Interaction of AU-rich sequence binding proteins with actin: possible involvement of the actin cytoskeleton in lymphokine mRNA turnover

J Cell Physiol. 1997 Oct;173(1):19-27. doi: 10.1002/(SICI)1097-4652(199710)173:1<19::AID-JCP3>3.0.CO;2-M.

Abstract

In the current study, we report that cytochalasin-induced disruption of microfilaments stabilizes lymphokine mRNAs in activated human peripheral blood lymphocytes. Parallel with this, a dose- and time-dependent increase in AU-rich sequence binding protein (AUPB) activities is apparent in the nonionic detergent-resistant fractions of these cells, suggesting that cytochalasin-induced modulation of lymphokine mRNA stability might be mediated through cytoplasmic AUBPs. We provide evidence that some of the AUBPs can be immunoprecipitated with anti-actin antibodies, implicating the potential of these proteins to associate with the actin-based cytoskeleton in vivo. Moreover, disruption of the microfilament network by cytochalasins produces increased immunoprecipitable actin-AUBP complexes in the detergent-resistant cytoplasmic subfractions of lymphocytes. We show that cytochalasin-induced changes in AUBP activities are parallel with their higher binding affinity to RNA containing AU-rich instability sequence element as judged by in vitro competition and in vivo ultraviolet-crosslinking analysis. Correlation of these findings with changes in mRNA stability indicates that the actin cytoskeleton may play a physiologically important role in posttranscriptional regulation of lymphokine gene expression during early lymphocyte activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / drug effects
  • Actin Cytoskeleton / metabolism*
  • Actins / immunology
  • Actins / metabolism*
  • Blotting, Northern
  • Cytochalasins / pharmacology
  • Dactinomycin / pharmacology
  • Gene Expression Regulation
  • Humans
  • Interleukin-2 / genetics
  • Lymphocyte Activation
  • Lymphocytes / metabolism*
  • Lymphokines / genetics*
  • Lymphokines / metabolism
  • Octoxynol / pharmacology
  • Phytohemagglutinins / pharmacology
  • Precipitin Tests
  • RNA Probes
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / immunology
  • RNA-Binding Proteins / metabolism*
  • Tumor Necrosis Factor-alpha / genetics
  • Ultraviolet Rays

Substances

  • Actins
  • Cytochalasins
  • Interleukin-2
  • Lymphokines
  • Phytohemagglutinins
  • RNA Probes
  • RNA, Messenger
  • RNA-Binding Proteins
  • Tumor Necrosis Factor-alpha
  • Dactinomycin
  • Octoxynol