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The Effect of A2E on the Ca(2+)-PKC Signaling Pathway in Human RPE Cells Exposed to Blue Light

AIMS: In a model of blue light-induced damage in N-retinylidene-N-retinylethanolamine (A2E)-loaded human retinal pigment epithelial (RPE) cells, we examined the effect of A2E on the calcium (Ca(2+))-protein kinase C (PKC) signaling pathway. METHODS: Primary human RPE cells were cultured, and the cel...

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Detalles Bibliográficos
Autores principales: Luo, Maomei, Wang, Shu, Tang, Yun, Zeng, Chun, Cai, Shanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596233/
https://www.ncbi.nlm.nih.gov/pubmed/36304713
http://dx.doi.org/10.1155/2022/2233223
Descripción
Sumario:AIMS: In a model of blue light-induced damage in N-retinylidene-N-retinylethanolamine (A2E)-loaded human retinal pigment epithelial (RPE) cells, we examined the effect of A2E on the calcium (Ca(2+))-protein kinase C (PKC) signaling pathway. METHODS: Primary human RPE cells were cultured, and the cells in the 4th–6th passages were used in this study. The cells were divided into 5 groups: control cells (no A2E, no blue light), blue light-treated cells, blue light + chloroquine-treated cells, blue light + A2E-treated cells, and blue light + A2E + chloroquine-treated cells. The cells were first treated with chloroquine (15 μM for 12 h) and then loaded with A2E (25 μM for 2 h).The blue light intensity was 2000 ± 500 lux, and the duration was 6 h. After blue light exposure, the cells were cultured for 24 h. Fluo-3/AM staining was used to determine the level of cytoplasmic Ca(2+), and the cells were photographed using a laser scanning confocal microscope to analyze the fluorescence intensity. The intracellular levels of inositol triphosphate (IP3) and diacylglycerol (DAG) were measured by enzyme-linked immunosorbent assay (ELISA). Intracellular PKC activity was measured with a nonradioactive nuclide assay. RESULTS: Among all cell groups, the levels of Ca(2+), DAG, and IP3 were lowest in the control cells (P < 0.05). The Ca(2+), DAG, and IP3 levels in the blue light + A2E-treated cells and blue light + chloroquine-treated cells were higher than those in the blue light-treated cells (P < 0.05). The Ca(2+), DAG, and IP3 levels were highest in the blue light + A2E + chloroquine-treated group (P < 0.05). PKC activity was lowest in the control cells (P < 0.05). The PKC activity of the blue light + A2E-treated cells and blue light + chloroquine-treated cells was higher than that of the blue light-treated cells (P < 0.05), and the PKC activity of the blue light + A2E + chloroquine-treated cells was the highest (P < 0.05). CONCLUSION: Blue light and A2E increased the levels of Ca(2+), IP3, and DAG in human RPE cells and enhanced PKC activity, and blue light and A2E had a synergistic effect. Chloroquine further increased the levels of Ca(2+), IP3, and DAG and PKC activity in RPE cells or A2E-loaded RPE cells exposed to blue light.