The peptidyl-prolyl isomerase Pin1 regulates the stability of granulocyte-macrophage colony-stimulating factor mRNA in activated eosinophils

Nat Immunol. 2005 Dec;6(12):1280-7. doi: 10.1038/ni1266. Epub 2005 Nov 6.

Abstract

The infiltration, accumulation and degranulation of eosinophils in the lung represents a hallmark of active asthma. In vivo or in vitro eosinophil activation triggers the secretion of the antiapoptotic cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF). We now identify Pin1, a cis-trans isomerase, as an essential component of the ribonucleoprotein complex responsible for GM-CSF mRNA stabilization, cytokine secretion and the survival of activated eosinophils. Pin1 regulated the association of the AU-rich element-binding proteins AUF1 and hnRNP C with GM-CSF mRNA, accelerating or slowing decay, respectively. These data indicate Pin1 is a key mediator of GM-CSF production.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Allergens / immunology
  • Cell Survival / physiology
  • Cells, Cultured
  • Eosinophils / enzymology*
  • Eosinophils / immunology
  • Granulocyte-Macrophage Colony-Stimulating Factor / biosynthesis
  • Granulocyte-Macrophage Colony-Stimulating Factor / genetics*
  • Heterogeneous Nuclear Ribonucleoprotein D0
  • Heterogeneous-Nuclear Ribonucleoprotein D / metabolism
  • Humans
  • Hyaluronic Acid / physiology
  • NIMA-Interacting Peptidylprolyl Isomerase
  • Peptidylprolyl Isomerase / physiology*
  • RNA Stability
  • RNA, Messenger / metabolism*

Substances

  • Allergens
  • HNRNPD protein, human
  • Heterogeneous Nuclear Ribonucleoprotein D0
  • Heterogeneous-Nuclear Ribonucleoprotein D
  • NIMA-Interacting Peptidylprolyl Isomerase
  • RNA, Messenger
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Hyaluronic Acid
  • PIN1 protein, human
  • Peptidylprolyl Isomerase