Tantalum Particles Induced Cytotoxic and Inflammatory Effects in Human Monocytes

Biomed Res Int. 2021 Jan 29:2021:6658498. doi: 10.1155/2021/6658498. eCollection 2021.

Abstract

The aim of this study is to evaluate the biological safety of tantalum (Ta) particles and to further explore the effects of Ta particles on human monocyte toxicity and inflammatory cytokine expression. Human monocyte leukemia (THP-1) cells were cultured with Ta and hydroxyapatite (HA) particles. Cell counting kit-8 method was used to evaluate the cytotoxicity of Ta and HA particles. The apoptosis effects were evaluated by flow cytometry, and the protein expression levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) were evaluated by ELISA. The protein levels of inflammation-related signaling pathways including nuclear factor-kappa B (NF-κB) and extracellular regulated kinase (ERK) were detected by western blotting. The cytotoxicity test showed that the toxicity level of Ta in vitro was grade l, which is within the clinically acceptable range. Compared with the HA control, Ta had no significant effect on THP-1 cell apoptosis, IL-6, and TNF-α release. The phosphorylated levels of NF-κB and ERK at 3 h in the Ta group were lower than those in the HA and control groups (P < 0.001 both). These results reveal Ta particles behave good biosafety properties and provide some new insights for the future clinical use of Ta.

MeSH terms

  • Cytokines / genetics
  • Gene Expression Regulation / drug effects
  • Humans
  • Inflammation / chemically induced
  • Inflammation / genetics
  • Inflammation / pathology
  • Interleukin-6 / genetics*
  • MAP Kinase Signaling System / drug effects
  • Mitogen-Activated Protein Kinases / genetics
  • Monocytes / drug effects*
  • Monocytes / pathology
  • NF-kappa B / genetics*
  • Phosphorylation / drug effects
  • Signal Transduction / drug effects
  • THP-1 Cells
  • Tantalum / pharmacology*
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Cytokines
  • Interleukin-6
  • NF-kappa B
  • Tumor Necrosis Factor-alpha
  • Tantalum
  • Mitogen-Activated Protein Kinases