DEC1/STRA13 is a key negative regulator of activation-induced proliferation of human B cells highly expressed in anergic cells

Immunol Lett. 2018 Jun:198:7-11. doi: 10.1016/j.imlet.2018.03.014. Epub 2018 Mar 29.

Abstract

The transcription factor DEC1/STRA13 (also known as BHLHE40 and SHARP2) is involved in a number of processes including inhibition of cell proliferation and delay of cell cycle, and is a negative regulator of B cell activation and development in mice. We show here that, unlike in mice, DEC1/STRA13 expression is induced in human naïve and memory resting B cells by activation through the B-cell receptor (BCR) or Toll-like receptor 9 (TLR9). siRNA silencing of DEC1/STRA13 increases the capacity of activated B cells to perform a high number of divisions after TLR9 ligation. This identifies DEC1/STRA13 as a critical negative regulator of clonal expansion of activated human B cells. We also show that DEC1/STRA13 is upregulated in human anergic CD21low B cells clonally expanded in patients with HCV-associated mixed cryoglobulinemia, which fail to proliferate in response to BCR or TLR9 ligation. siRNA knockdown of DEC1/STRA13, however, fails to restore responsiveness to stimuli in these cells, although it might improve the proliferative capacity in a subset of anergic cells with less pronounced proliferative defect.

Keywords: Activation; Anergy; B cells; Cryoglobulinemia; DEC1/STRA13; Proliferation; siRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / immunology*
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Cell Cycle
  • Cell Proliferation
  • Cells, Cultured
  • Clonal Anergy*
  • Cryoglobulinemia / genetics
  • Cryoglobulinemia / immunology
  • Cryoglobulinemia / pathology
  • Gene Expression Regulation / immunology
  • Gene Knockdown Techniques
  • Hepatitis C / genetics
  • Hepatitis C / immunology
  • Hepatitis C / pathology
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism*
  • Humans
  • Lymphocyte Activation*
  • RNA, Small Interfering / metabolism
  • Receptors, Antigen, B-Cell / metabolism
  • Signal Transduction
  • Toll-Like Receptor 9 / metabolism

Substances

  • BHLHE40 protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • Homeodomain Proteins
  • RNA, Small Interfering
  • Receptors, Antigen, B-Cell
  • TLR9 protein, human
  • Toll-Like Receptor 9