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Article

Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells

  • Authors:
    • Qihong Wu
    • Tianyu Miao
    • Ting Feng
    • Chuan Yang
    • Yingkun Guo
    • Hong Li
  • View Affiliations / Copyright

    Affiliations: Key Laboratory of Obstetrics and Gynecology and Pediatric Disease and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China, Department of Vascular Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China, Department of Radiology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China
  • Pages: 564-570
    |
    Published online on: May 4, 2018
       https://doi.org/10.3892/mmr.2018.8972
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Abstract

With the increase in applications of superparamagnetic iron oxide nanoparticles (SPIONs) in biomedicine, it is essential to investigate the bio‑security of these nanoparticles, especially with respect to the human immune system. In the present study, the biological effects of dextran‑coated superparamagnetic iron oxide nanoparticles (Dex‑SPIONs) on human primary monocyte cells were evaluated. The results of the present study demonstrated that Dex‑SPIONs can be identified in phagosomes or freed in the cytoplasm and did not affect cell viability or induce apoptosis. Notably, there were certain bulky vacuoles and a number of pseudopodia from the cell membrane, suggesting potential activation of human monocyte cells. In addition, the expression levels of pro‑inflammatory cytokines interleukin (IL)‑1β and tumor necrosis factor (TNF)‑α were also increased following treatment with Dex‑SPIONs. Simultaneously, the phosphorylation levels of mitogen‑activated protein kinase (MAPK) p38, c‑Jun N‑terminal kinase 1 and extracellular signal regulated kinase were markedly enhanced following nanoparticle exposure and MAPK inhibitors could abate the production of IL‑1β and TNF‑α. The results of the present study demonstrated that Dex‑SPIONs could activate human monocyte cells and that activation of MAPK pathway may be involved in these effects.
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Copy and paste a formatted citation
Spandidos Publications style
Wu Q, Miao T, Feng T, Yang C, Guo Y and Li H: Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells. Mol Med Rep 18: 564-570, 2018.
APA
Wu, Q., Miao, T., Feng, T., Yang, C., Guo, Y., & Li, H. (2018). Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells. Molecular Medicine Reports, 18, 564-570. https://doi.org/10.3892/mmr.2018.8972
MLA
Wu, Q., Miao, T., Feng, T., Yang, C., Guo, Y., Li, H."Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells". Molecular Medicine Reports 18.1 (2018): 564-570.
Chicago
Wu, Q., Miao, T., Feng, T., Yang, C., Guo, Y., Li, H."Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells". Molecular Medicine Reports 18, no. 1 (2018): 564-570. https://doi.org/10.3892/mmr.2018.8972
Copy and paste a formatted citation
x
Spandidos Publications style
Wu Q, Miao T, Feng T, Yang C, Guo Y and Li H: Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells. Mol Med Rep 18: 564-570, 2018.
APA
Wu, Q., Miao, T., Feng, T., Yang, C., Guo, Y., & Li, H. (2018). Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells. Molecular Medicine Reports, 18, 564-570. https://doi.org/10.3892/mmr.2018.8972
MLA
Wu, Q., Miao, T., Feng, T., Yang, C., Guo, Y., Li, H."Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells". Molecular Medicine Reports 18.1 (2018): 564-570.
Chicago
Wu, Q., Miao, T., Feng, T., Yang, C., Guo, Y., Li, H."Dextran‑coated superparamagnetic iron oxide nanoparticles activate the MAPK pathway in human primary monocyte cells". Molecular Medicine Reports 18, no. 1 (2018): 564-570. https://doi.org/10.3892/mmr.2018.8972
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