May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Expression of ADAM28 in Proliferative Diabetic Retinopathy
Author Affiliations & Notes
  • H. Shinoda
    Keio Univ. School of Medicine, Laboratory of Retinal Cell Biology, Department of Ophthalmology, Tokyo, Japan
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • M. Shimoda
    Keio Univ. School of Medicine, Department of Pathology, Tokyo, Japan
  • N. Nagai
    Keio Univ. School of Medicine, Laboratory of Retinal Cell Biology, Department of Ophthalmology, Tokyo, Japan
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • T. Koto
    Keio Univ. School of Medicine, Laboratory of Retinal Cell Biology, Department of Ophthalmology, Tokyo, Japan
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • S. Satofuka
    Keio Univ. School of Medicine, Laboratory of Retinal Cell Biology, Department of Ophthalmology, Tokyo, Japan
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • Y. Ozawa
    Keio Univ. School of Medicine, Laboratory of Retinal Cell Biology, Department of Ophthalmology, Tokyo, Japan
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • M. Inoue
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • K. Tsubota
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • Y. Okada
    Keio Univ. School of Medicine, Department of Pathology, Tokyo, Japan
  • S. Ishida
    Keio Univ. School of Medicine, Laboratory of Retinal Cell Biology, Department of Ophthalmology, Tokyo, Japan
    Keio Univ. School of Medicine, Department of Ophthalmology, Tokyo, Japan
  • Footnotes
    Commercial Relationships  H. Shinoda, None; M. Shimoda, None; N. Nagai, None; T. Koto, None; S. Satofuka, None; Y. Ozawa, None; M. Inoue, None; K. Tsubota, None; Y. Okada, None; S. Ishida, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 954. doi:
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    • Get Citation

      H. Shinoda, M. Shimoda, N. Nagai, T. Koto, S. Satofuka, Y. Ozawa, M. Inoue, K. Tsubota, Y. Okada, S. Ishida; Expression of ADAM28 in Proliferative Diabetic Retinopathy . Invest. Ophthalmol. Vis. Sci. 2006;47(13):954.

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

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Abstract

Purpose: : ADAM28 is a member of disintegrin and metalloproteinase (ADAM) family. Although ADAMs basically play roles in the ectodomain shedding of membrane proteins and cell adhesion, the function of ADAM28 remains to be elucidated. The aim of the present study was to investigate whether or not ADAM28 was associated with the pathogenesis of proliferative diabetic retinopathy (PDR).

Methods: : Tissue localization of ADAM28 in fibrovascular tissues, obtained at vitrectomy for patients with PDR, was examined by immunohistochemistry. Cultured human microvascular endothelial cells (HMVEC) were stimulated with 10µg/ml of vascular endothelial growth factor (VEGF) or vehicle alone for 24 hours. In vitro mRNA levels of ADAM28 were examined by semi–quantitative RT–PCR.

Results: : ADAM28 was localized on vascular endothelial cells in the fibrovascular tissue. mRNA levels of ADAM28 were substantially increased in VEGF–treated cells, compared to vehicle–treated cells.

Conclusions: : ADAM28 was expressed in the fibrocascular tissue of PDR and was upregulated by the stimulation of VEGF in vitro. These data suggest the involvement of ADAM28 in the pathogenesis of PDR.

Keywords: diabetic retinopathy • pathology: human • retina 
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