Downregulation of microRNA-155-5p prevents immune thrombocytopenia by promoting macrophage M2 polarization via the SOCS1-dependent PD1/PDL1 pathway

Life Sci. 2020 Sep 15:257:118057. doi: 10.1016/j.lfs.2020.118057. Epub 2020 Jul 4.

Abstract

Aims: We set about to investigate the potential role of microRNA-155-5p (miR-155-5p) in the development of immune thrombocytopenia (ITP), an idiopathic deficiency of blood platelets.

Main methods: Initially, RT-qPCR and Western blot analyses were carried out to determine the expression of miR-155-5p and SOCS1 in peripheral blood mononuclear cells (PBMCs) and macrophages from ITP patients. We undertook gain- and loss- function methods by transfection of macrophages and PBMCs with treated plasmids. The expression patterns of platelet-related factors were measured by ELISA, and the expressions of PD1, PDL1, and macrophage M2 marker CD206 and CD86 were also measured. The relationship between miR-155-5p and SOCS1 was determined using the dual-luciferase reporter gene assay. We also established an ITP mouse model to explore the roles of miR-155-5p and SOCS1 in vivo.

Key findings: miR-155-5p was up-regulated, while SOCS1 was down-regulated in PBMCs and macrophages from ITP patients. SOCS1 was indicated as a target of miR-155-5p. Inhibition of miR-155-5p or up-regulation of SOCS1 facilitated macrophage M2 polarization as demonstrated by an increased M2/M1 ratio and suppressed expression of platelet-related factors. Furthermore, silencing of SOCS1 promoted ITP progression through blocking the PD1/PDL1 pathway, whilst upregulation of miR-155-5p remarkably increased the platelet abundance and suppressed SOCS1 expression in ITP model mice.

Significance: Silencing of miR-155-5p could promote PD1/PDL1 pathway-mediated macrophage M2 polarization and prevent ITP via up-regulation of SOCS1, thus relieving ITP.

Keywords: Immune thrombocytopenia; Macrophage M2 polarization; Peripheral blood mononuclear cell; SOCS1; microRNA-155-5p.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • B7-H1 Antigen / metabolism
  • Disease Progression
  • Down-Regulation
  • Female
  • Gene Silencing
  • Humans
  • Leukocytes, Mononuclear / metabolism
  • Macrophages / metabolism*
  • Male
  • Mice
  • Mice, Inbred CBA
  • MicroRNAs / genetics*
  • Middle Aged
  • Programmed Cell Death 1 Receptor / metabolism
  • Purpura, Thrombocytopenic, Idiopathic / genetics*
  • Purpura, Thrombocytopenic, Idiopathic / physiopathology
  • Suppressor of Cytokine Signaling 1 Protein / genetics*
  • Up-Regulation
  • Young Adult

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • MIRN155 microRNA, human
  • MicroRNAs
  • Mirn155 microRNA, mouse
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • SOCS1 protein, human
  • Socs1 protein, mouse
  • Suppressor of Cytokine Signaling 1 Protein