4.7 Article

Arsenic retention in erythrocytes and excessive erythrophagocytosis is related to low selenium status by impaired redox homeostasis

期刊

REDOX BIOLOGY
卷 52, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.redox.2022.102321

关键词

Arsenic; Selenium; Erythrocyte; Oxidative stress; Erythrophagocytosis

资金

  1. National Natural Science Foundation of China [81870323]
  2. Natural Science Foundation of Guangdong Province [2021A1515010104, 2022A1515010253]
  3. Project of Science and Technology of Guangdong Province [2018A050506041]
  4. Project of Science and Technology of Guangzhou [202206010033]
  5. Project of Guangdong Agricultural Commissioner (2020)

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Arsenic contamination in drinking water is a global public health problem. Selenium deficiency is associated with an increased risk of arsenism. This study found that low Se status impairs redox homeostasis, leading to increased As retention in erythrocytes and subsequent phagocytosis by splenic macrophages, resulting in increased inflammatory response.
Arsenic (As) contamination in drinking water is a global public health problem. Epidemiological studies have shown that selenium (Se) deficiency is associated with an increasing risk of arsenism. However, the association between Se status and As retention in erythrocytes and mechanisms underlying this association have not been fully investigated. In the present study, a total of 165 eligible subjects were recruited and As was found to accumulate in blood mainly by retention in erythrocytes. Retention of As in erythrocytes was negatively correlated with Se status, antioxidant parameters related to Se and As methylation capacity, but positively correlated with the protein-binding capacity of As. Additionally, erythrocytes isolated from subjects with low Se status exhibited cellular damage along with lower protein levels of CD47, which could be aggravated by hydrogen peroxide treatment. Consistent with the human study, the erythrocytes from mice with sub-chronic As exposure exhibited similar cellular damage and shown to be phagocytosed by splenic macrophages, and these effects were mitigated by dietary Se supplementation. Furthermore, hydrogen peroxide treatment induced excessive phagocytosis of erythrocytes with As exposure by splenic macrophages, while co-treating erythrocytes with the reducing agent, N-Acetyl-L-cysteine, mitigated this excessive erythrophagocytosis. Hyperactivation of the NFiB pathway was also detected in splenic macrophages after excessive erythrophagocytosis. In conclusion, this study found that low Se status involving impaired redox homeostasis increased As retention in erythrocytes, which were subsequently phagocytosed by splenic macrophages and led to an increased inflammatory status of splenic macrophages. These findings provide insight into physiological features of arsenism related to Se status and redox homeostasis.

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