4.7 Article

Blue Light Induces Impaired Autophagy through Nucleotide-Binding Oligomerization Domain 2 Activation on the Mouse Ocular Surface

期刊

出版社

MDPI
DOI: 10.3390/ijms22042015

关键词

blue light; nucleotide-binding oligomerization domain 2; autophagy related 16 like 1; autophagy; apoptosis

资金

  1. Chonnam National University Hospital Biomedical Research Institute [BCRI 19038]
  2. National Research Foundation of Korea [NRF2020R 1F 1A 1061179]

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This study investigated the effects of blue light exposure on NOD2 expression and autophagy in mice ocular surface. The findings suggest that blue light exposure activates NOD2, leading to impaired autophagy and corneal epithelial apoptosis. NOD2-KO mice showed lower levels of autophagic impairment and epithelial damage after blue light exposure.
In this study, we investigated the effects of blue light exposure on nucleotide-binding oligomerization domain 2 (NOD2) expression on the mouse ocular surface and evaluated the role of NOD2 activation in light-induced cell death. Mice were divided into wild-type (WT), NOD2-knock out (KO), WT + blue light (WT + BL), and NOD2-KO + blue light (NOD2-KO + BL) groups, and the mice in the WT+BL and NOD2-KO + BL groups were exposed to blue light for 10 days. After 10 days of blue light exposure, increased reactive oxygen species and malondialdehyde were observed in the WT + BL and NOD2-KO + BL groups, and the WT + BL group showed a higher expression of NOD2 and autophagy related 16 like 1. Although both WT+BL and NOD2-KO + BL groups showed an increase in the expression of light chain 3-II, NOD2-KO + BL mice had a significantly lower p62 expression than WT + BL mice. In addition, NOD2-KO+BL mice had significantly lower corneal epithelial damage and apoptosis than WT + BL mice. In conclusion, blue light exposure can induce impaired autophagy by activation of NOD2 on the ocular surface. In addition, the reactive oxygen species (ROS)-NOD2-autophagy related 16 like 1 (ATG16L) signaling pathway may be involved in the blue-light-induced autophagy responses, resulting in corneal epithelial apoptosis.

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