Transcriptional repression in macrophages-basic mechanisms and alterations in metabolic inflammatory diseases

FEBS Lett. 2017 Oct;591(19):2959-2977. doi: 10.1002/1873-3468.12850. Epub 2017 Sep 25.

Abstract

Macrophage differentiation and signal responses are coordinated by closely linked transcriptional and epigenomic mechanisms that trigger gene expression. In contrast to well-characterized transcriptional activation pathways in response to diverse metabolic and inflammatory signals, we just begin appreciating that transcriptional repression is equally important. Here, we will highlight macrophage pathways that are controlled by multifaceted repression events, along with a discussion of underlying regulatory mechanisms and components. We will particularly discuss pro- versus anti-inflammatory action of a fundamental corepressor complex, transcription factor cross-talk, repression at enhancers and during elongation, and diverse corepressor knockout mouse models. We will finally emphasize how alterations of macrophage repression pathways in humans contribute to, or even cause, metabolic inflammatory diseases such as obesity and type 2 diabetes.

Keywords: corepressor; epigenome; macrophage; metaflammation; repression; transcription.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enhancer Elements, Genetic / genetics
  • Humans
  • Inflammation / complications
  • Inflammation / genetics*
  • Inflammation / pathology
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Metabolic Diseases / complications
  • Metabolic Diseases / genetics*
  • Metabolic Diseases / pathology
  • Signal Transduction / genetics
  • Transcription, Genetic*