Immunological function of Blimp-1 in dendritic cells and relevance to autoimmune diseases

Immunol Res. 2015 Dec;63(1-3):113-20. doi: 10.1007/s12026-015-8694-5.

Abstract

Previous studies have identified the immunological functions of transcription factor B lymphocyte-induced maturation protein-1 (Blimp-1) in various adaptive immune cell types such as T and B lymphocytes. More recently, it has been shown that Blimp-1 extends its functional roles to dendritic cells (DCs) and macrophages, two cell types belonging to the innate immune system. The protein acts as a direct and indirect regulator of target genes by recruiting chromatin modification factors and by regulating microRNA expression, respectively. In DCs, Blimp-1 has been identified as one of the components involved in antigen presentation. Genome-wide association studies identified polymorphisms associated with multiple autoimmune diseases such as system lupus erythematosus, rheumatoid arthritis, and inflammatory bowel disease in PRDM1, the gene encoding Blimp-1 protein. In this review, we will discuss the immune regulatory functions of Blimp-1 in DCs with a main focus on the tolerogenic mechanisms of Blimp-1 required to protect against the development of autoimmune diseases.

Keywords: Antigen presentation; Blimp-1; Dendritic cells; SLE.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Antigen Presentation
  • Autoimmune Diseases / immunology*
  • Dendritic Cells / immunology*
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Humans
  • Immune Tolerance
  • Immunity
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Polymorphism, Genetic
  • Positive Regulatory Domain I-Binding Factor 1
  • Repressor Proteins / genetics
  • Repressor Proteins / immunology
  • Repressor Proteins / metabolism*

Substances

  • MicroRNAs
  • Repressor Proteins
  • PRDM1 protein, human
  • Positive Regulatory Domain I-Binding Factor 1