Chitooligosaccharide prevents vascular endothelial cell apoptosis by attenuation of endoplasmic reticulum stress via suppression of oxidative stress through Nrf2-SOD1 up-regulation

Pharm Biol. 2022 Dec;60(1):2155-2166. doi: 10.1080/13880209.2022.2133150.

Abstract

Context: Endoplasmic reticulum (ER) stress contributes to endothelium pathological conditions. Chitooligosaccharides (COS) have health benefits, but their effect on endothelial cells is unknown. We demonstrate for the first time a protective effect of COS against ER-induced endothelial cell damage.

Objective: To evaluate the protective effect of COS on ER stress-induced apoptosis in endothelial cells.

Material and methods: Endothelial (EA.hy926) cells were pre-treated with COS (250 or 500 μg/mL) for 24 h, and then treated with 0.16 μg/mL of Tg for 24 h and compared to the untreated control. Apoptosis and necrosis were detected by Annexin V-FITC/propidium iodide co-staining. Reactive oxygen species (ROS) were measured with the DCFH2-DA and DHE probes. The protective pathway and ER stress markers were evaluated by reverse transcription-polymerase chain reaction, western blot, and immunofluorescence analyses.

Results: COS attenuated ER stress-induced cell death. The viability of EA.hy926 cells treated with Tg alone was 44.97 ± 1% but the COS pre-treatment increased cells viability to 74.74 ± 3.95% in the 250 μg/mL COS and 75.34 ± 2.4% in the 500 μg/mL COS treatments. Tg induced ER stress and ROS, which were associated with ER stress-mediated death. Interestingly, COS reduced ROS by upregulating nuclear factor-E2-related factor 2 (Nrf2), and the oxidative enzymes, superoxide dismutase1 (SOD1) and catalase. COS also suppressed up-regulation of the ER-related apoptosis protein, CHOP induced by Tg.

Conclusions: COS protected against ER stress-induced apoptosis in endothelial cells by suppressing ROS and up-regulation Nrf2 and SOD1. These findings support the use of COS to protect endothelial cells.

Keywords: CHOP; ER stress; ROS; antioxidant; chitosan; shrimp shell.

MeSH terms

  • Apoptosis
  • Catalase / metabolism
  • Endoplasmic Reticulum Stress*
  • Endothelial Cells
  • NF-E2-Related Factor 2* / metabolism
  • Oxidative Stress
  • Propidium / metabolism
  • Propidium / pharmacology
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase-1 / genetics
  • Superoxide Dismutase-1 / metabolism
  • Superoxide Dismutase-1 / pharmacology
  • Superoxides / metabolism
  • Up-Regulation

Substances

  • NF-E2-Related Factor 2
  • Reactive Oxygen Species
  • Superoxides
  • Catalase
  • Superoxide Dismutase-1
  • Propidium

Grants and funding

Financial support from National Science and Technology Development Agency for Chair Professor Grant [Grant no. P-20-52297].