May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Induction of Eotaxin–3 Expression in Human Retinal Pigmented Epithelial Cells by TNF– and VEGF–A.
Author Affiliations & Notes
  • J.Z. Baffi
    Department of Ophthalmology & Visual Sciences, University of Kentucky, Lexington, KY
  • E. Sakurai
    Department of Ophthalmology & Visual Sciences, University of Kentucky, Lexington, KY
  • B.K. Ambati
    Department of Ophthalmology, Medical College of Georgia, Augusta, GA
  • J. Ambati
    Department of Ophthalmology & Visual Sciences, University of Kentucky, Lexington, KY
  • Footnotes
    Commercial Relationships  J.Z. Baffi, None; E. Sakurai, None; B.K. Ambati, None; J. Ambati, None.
  • Footnotes
    Support  NIH–NIDCD Training Grant T32–DC–00065
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 1804. doi:
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      J.Z. Baffi, E. Sakurai, B.K. Ambati, J. Ambati; Induction of Eotaxin–3 Expression in Human Retinal Pigmented Epithelial Cells by TNF– and VEGF–A. . Invest. Ophthalmol. Vis. Sci. 2004;45(13):1804.

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

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Abstract

Abstract: : Purpose:To investigate the effects of tumor necrosis factor (TNF)–α and vascular endothelial growth factor (VEGF)–A alone, or in combination, on human retinal pigmented epithelial (hRPE) cell expression of the chemokine eotaxin–3, which has the exceptional property to actively repulse recruited monocytes. Methods: Serum–starved cultured hRPE cells were incubated with TNF–α, VEGF–A, or both. Eotaxin–3 mRNA expression in cell lysates was determined by reverse transcription–polymerase chain reaction analysis after 4 and 8 hours incubation. Results: hRPE cells incubated either in the absence of cytokines or with VEGF–A alone did not express detectable amounts of eotaxin–3 mRNA. Eotaxin–3 mRNA expression, which was stimulated by TNF–α alone in a time–dependent fashion peaking at 4 hours, was further upregulated by preincubation with VEGF–A. Conclusions:The synergistic effect of TNF–α and VEGF–A on eotaxin–3 mRNA expression by hRPE cells suggests a role for this chemokine in modulating macrophage trafficking in the subretinal space.

Keywords: retinal pigment epithelium • cytokines/chemokines 
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