May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Differential Expression of Vitreous Proteins in Proliferative Diabetic Retinopathy
Author Affiliations & Notes
  • H.G. Yu
    Seoul National University, Seoul, Republic of Korea
    Ophthalmology,
  • S.J. Kim
    Seoul National University, Seoul, Republic of Korea
    Ophthalmology,
  • S. Kim
    Seoul National University, Seoul, Republic of Korea
    Molecular Genomic Medicine,
  • J.–M. Seo
    Seoul National University, Seoul, Republic of Korea
    Ophthalmology,
  • K.S. Park
    Seoul National University, Seoul, Republic of Korea
    Internal Medicine,
  • Y. Kim
    Seoul National University, Seoul, Republic of Korea
    Molecular Genomic Medicine,
  • Footnotes
    Commercial Relationships  H.G. Yu, None; S.J. Kim, None; S. Kim, None; J. Seo, None; K.S. Park, None; Y. Kim, None.
  • Footnotes
    Support  Ministry of the Health and Welfare of the Republic of Korea (02–PJ1–PG1–CH02–0003)
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 961. doi:
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    • Get Citation

      H.G. Yu, S.J. Kim, S. Kim, J.–M. Seo, K.S. Park, Y. Kim; Differential Expression of Vitreous Proteins in Proliferative Diabetic Retinopathy . Invest. Ophthalmol. Vis. Sci. 2006;47(13):961.

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

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Abstract

Purpose: : To identify vitreous proteins which were differentially expressed in patients suffering from proliferative diabetic retinopathy with active neovascularization.

Methods: : The vitreous samples of 15 active proliferative diabetic retinopathy patients were analyzed by two–dimensional gel electrophoresis and mass spectrometry, and the results were compared with those from age–matched patients with macular hole.

Results: : 25 protein spots were identified in the two–dimensional gel electrophoresis gels. Eight proteins in the 25 spots were expressed significantly differently between the macular hole and proliferative diabetic retinopathy patients (p value < 0.05). Five proteins were up–regulated in the proliferative diabetic retinopathy patients, and three were down–regulated (p value < 0.05).

Conclusions: : We constructed vitreous protein profiles for the proliferative diabetic retinopathy patients, and identified eight candidate proteins believed to be involved in the pathogenesis of proliferative diabetic retinopathy.

Keywords: vitreous • diabetic retinopathy • proteomics 
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