IL-1 beta transcript stability in monocytes is linked to cytoskeletal reorganization and the availability of mRNA degradation factors

Immunol Cell Biol. 2002 Aug;80(4):328-39. doi: 10.1046/j.1440-1711.2002.01085.x.

Abstract

Monocyte extravasation initiates reorganization of the cytoskeleton (CSK) and adhesion-dependent cytokine gene transcription. The actin CSK is thought to be crucial for compartmentalization and translation of mRNA, many of which contain AU-rich (ARE) instability motifs in the 3' untranslated region. We investigated regulation of adhesion-induced IL-1 beta expression by the monocyte CSK. In serum-free adherent monocytes, the induced IL-1 beta mRNA was stable and did not coextract with actin filaments. In contrast, in cells adherent in autologous serum, IL-1 beta transcripts were unstable, coextracted with actin filaments and were associated with only transient activation of the mitogen-activated protein kinases (MAPK). Under both conditions of adherence, the ARE-binding protein AUF1/hnRNP D was readily extracted in the cytosolic fraction. Electro-injection with AUF1/hnRNP D modified the actin CSK and, surprisingly, stabilized IL-1 beta transcripts. These data suggest that the control of mRNA degradation is linked with changes in the CSK. Mitogen-activated protein kinase activation or alterations in the availability of mRNA degradation factors may mediate these effects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actin Cytoskeleton / chemistry
  • Actin Cytoskeleton / ultrastructure*
  • Cell Adhesion
  • Cells, Cultured
  • Culture Media
  • Cytoskeletal Proteins / analysis
  • Heterogeneous Nuclear Ribonucleoprotein D0
  • Heterogeneous-Nuclear Ribonucleoprotein D / analysis
  • Humans
  • Interleukin-1 / genetics*
  • Interleukin-1 / metabolism
  • Intermediate Filaments / chemistry
  • Kinetics
  • Mitogen-Activated Protein Kinases / metabolism
  • Monocytes / immunology*
  • Monocytes / ultrastructure*
  • RNA Stability*
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / analysis
  • Signal Transduction
  • Transcription, Genetic

Substances

  • Culture Media
  • Cytoskeletal Proteins
  • HNRNPD protein, human
  • Heterogeneous Nuclear Ribonucleoprotein D0
  • Heterogeneous-Nuclear Ribonucleoprotein D
  • Interleukin-1
  • RNA, Messenger
  • RNA-Binding Proteins
  • Mitogen-Activated Protein Kinases