Constitutive Interferon Attenuates RIPK1/3-Mediated Cytokine Translation

Cell Rep. 2020 Jan 21;30(3):699-713.e4. doi: 10.1016/j.celrep.2019.12.073.

Abstract

Receptor-interacting protein kinase 1 (RIPK1) and 3 (RIPK3) are well known for their capacity to drive necroptosis via mixed-lineage kinase-like domain (MLKL). Recently, RIPK1/3 kinase activity has been shown to drive inflammation via activation of MAPK signaling. However, the regulatory mechanisms underlying this kinase-dependent cytokine production remain poorly understood. In the present study, we establish that the kinase activity of RIPK1/3 regulates cytokine translation in mouse and human macrophages. Furthermore, we show that this inflammatory response is downregulated by type I interferon (IFN) signaling, independent of type I IFN-promoted cell death. Specifically, low-level constitutive IFN signaling attenuates RIPK-driven activation of cap-dependent translation initiation pathway components AKT, mTORC1, 4E-BP and eIF4E, while promoting RIPK-dependent cell death. Altogether, these data characterize constitutive IFN signaling as a regulator of RIPK-dependent inflammation and establish cap-dependent translation as a crucial checkpoint in the regulation of cytokine production.

Keywords: constitutive IFN; inflammation; macrophage; necroptosis; receptor-interacting protein kinases; translation.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Cell Cycle Proteins / metabolism
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Down-Regulation
  • Eukaryotic Initiation Factor-4E / metabolism
  • Female
  • Humans
  • Inflammation / pathology
  • Interferons / metabolism*
  • Lipopolysaccharides / pharmacology
  • Macrophage Activation / drug effects
  • Mechanistic Target of Rapamycin Complex 1 / metabolism
  • Mice, Inbred C57BL
  • Protein Biosynthesis*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction

Substances

  • Adaptor Proteins, Signal Transducing
  • Cell Cycle Proteins
  • Cytokines
  • Eif4ebp1 protein, mouse
  • Eukaryotic Initiation Factor-4E
  • Lipopolysaccharides
  • RNA, Messenger
  • Interferons
  • Mechanistic Target of Rapamycin Complex 1
  • RIPK1 protein, human
  • RIPK3 protein, human
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Ripk1 protein, mouse
  • Ripk3 protein, mouse