells Exposed to Growth Factors
Author Affiliations & Notes
  • R Khankan
    Doheny Eye Institute and the Department of Ophthalmology Keck School of Medicine at the University of Southern California Los Angeles CA
  • C Spee
    Doheny Eye Institute and the Department of Ophthalmology Keck School of Medicine at the University of Southern California Los Angeles CA
  • SJ Ryan
    Doheny Eye Institute and the Department of Ophthalmology Keck School of Medicine at the University of Southern California Los Angeles CA
  • DR Hinton
    Doheny Eye Institute and the Department of Ophthalmology Keck School of Medicine at the University of Southern California Los Angeles CA
  • Footnotes
    Commercial Relationships   R. Khankan, None; C. Spee, None; S.J. Ryan, None; D.R. Hinton, None. Grant Identification: NIH grants EY03040 and EY01545; Research to Prevent Blindness; Arnold and Mabel Beckman Foundation
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 4573. doi:
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    • Get Citation

      R Khankan, C Spee, SJ Ryan, DR Hinton; Analysis of Fibronectin EDA Expression in RPE Cells Exposed to Growth Factors . Invest. Ophthalmol. Vis. Sci. 2002;43(13):4573.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose:Retinal pigment epithelial (RPE) cells are among cellular constituents thought to be involved in both proliferative vitreoretinopathy and age-related macular degeneration. Their activation in response to injury is mediated by extracellular matrix (ECM) growth factors and cytokines. Fibronectin (FN) EDA is an alternatively spliced embryonic isoform that has been implicated in cellular migration during development and wound healing. The effect of various growth factors on FN EDA expression in fetal RPE cells is investigated here. Methods:FN EDA expression in human fetal RPE cell cultures exposed to different growth factors was studied by Western blot and by immunohistochemical analysis using a FN EDA-specific monoclonal antibody. Both cell supernatants and homogenates were examined. Results:Expression of FN EDA was detected in cultures of fetal RPE cells stimulated with either transforming growth factor-ß (TGFß) or vascular endothelial growth factor (VEGF). Other growth factors tested (hepatocyte-, fibroblast-, and platelet-derived growth factors) had no effect on FN EDA expression. Conclusion:The results of this study suggest that FN EDA expression might be up-regulated in disorders in which TGFß and VEGF are expressed and may therefore contribute to the pathogenesis of these disorders.

Keywords: 567 retinal pigment epithelium • 423 growth factors/growth factor receptors • 507 pathology: human 
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