Lipopolysaccharide-induced NF-kappa B activation in mouse 70Z/3 pre-B lymphocytes is inhibited by mevinolin and 5'-methylthioadenosine: roles of protein isoprenylation and carboxyl methylation reactions

Mol Cell Biol. 1992 Jan;12(1):103-11. doi: 10.1128/mcb.12.1.103-111.1992.

Abstract

We show that both the lipopolysaccharide (LPS)-induced activation of NF-kappa DNA binding and kappa gene expression are blocked by treating murine pre-B lymphocyte 70Z/3 cells with 5'-methylthioadenosine (MTA), an inhibitor of several S-adenosylmethionine-dependent methylation reactions. We further show that the LPS-induced incorporation of radioactivity from [methyl-3H]methionine into methyl ester-like linkages on a group of membrane polypeptides is also inhibited by MTA treatment, suggesting the involvement of protein methylation reactions in the LPS signal transduction pathway. We also find that NF-kappa B and kappa gene activation in LPS-treated 70Z/3 cells is blocked by mevinolin, an inhibitor that prevents protein isoprenylation. Interestingly, mevinolin-treated cells also exhibited a marked reduction in the methylation of membrane proteins. Neither MTA nor mevinolin significantly inhibited NF-kappa B activation by phorbol myristate acetate, suggesting that these agents act early in signal transduction. These results provide the first evidence that carboxyl methylated and/or isoprenylated proteins play an essential role in the LPS-signaling pathway.

Publication types

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

MeSH terms

  • Adenosine / analogs & derivatives*
  • Adenosine / pharmacology
  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism*
  • Clone Cells
  • Deoxyadenosines*
  • Electrophoresis, Polyacrylamide Gel
  • Gene Expression Regulation* / drug effects
  • Immunoglobulin kappa-Chains / genetics
  • Immunoglobulin kappa-Chains / metabolism
  • Lipopolysaccharides*
  • Lovastatin / pharmacology*
  • Membrane Proteins / metabolism
  • Methylation
  • NF-kappa B / metabolism*
  • Protein Biosynthesis
  • Signal Transduction
  • Thionucleosides / pharmacology*
  • Transcriptional Activation

Substances

  • Deoxyadenosines
  • Immunoglobulin kappa-Chains
  • Lipopolysaccharides
  • Membrane Proteins
  • NF-kappa B
  • Thionucleosides
  • 5'-methylthioadenosine
  • Lovastatin
  • Adenosine