RIG-I plays a critical role in negatively regulating granulocytic proliferation

Proc Natl Acad Sci U S A. 2008 Jul 29;105(30):10553-8. doi: 10.1073/pnas.0804895105. Epub 2008 Jul 23.

Abstract

RIG-I has been implicated in innate immunity by sensing intracellular viral RNAs and inducing type I IFN production. However, we have found a significant RIG-I induction in a biological setting without active viral infection-namely, during RA-induced terminal granulocytic differentiation of acute myeloid leukemias. Here, we present evidence that a significant Rig-I induction also occurs during normal myelopoiesis and that the disruption of the Rig-I gene in mice leads to the development of a progressive myeloproliferative disorder. The initiation of progressive myeloproliferative disorder is mainly due to an intrinsic defect of Rig-I(-/-) myeloid cells, which are characterized by a reduced expression of IFN consensus sequence binding protein, a major regulator of myeloid differentiation. Thus, our study reveals a critical regulatory role of Rig-I in modulating the generation and differentiation of granulocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Proliferation
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / physiology*
  • Exons
  • Gene Expression Regulation*
  • Granulocytes / cytology*
  • Granulocytes / metabolism
  • Hematopoietic Stem Cells / cytology
  • Humans
  • Immunity, Innate
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Myeloid Cells / cytology
  • Myeloproliferative Disorders / metabolism
  • Receptors, Retinoic Acid / physiology*

Substances

  • PLAAT4 protein, human
  • Receptors, Retinoic Acid
  • Ddx58 protein, mouse
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases