June 2013
Volume 54, Issue 15
ARVO Annual Meeting Abstract  |   June 2013
Temperature-dependent response of retinal pigment epithelial cells to laser irradiation
Author Affiliations & Notes
  • Ralf Brinkmann
    Institute of Biomedical Optics, University of Luebeck, Luebeck, Germany
    Medical Laser Center Luebeck, Luebeck, Germany
  • Hisashi Iwami
    Department of Ophthalmology, Osaka City University, Osaka, Japan
  • Joachim Pruessner
    Institute of Biomedical Optics, University of Luebeck, Luebeck, Germany
  • Veit Danicke
    Medical Laser Center Luebeck, Luebeck, Germany
  • Yoko Miura
    Institute of Biomedical Optics, University of Luebeck, Luebeck, Germany
  • Footnotes
    Commercial Relationships Ralf Brinkmann, PVA (P); Hisashi Iwami, None; Joachim Pruessner, None; Veit Danicke, None; Yoko Miura, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 1809. doi:
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      Ralf Brinkmann, Hisashi Iwami, Joachim Pruessner, Veit Danicke, Yoko Miura; Temperature-dependent response of retinal pigment epithelial cells to laser irradiation. Invest. Ophthalmol. Vis. Sci. 2013;54(15):1809.

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

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Purpose: Sublethal thermal therapy of the retinal pigment epithelium (RPE) is discussed as a new prophylactic therapy for age-related macular degeneration. However, temperature-dependent RPE cell effects have not been well elucidated. We investigated the biochemical responses of RPE cells following sublethal to lethal thermal laser irradiation.

Methods: Porcine RPE cells cultured in a dish (33mm) were heated with a Thulium laser (1.92µm, 1-20W, 10s) over a spot of 3mm. Temperatures during irradiation were measured with thermocouples. Cell viability was examined using annexin-V, ethidium homodimer III and Hoechst 33342 for detecting apoptotic, necrotic and living cell, respectively, by using fluorescence microscopy for localization and flow cytometry for quantification. Secretion of vascular endothelial growth factor (VEGF) for 6h following irradiation on different temperatures was assessed with Elisa assay. In order to examine a protective effect of sublethal hyperthremia, the cells were heated up to 45C 24h prior to the exposure of 2 mM hydroxyl peroxide (H2O2) for 5 h. The involvement of TRPV (Transient Receptor Potential Vanilloid)-1 receptor, which is activated with temperatures > 43C, was investigated by adding capsazepin, a TRPV-1 inhibitor, before irradiation.

Results: Cell apoptosis and necrosis was observed 24 h after irradiation with a central peak temperature ≥52C. Fluorescence microscopy revealed apoptotic cells around the central necrotic area. VEGF secretion for 6h after irradiation was significantly increased at peak temperatures between 40 and 52C in a temperature dependent manner (max. 110%, p<0.05), whereas the total secretion decreases with temperatures > 52C. Pre-irradiation onto 45C significantly reduced H2O2-induced cell death after 5h compared to non-heated cells (total cell death: 15.6% to 10.2%, necrosis: 6% to 4 %, early apoptosis: 5.1% to 3.6%; p<0.01). These effects were not observed in the existence of capsazepin during laser irradiation.

Conclusions: The number of apoptotic and necrotic RPE cells increase at least over 24h following thermal laser irradiation. Sublethal temperatures between 40 and 52C seem to induce various cellular responses as VEGF secretion, which might be related to the protective effect against oxidative stress. Results with capsazepin suggest that TRPV-1 channel activation by hyperthermia is essential to exert this protective effect.

Keywords: 701 retinal pigment epithelium • 726 stress response • 578 laser  

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