Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Study of the effect of the integration of photobiomodulation in LED lights on immortalised retinal cells.
Author Affiliations & Notes
  • Susana del Olmo Aguado
    Instituto Universitario Fernández-Vega (Fundación de Investigación Oftalmológica & Universidad de Oviedo), Spain
    Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain
  • Carla Martin Cueto
    Instituto Universitario Fernández-Vega (Fundación de Investigación Oftalmológica & Universidad de Oviedo), Spain
    Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain
  • Amador Menéndez-Velázquez
    Photoactive Materials Research Unit, Fundacion IDONIAL, Gijon, Asturias, Spain
  • Dolores Morales
    Photoactive Materials Research Unit, Fundacion IDONIAL, Gijon, Asturias, Spain
  • Ana Belén García-Delgado
    Photoactive Materials Research Unit, Fundacion IDONIAL, Gijon, Asturias, Spain
  • Miguel García
    Normagrup, Spain
  • Jesus Merayo-Lloves
    Instituto Universitario Fernández-Vega (Universidad de Oviedo & Fund. de Investigación Oftalmológica), Spain
    Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain
  • Mikel Jaureguizar
    Normagrup, Spain
  • Footnotes
    Commercial Relationships   Susana del Olmo Aguado None; Carla Martin Cueto None; Amador Menéndez-Velázquez None; Dolores Morales None; Ana Belén García-Delgado None; Miguel García Normagrup, Code E (Employment); Jesus Merayo-Lloves None; Mikel Jaureguizar Normagrup, Code E (Employment)
  • Footnotes
    Support  IDE/2021/000508 (IDEPA and PCTI. Fondo Europeo de Desarrollo Regional (FEDER))
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 6744. doi:
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      Susana del Olmo Aguado, Carla Martin Cueto, Amador Menéndez-Velázquez, Dolores Morales, Ana Belén García-Delgado, Miguel García, Jesus Merayo-Lloves, Mikel Jaureguizar; Study of the effect of the integration of photobiomodulation in LED lights on immortalised retinal cells.. Invest. Ophthalmol. Vis. Sci. 2024;65(7):6744.

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

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Abstract

Purpose : The period of time that our visual system is exposed to artificial light is increasing. This prolonged exposure to light sources has implications for eye health. The development of lighting systems based on photobiomodulation (PBM), that do not alter the colour rendering index (CRI), may result in significant benefits for the population. This study examined the effect of exposure to a new lighting system on a retinal in vitro model.

Methods : ARPE-19 cells were seeded in 96-well plates at 10000 cells/mL. Three experimental groups were established: 1) a control group of cells maintained in the dark, 2) a group of cells exposed to white LED-type illumination (standard light, 1000 lux), and 3) a group of cells exposed to the developed illumination device (NO7D ligth,1000 lux). ARPE-19 cells were maintained under these experimental conditions for a period of 48 hours. At the end of the exposure period, cell viability was assessed using the WST-1 kit. In addition, the response to oxidative damage (HO-1) and the maintenance of the structural integrity of the monolayer (ZO-1, occludin, b-catenin) were studied by immunochemical techniques.

Results : Prolonged exposure to the conventional LED device resulted in oxidative damage and reduced cell viability. In contrast, the use of the PBM-based device showed similar cell viability to the control group. HO-1 expression was maintained at levels similar to the control group. However, a greater response in the expression of markers of different types of intercellular junctions was observed in cells exposed to the device in contrast to cells kept in the dark.

Conclusions : A PBM-based lighting system can be useful in maintaining eye health.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

A) Quantification of cell viability determined the WST-1 assay. Tukey's multiple comparisons test shows significant differences, ** p<0.05 and **** p<0.001. Results are expressed as mean value ± SEM where N=6. B) Immunofluorescence for ZO-1 (red). Standard light causes a reduction in tight junctions (arrowhead). NO7D light shows increased expression of ZO-1 compared to the control group. Nuclei are labelled with DAPI (blue). Scale: 50 microns.

A) Quantification of cell viability determined the WST-1 assay. Tukey's multiple comparisons test shows significant differences, ** p<0.05 and **** p<0.001. Results are expressed as mean value ± SEM where N=6. B) Immunofluorescence for ZO-1 (red). Standard light causes a reduction in tight junctions (arrowhead). NO7D light shows increased expression of ZO-1 compared to the control group. Nuclei are labelled with DAPI (blue). Scale: 50 microns.

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