Nuclear migration of NF-kappa B correlates with TNF-alpha mRNA accumulation

J Inflamm. 1995;45(1):64-71.

Abstract

Previous work on the transcriptional regulation of the mouse TNF-alpha promoter had indicated a major role for the NF-kappa B transcription factor in the induction of the gene by endotoxin. However, similar studies using the human promoter failed to establish a role for this factor. We measured the nuclear migration of NF-kappa B and the accumulation of TNF-alpha mRNA in murine T lymphoblasts and bone marrow-derived macrophages (BMDM) under different activation conditions, seeking to establish a correlation. Activation of NF-kappa B and accumulation of TNF-alpha mRNA correlated semiquantitatively under the following conditions: (1) inhibition of NF-kappa B by dithiocarbamates; (2) induction of TNF synthesis by taxol; (3) partial induction of TNF-alpha mRNA by various inducers in macrophages from lpsd mice; and (4) inhibition of NF-kappa B activation by a protease inhibitor. However, inhibition of TNF-alpha mRNA accumulation by cAMP inducers had no effect on NF-kappa B induction. We conclude that NF-kappa B translocation is necessary, but not sufficient for the transcriptional induction of the TNF-alpha gene by LPS in macrophages or by phorbol ester and ionomycin in T lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Biological Transport
  • Bone Marrow Cells
  • Cell Nucleus / metabolism*
  • Cells, Cultured
  • Cyclic AMP / metabolism
  • Free Radical Scavengers / pharmacology
  • Macrophages / metabolism
  • Macrophages / ultrastructure
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • NF-kappa B / metabolism*
  • Nocodazole / pharmacology
  • Paclitaxel / pharmacology
  • RNA, Messenger / metabolism*
  • Serine Proteinase Inhibitors / pharmacology
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / ultrastructure
  • Tosylphenylalanyl Chloromethyl Ketone / pharmacology
  • Tumor Necrosis Factor-alpha / genetics*

Substances

  • Free Radical Scavengers
  • NF-kappa B
  • RNA, Messenger
  • Serine Proteinase Inhibitors
  • Tumor Necrosis Factor-alpha
  • Tosylphenylalanyl Chloromethyl Ketone
  • Cyclic AMP
  • Paclitaxel
  • Nocodazole