• Medientyp: E-Book
  • Titel: Mechanism of Interleukin-33 Up-Regulation Caused by 1,4-Naphthoquinone Black Carbon in Raw264.7 Cells
  • Beteiligte: Li, Zekang [Verfasser:in]; Jiang, Wanyu [Verfasser:in]; Chu, Hongqian [Verfasser:in]; Ge, Jianhong [Verfasser:in]; Wang, Xiaoyun [Verfasser:in]; Jiang, Jianjun [Verfasser:in]; Xiao, Qianqian [Verfasser:in]; Meng, Qinghe [Verfasser:in]; Hao, Weidong [Verfasser:in]; Wei, Xuetao [Verfasser:in]
  • Erschienen: [S.l.]: SSRN, [2022]
  • Umfang: 1 Online-Ressource (30 p)
  • Sprache: Englisch
  • DOI: 10.2139/ssrn.4029223
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  • Beschreibung: BackgroundAs air pollution has been paid more attention to by public in recent years, effects and mechanism in particulate matter-triggered health problems become a focus of research. Lysosomes and mitochondria play an important role in regulation of inflammation. Interleukin-33 (IL-33) has been proved to promote inflammation in our previous studies. In this study, macrophage cell line RAW264.7 was used to explore the mechanism of IL-33 up-gradation, effects on lysosomes and mitochondria induced by 1,4-naphthoquinone black carbon (1,4-NQ-BC).Results50μg/mL 1,4-NQ-BC exposure for 24 h dramatically increased expression of IL-33 in RAW264.7 cells. Lysosomal membrane permeability was damaged by 1,4-NQ-BC treatment, and higher mitochondrial membrane potential and ROS level were induced by 1,4-NQ-BC. The results of proteomics suggested that expression of ferritin light chain was increased after cells were challenged with 1,4-NQ-BC, and it was verified by Western blot. Meanwhile, expressions of p62 and LC3B-II were increased by 50μg/mL 1,4-NQ-BC in RAW264.7 cells. Ultimately, expression of IL-33 could return to same level as control in cells treated with 50μg/mL 1,4-NQ-BC and 50μM deferoxamine combined.Conclusions1,4-NQ-BC induces IL-33 upregulation in RAW264.7 cells, and it is responsible for higher lysosomal membrane permeability and ROS level, lower mitochondrial membrane potential, and inhibition of autophagy. Ferritin light chain possibly plays an important role in the upregulation of IL-33 evoked by 1,4-NQ-BC
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