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Article

Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence

  • Authors:
    • Seon Yeong Chae
    • Sun Young Park
    • Geuntae Park
  • View Affiliations / Copyright

    Affiliations: Department of Nanomaterials Engineering, Pusan National University, Busan 46241, Republic of Korea, Bio‑IT Fusion Technology Research Institute, Pusan National University, Busan 46241, Republic of Korea
  • Pages: 5182-5190
    |
    Published online on: October 8, 2018
       https://doi.org/10.3892/mmr.2018.9538
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Abstract

Oxidative stress‑induced cellular senescence is an important contributor to the pathogenesis of age‑related macular degeneration (AMD). Characteristics of premature cellular senescence include a loss of proliferation, change in cell shape, irreversible cell cycle arrest, and elevated senescence‑associated β‑galactosidase (SA‑β‑gal) activity. It was hypothesized that lutein may have anti‑senescence potential and may be useful as a treatment for AMD. In the present study, premature cellular senescence was induced in ARPE‑19 cells via treatment with H2O2 and the effects of lutein application were confirmed by observing cell morphology, lysosome contents, reactive oxygen species (ROS) generation and SA‑β‑gal activity, and cell cycle progression. The protein expression was also analyzed via western blotting in order to identify the affected signaling pathways. The results revealed that H2O2 treatment induced premature cellular senescence in ARPE‑19 cells, as evidenced by an increased production of ROS and SA‑β‑gal, altered lysosome contents, changed cellular morphology and arrested cell cycle progression. However, when treated with lutein, ARPE‑19 cells were effectively protected from these H2O2‑induced effects. Western blot analysis revealed that lutein induced the expression of heme oxygenase‑1, NAD(P)H quinone dehydrogenase 1, sirtuin (SIRT)‑1, and SIRT3. Together, the results indicated that lutein protects cells from cellular senescence induced by oxidative stress; therefore, it may be able to suppress the progression of AMD. In addition, our increased understanding of the pathways through which lutein acts is useful for the development of novel therapies for the treatment of oxidative stress‑associated retinal disease.
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Copy and paste a formatted citation
Spandidos Publications style
Chae SY, Park SY and Park G: Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence. Mol Med Rep 18: 5182-5190, 2018.
APA
Chae, S.Y., Park, S.Y., & Park, G. (2018). Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence. Molecular Medicine Reports, 18, 5182-5190. https://doi.org/10.3892/mmr.2018.9538
MLA
Chae, S. Y., Park, S. Y., Park, G."Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence". Molecular Medicine Reports 18.6 (2018): 5182-5190.
Chicago
Chae, S. Y., Park, S. Y., Park, G."Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence". Molecular Medicine Reports 18, no. 6 (2018): 5182-5190. https://doi.org/10.3892/mmr.2018.9538
Copy and paste a formatted citation
x
Spandidos Publications style
Chae SY, Park SY and Park G: Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence. Mol Med Rep 18: 5182-5190, 2018.
APA
Chae, S.Y., Park, S.Y., & Park, G. (2018). Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence. Molecular Medicine Reports, 18, 5182-5190. https://doi.org/10.3892/mmr.2018.9538
MLA
Chae, S. Y., Park, S. Y., Park, G."Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence". Molecular Medicine Reports 18.6 (2018): 5182-5190.
Chicago
Chae, S. Y., Park, S. Y., Park, G."Lutein protects human retinal pigment epithelial cells from oxidative stress‑induced cellular senescence". Molecular Medicine Reports 18, no. 6 (2018): 5182-5190. https://doi.org/10.3892/mmr.2018.9538
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