Reduction of CD19 autoimmunity marker on B cells of paediatric SLE patients through repressing PU.1/TNF-α/BAFF axis pathway by miR-155

Growth Factors. 2017 Jun;35(2-3):49-60. doi: 10.1080/08977194.2017.1345900. Epub 2017 Jul 7.

Abstract

microRNA-155 (miR-155) is implicated in regulating B-cell activation and survival that is important in systemic lupus erythematosus (SLE) pathogenesis. PU.1, a target for miR-155, is a crucial regulator of B-cell development and enhances Tumour-Necrosis-factor-alpha (TNF-α) expression. TNF-α induces the expression of B-cell-activating-factor (BAFF). BAFF is reported to increase the expression of the autoimmunity marker; CD19. This study aimed to investigate the regulation of expression of PU.1 in pediatric-systemic-lupus-erythematosus (pSLE) patients by miR-155, and hence evaluate its impact on TNF-α/BAFF/CD19 signalling pathway. Screening revealed that PU.1 is upregulated in PBMCs and B-cells of pSLE patients. PU.1 expression directly correlated with systemic-lupus-erythematosus disease-activity-index-2 K SLEDAI-2K. Ectopic expression of miR-155 and knockdown of PU.1 suppressed PU.1, TNF-α and BAFF. Finally, miR-155 decreased the proportion of BAFF-expressing-B-cells and CD19 protein expression. These findings suggest that miR-155 suppresses autoimmunity through transcriptional repression of PU.1 and TNF-α, which in turn suppresses BAFF and CD19 protein expression.

Keywords: B cells; BAFF; PU.1; TNF-α; lupus; microRNA 155.

MeSH terms

  • Antigens, CD19 / blood*
  • Autoimmunity*
  • B-Cell Activating Factor / genetics
  • B-Cell Activating Factor / metabolism
  • B-Lymphocytes / immunology*
  • Biomarkers / blood
  • Cells, Cultured
  • Child
  • Female
  • Humans
  • Lupus Erythematosus, Systemic / blood
  • Lupus Erythematosus, Systemic / immunology*
  • Male
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Monocytes / immunology
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Signal Transduction
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antigens, CD19
  • B-Cell Activating Factor
  • Biomarkers
  • MIRN155 microRNA, human
  • MicroRNAs
  • Proto-Oncogene Proteins
  • TNFSF13B protein, human
  • Trans-Activators
  • Tumor Necrosis Factor-alpha
  • proto-oncogene protein Spi-1