Desynchronization of the molecular clock contributes to the heterogeneity of the inflammatory response

Sci Signal. 2019 Mar 5;12(571):eaau1851. doi: 10.1126/scisignal.aau1851.

Abstract

Heterogeneity in the behavior of genetically and developmentally equivalent cells is becoming increasingly appreciated. There are several sources of cellular heterogeneity, including both intrinsic and extrinsic noise. We found that some aspects of heterogeneity in the response of macrophages to bacterial lipopolysaccharide (LPS) were due to intercellular desynchronization of the molecular clock, a cell-intrinsic oscillator. We found that the ratio of the relative expression of two clock genes, Nfil3 and Dbp, expressed in opposite phases of the clock, determined the fraction of cells that produced the cytokine IL-12p40 in response to LPS. The clock can be entrained by various environmental stimuli, making it a mechanism by which population-level heterogeneity and the inflammatory response can be regulated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Basic-Leucine Zipper Transcription Factors / immunology
  • Biological Clocks / drug effects*
  • Biological Clocks / genetics
  • Biological Clocks / immunology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • Interleukin-12 Subunit p40 / genetics
  • Interleukin-12 Subunit p40 / immunology
  • Lipopolysaccharides / toxicity*
  • Macrophages / immunology*
  • Macrophages / pathology
  • Mice
  • Mice, Transgenic
  • Transcription Factors / genetics
  • Transcription Factors / immunology

Substances

  • Basic-Leucine Zipper Transcription Factors
  • DNA-Binding Proteins
  • Dbp protein, mouse
  • Il12b protein, mouse
  • Interleukin-12 Subunit p40
  • Lipopolysaccharides
  • Nfil3 protein, mouse
  • Transcription Factors