Counter Regulation of Spic by NF-κB and STAT Signaling Controls Inflammation and Iron Metabolism in Macrophages

Cell Rep. 2020 Jun 30;31(13):107825. doi: 10.1016/j.celrep.2020.107825.

Abstract

Activated macrophages must carefully calibrate their inflammatory responses to balance efficient pathogen control with inflammation-mediated tissue damage, but the molecular underpinnings of this "balancing act" remain unclear. Using genetically engineered mouse models and primary macrophage cultures, we show that Toll-like receptor (TLR) signaling induces the expression of the transcription factor Spic selectively in patrolling monocytes and tissue macrophages by a nuclear factor κB (NF-κB)-dependent mechanism. Functionally, Spic downregulates pro-inflammatory cytokines and promotes iron efflux by regulating ferroportin expression in activated macrophages. Notably, interferon-gamma blocks Spic expression in a STAT1-dependent manner. High levels of interferon-gamma are indicative of ongoing infection, and in its absence, activated macrophages appear to engage a "default" Spic-dependent anti-inflammatory pathway. We also provide evidence for the engagement of this pathway in sterile inflammation. Taken together, our findings uncover a pathway wherein counter-regulation of Spic by NF-κB and STATs attune inflammatory responses and iron metabolism in macrophages.

Keywords: Bach1; NF-κB; Spic; ferroportin; interferon-gamma; macrophages; monocytes.

Publication types

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

MeSH terms

  • Animals
  • Biological Transport
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation / genetics
  • Female
  • Heme / metabolism
  • Inflammation / metabolism*
  • Inflammation / pathology*
  • Interferon-gamma / metabolism
  • Iron / metabolism*
  • Ligands
  • Macrophage Activation
  • Macrophages / metabolism*
  • Male
  • Mice, Inbred C57BL
  • Monocytes / metabolism
  • NF-kappa B / metabolism*
  • STAT Transcription Factors / metabolism*
  • Signal Transduction*
  • Toll-Like Receptors / metabolism

Substances

  • DNA-Binding Proteins
  • Ligands
  • NF-kappa B
  • STAT Transcription Factors
  • Spic protein, mouse
  • Toll-Like Receptors
  • Heme
  • Interferon-gamma
  • Iron