April 1996
Volume 37, Issue 5
Free
Articles  |   April 1996
Laser trabeculoplasty induces stromelysin expression by trabecular juxtacanalicular cells.
Author Affiliations
  • D E Parshley
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
  • J M Bradley
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
  • A Fisk
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
  • A Hadaegh
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
  • J R Samples
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
  • E M Van Buskirk
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
  • T S Acott
    Casey Eye Institute, CERES, Oregon Health Sciences University, Portland, OR 97201, USA.
Investigative Ophthalmology & Visual Science April 1996, Vol.37, 795-804. doi:
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      D E Parshley, J M Bradley, A Fisk, A Hadaegh, J R Samples, E M Van Buskirk, T S Acott; Laser trabeculoplasty induces stromelysin expression by trabecular juxtacanalicular cells.. Invest. Ophthalmol. Vis. Sci. 1996;37(5):795-804.

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

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Abstract

PURPOSE: The mechanism by which laser trabeculoplasty reduces elevated intraocular pressure in primary open-angle glaucoma has been established. To test the hypothesis that trabecular extracellular matrix turnover is involved, stromelysin expression after laser treatment of anterior segment organ cultures was evaluated. METHODS: Argon laser trabeculoplasty, using typical clinical treatment parameters, was applied to anterior segment organ cultures. Stromelysin levels and activity were then evaluated at various times by immunoblots of Western transfers and by zymography. Stromelysin mRNA levels were evaluated by dot blot and by reverse transcription, followed by polymerase chain reaction amplification. Stromelysin protein was localized by immunohistochemistry, and image analysis was used for quantitation. Stromelysin mRNA was localized by in situ hybridization. RESULTS: Trabecular stromelysin protein, activity, and mRNA levels were detectably elevated by 8 hours and were several-fold higher by 24 hours after treatment. Stromelysin immunostaining was elevated dramatically in the juxtacanalicular and insert regions of the meshwork, but only modestly in other regions. Stromelysin mRNA increases also were localized primarily to these regions. The juxtacanalicular stromelysin immunostaining increase was sustained for at least 1 week, whereas the insert levels declined somewhat after day 2. CONCLUSIONS: A stromelysin increase, localized primarily to the juxtacanalicular region of the meshwork, the putative site of the aqueous humor outflow resistance, should degrade trabecular proteoglycans, the putative outflow resistance source, and allow their uptake and further degradation by the juxtacanalicular cells. If diminished juxtacanalicular extracellular matrix turnover is responsible for the glaucomatous reduction in aqueous humor outflow, an increase in stromelysin in this specific area of the meshwork should ameliorate the problem. Thus, the observations support the working hypothesis and may explain the efficacy of this treatment for glaucoma.

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