JQ1, a BET inhibitor, controls TLR4-induced IL-10 production in regulatory B cells by BRD4-NF-κB axis. Article uri icon

Overview

abstract

  • Regulatory B cells, also well-known as IL-10-producing B cells, play a role in the suppression of inflammatory responses. However, the epigenetic modulation of regulatory B cells is largely unknown. Recent studies showed that the bromodomain and extra-terminal domain (BET) protein inhibitor JQ1 controls the expression of various genes involving cell proliferation and cell cycle. However, the role of BET proteins on development of regulatory B cells is not reported. In this study, JQ1 potently suppressed IL-10 expression and secretion in murine splenic and peritoneal B cells. While bromodomaincontaining protein 4 (BRD4) was associated with NF-κB on IL-10 promoter region by LPS stimulation, JQ1 interfered the interaction of BRD4 with NF-κB on IL-10 promoter. In summary, BRD4 is essential for toll like receptor 4 (TLR4)-mediated IL-10 expression, suggesting JQ1 could be a potential candidate in regulating IL-10-producing regulatory B cells in cancer. [BMB Reports 2017; 50(12): 640-646].

publication date

  • December 1, 2017

Research

keywords

  • Azepines
  • B-Lymphocytes, Regulatory
  • Interleukin-10
  • NF-kappa B
  • Nuclear Proteins
  • Toll-Like Receptor 4
  • Transcription Factors
  • Triazoles

Identity

PubMed Central ID

  • PMC5749911

Scopus Document Identifier

  • 85040078572

Digital Object Identifier (DOI)

  • 10.5483/bmbrep.2017.50.12.194

PubMed ID

  • 29187284

Additional Document Info

volume

  • 50

issue

  • 12