Mycobacterium tuberculosis and macrophage nuclear receptors: What we do and don't know

Tuberculosis (Edinb). 2019 May:116S:S98-S106. doi: 10.1016/j.tube.2019.04.016. Epub 2019 Apr 25.

Abstract

Nuclear receptors (NRs) are ligand-activated transcription factors that are expressed in a wide variety of cells and play a major role in lipid signaling. NRs are key regulators of immune and metabolic functions in macrophages and are linked to macrophage responses to microbial pathogens. Pathogens are also known to induce the expression of specific NRs to promote their own survival. In this review, we focus on the NRs recently shown to influence macrophage responses to Mycobacterium tuberculosis (M.tb), a significant cause of morbidity and mortality worldwide. We provide an overview of NR-controlled transcriptional activity and regulation of macrophage activation. We also discuss in detail the contribution of specific NRs to macrophage responses to M.tb, including influence on macrophage phenotype, cell signaling, and cellular metabolism. We pay particular attention to PPARγ since it is required for differentiation of alveolar macrophages, an important niche for M.tb, and its role during M.tb infection is becoming increasingly appreciated. Research into NRs and M.tb is still in its early stages, therefore continuing to advance our understanding of the complex interactions between M.tb and macrophage NRs may reveal the potential of NRs as pharmacological targets for the treatment of tuberculosis.

Keywords: Macrophage; Mycobacterium tuberculosis; Nuclear receptors; PPARγ.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Nucleus / metabolism*
  • Cell Nucleus / microbiology
  • Host-Pathogen Interactions
  • Humans
  • Macrophage Activation
  • Macrophages / metabolism*
  • Macrophages / microbiology
  • Mycobacterium tuberculosis / metabolism*
  • PPAR gamma / metabolism*
  • Signal Transduction
  • Tuberculosis / diagnosis
  • Tuberculosis / metabolism*
  • Tuberculosis / microbiology

Substances

  • PPAR gamma
  • PPARG protein, human