The Toxoplasma gondii ME-49 strain upregulates levels of A20 that inhibit NF-κB activation and promotes apoptosis in human leukaemia T-cell lines

Parasit Vectors. 2018 May 18;11(1):305. doi: 10.1186/s13071-018-2837-1.

Abstract

Background: Acute T-lymphocyte leukaemia is a form of haematological malignancy with abnormal activation of NF-κB pathway, which results in high expression of A20 and ABIN1, which constitute a negative feedback mechanism for the regulation of NF-κB activation. Clinical studies have found that acute T-lymphocyte leukaemia patients are susceptible to Toxoplasma gondii infection; however, the effect of T. gondii on the proliferation and apoptosis of human leukaemia T-cells remains unclear. Here, we used the T. gondii ME-49 strain to infect human leukaemia T-cell lines Jurkat and Molt-4, to explore the effect of T. gondii on proliferation and apoptosis, which is mediated by NF-κB in human leukaemia T-cells.

Methods: The Tunel assay was used to detect cell apoptosis. Cell Counting Kit-8 was used to detect cell proliferation viability. The apoptosis level and the expression level of NF-κB related proteins in human leukaemia T-cells were detected by flow cytometry and Western blotting.

Results: Western blotting analyses revealed that the T. gondii ME-49 strain increased the expression of A20 and decreased both ABIN1 expression and NF-κB p65 phosphorylation. By constructing a lentiviral-mediated shRNA to knockdown the A20 gene in Jurkat T-cells and Molt-4 T-cells, the apoptosis levels of the two cell lines decreased after T. gondii ME-49 infection, and levels of NF-κB p65 phosphorylation and ABIN1 were higher than in the non-konckdown group. After knockingdown ABIN1 gene expression by constructing the lentiviral-mediated shRNA and transfecting the recombinant expression plasmid containing the ABIN1 gene into two cell lines, apoptosis levels and cleaved caspase-8 expression increased or decreased in response to T. gondii ME-49 infection, respectively.

Conclusions: Our data suggest that ABIN1 protects human leukaemia T-cells by allowing them to resist the apoptosis induced by T. gondii ME-49 and that the T. gondii ME-49 strain induces the apoptosis of human leukaemia T-cells via A20-mediated downregulation of ABIN1 expression.

Keywords: A20; ABIN1; Apoptosis; Human leukaemia T-cells; Toxoplasma gondii ME-49 strain.

MeSH terms

  • Apoptosis*
  • Cell Proliferation
  • Cell Survival
  • DNA-Binding Proteins / genetics
  • Down-Regulation
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Humans
  • Jurkat Cells
  • NF-kappa B / metabolism*
  • Phosphorylation
  • Signal Transduction / genetics
  • T-Lymphocytes / pathology*
  • Toxoplasma / genetics*
  • Tumor Necrosis Factor alpha-Induced Protein 3 / deficiency
  • Tumor Necrosis Factor alpha-Induced Protein 3 / genetics*
  • Up-Regulation

Substances

  • DNA-Binding Proteins
  • NF-kappa B
  • TNIP1 protein, human
  • TNFAIP3 protein, human
  • Tumor Necrosis Factor alpha-Induced Protein 3