Study2012

Blueberry anthocyanins: protection against ageing and light-induced damage in retinal pigment epithelial cells

Liu Y, Song X, Zhang D, Zhou F, Wang D, Wei Y, Gao F, Xie L, Jia G, Wu W, Ji B

The British journal of nutrition · 55 citations

Review labels

Funding not disclosedMechanisms only

Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.

How it was studied

Design
In vitro/mechanistic study (classified by our AI screen)
Studied in
Cells or lab samples
Main outcome
Mechanisms only

Who paid for it

Funding
Funding not disclosed

Publication

Published
2011-10-12 · Br J Nutr · vol. 108 · issue 1 · pp. 16–27
Publisher
Cambridge University Press
Cited
88 citations · more than 89% of similar papers · 2.7× the field average
References
68 works
Access
Free to read
Research areas
Retinal Diseases and Treatments · Retinal Development and Disorders · Glaucoma and retinal disorders
Keywords
Apoptosis, Retinal pigment epithelium, Senescence, Anthocyanin, Retinal, Ageing, Viability assay, Biology, Cell biology, Pigment, Programmed cell death, Cell, Andrology, Cell damage, Molecular biology, Chemistry, Biochemistry, Botany, Medicine
MeSH
cell line, epithelial cells, humans, anthocyanins, vascular endothelial growth factor a, cell proliferation, gene expression regulation, aging, light, time factors, retinal pigment epithelium, blueberry plants

11 authors

From CN

  • Yixiang LiuChina Agricultural University
  • Xue SongChina Agricultural University
  • Di ZhangChina Agricultural University
  • Feng Li ZhouChina Agricultural University
  • Dan WangChina Agricultural University
  • Ying WeiChina Agricultural University

Abstract

Retinal pigment epithelium (RPE) cells are vital for retinal health. However, they are susceptible to injury with ageing and exposure to excessive light, including UV (100-380 nm) and visible (380-760 nm) radiation. To evaluate the protective effect of blueberry anthocyanins on RPE cells, in vitro cell models of replicative senescent and light-induced damage were established in the present study. After purification and fractionation, blueberry anthocyanin extracts (BAE) were yielded with total anthocyanin contents of 31·0 (SD 0·5) % and were used in this study. Replicative senescence of RPE cells was induced by repeatedly passaging cells from the fourth passage to the tenth. From the fifth passage, cultured RPE cells began to enter a replicative senescence, exhibiting reduced cell proliferation along with an increase in the number of β-galactosidase-positive cells. RPE cells maintained high cell viability (P < 0·01) and a low (P < 0·01) percentage of β-galactosidase-positive cells when treated with 0·1 μg/ml BAE. In contrast, after exposure to 2500 (SD 500) lx light (420-800 nm) for 12 h, RPE cells in the positive control (light exposure, no BAE treatment) exhibited premature senescence, low (P < 0·01) cell viability and increased (P < 0·01) vascular endothelial growth factor (VEGF) release compared with negative control cells, which were not subjected to light irradiation and BAE exposure. Correspondingly, BAE is beneficial to RPE cells by protecting these cells against light-induced damage through the suppression of ageing and apoptosis as well as the down-regulation of the over-expressed VEGF to normal level. These results demonstrate that BAE is efficacious against senescence and light-induced damage of RPE cells.

Abstract via Europe PMC. Copyright remains with the authors or publisher.

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