April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Epogen Receptor Expression in Human Diabetic Retina
Author Affiliations & Notes
  • S. S. Shah
    Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa
    Omics Laboratory, Iowa City, Iowa
  • S. S. Tsang
    Omics Laboratory, Iowa City, Iowa
    Department of Ophthalmology, Columbia University, New York, New York
  • V. B. Mahajan
    Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa
    Omics Laboratory, Iowa City, Iowa
  • Footnotes
    Commercial Relationships  S.S. Shah, None; S.S. Tsang, None; V.B. Mahajan, None.
  • Footnotes
    Support  Research to Prevent Blindness
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 5379. doi:
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      S. S. Shah, S. S. Tsang, V. B. Mahajan; Epogen Receptor Expression in Human Diabetic Retina. Invest. Ophthalmol. Vis. Sci. 2009;50(13):5379.

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

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Abstract

Purpose: : Erythropoietin (EPO) is a potent angiogenic factor associated with proliferative diabetic retinopathy. This study was performed to identify erythropoietin receptor (EPOR) mRNA expression in the human diabetic eye.

Methods: : Post-mortem retinas were obtained from human eyes with and without diabetic retinopathy. Anti-sense RNA and control sense probes were generated from a human EPOR cDNA template. After in situ hybridization, expression patterns of EPOR mRNA were studied with darkfield and phase contrast microscopy.

Results: : EPOR antisense probes were successfully validated on human pancreas tissue. In the eye, EPOR was expressed in the retinal ganglion cell layer. No expression was observed in the inner or outer nuclear layer. There was no significant difference in the expression patterns observed in normal and diabetic human eyes.

Conclusions: : EPOR expression in retinal ganglion cells is not altered in a human eye with very severe proliferative diabetic retinopathy.

Keywords: diabetic retinopathy • ischemia • gene/expression 
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