May 2007
Volume 48, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2007
Adenoviral Gene Transfer of Smad7 Suppresses Epithelial-Mesenchymal Transition and Fibrogenic Reaction by Corneal Endothelium Post-Alkali-Burn in Rats
Author Affiliations & Notes
  • T. Sumioka
    Ophthalmology, Wakayama Medical University, Wakayama, Japan
  • S. Saika
    Ophthalmology, Wakayama Medical University, Wakayama, Japan
  • K. Ikeda
    Anatomy, Osaka City University, Osaka, Japan
  • Y. Okada
    Ophthalmology, Wakayama Medical University, Wakayama, Japan
  • O. Yamanaka
    Ophthalmology, Wakayama Medical University, Wakayama, Japan
  • Y. Ohnishi
    Ophthalmology, Wakayama Medical University, Wakayama, Japan
  • Footnotes
    Commercial Relationships T. Sumioka, None; S. Saika, None; K. Ikeda, None; Y. Okada, None; O. Yamanaka, None; Y. Ohnishi, None.
  • Footnotes
    Support None.
Investigative Ophthalmology & Visual Science May 2007, Vol.48, 2698. doi:
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    • Get Citation

      T. Sumioka, S. Saika, K. Ikeda, Y. Okada, O. Yamanaka, Y. Ohnishi; Adenoviral Gene Transfer of Smad7 Suppresses Epithelial-Mesenchymal Transition and Fibrogenic Reaction by Corneal Endothelium Post-Alkali-Burn in Rats. Invest. Ophthalmol. Vis. Sci. 2007;48(13):2698.

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

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Abstract

Purpose:: To examine if overexpression of Smad7 by adenoviral gene transfer suppresses epithelial-mesenchymal transition and subsequent fibrogenic reaction by corneal endothelium in an alkali-burned cornea in rats. Such reaction causes formation of retrocorneal membrane in an alkali-burned cornea.

Methods:: Two adenoviral vectors carrying Cre recombinase under CAG promoter and Smad7 cDNA under LNL promoter, mixed with hyaluronan, were applied to the anterior chamber of adult Wistar rats (n = 14) under general anesthesia. Control animals received a vector of CAG/Cre recombinase. After 3 days the eye received 10 microL of 1N NaOH. After specific interval of healing the animals were killed and the eye was processed for histology/immunohistochemistry for α-smooth muscle actin (αSMA) and collagen I. Efficacy of gene transfer was evaluated by the vector carrying green fluorescein protein (GFP).

Results:: GFP was detected in corneal endothelium. In control healing cornea αSMA was expressed in stromal fibroblasts and corneal endothelium. Collagen I was also seen in endothelium. Expression of αSMA and collagen I was suppressed in corneal endothelium.

Conclusions:: Smad7 overexpression suppresses epithelial-mesenchymal transition and subsequent fibrogenic reaction by corneal endothelium in an alkali-burned cornea in rats.

Keywords: cornea: endothelium • gene transfer/gene therapy • wound healing 
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