5-lipoxygenase is phosphorylated by p38 kinase-dependent MAPKAP kinases

Proc Natl Acad Sci U S A. 2000 May 9;97(10):5261-6. doi: 10.1073/pnas.050588997.

Abstract

5-lipoxygenase (5-LO) catalyzes the initial steps in the formation of leukotrienes, a group of inflammatory mediators derived from arachidonic acid (AA). Here we describe that activation of p38 mitogen-activated protein kinase in human polymorphonuclear leukocytes and in Mono Mac 6 cells leads to activation of downstream kinases, which can subsequently phosphorylate 5-LO in vitro. Different agents activated the 5-LO kinase activities, including stimuli for cellular leukotriene biosynthesis (A23187, thapsigargin, N-formyl-leucyl-phenylalanine), compounds that up-regulate the capacity for leukotriene biosynthesis (phorbol 12-myristate 13-acetate, tumor necrosis factor alpha, granulocyte/macrophage colony-stimulating factor), and well known p38 stimuli as sodium arsenite and sorbitol. For all stimuli, 5-LO kinase activation was counteracted by SB203580 (3 microM or less), an inhibitor of p38 kinase. At least two p38-dependent 5-LO kinase activities were found. Based on migration properties in in-gel kinase assays and immunoreactivity, one of these was identified as mitogen-activated protein kinase-activated protein kinase 2 (MAPKAP kinase 2). The other appeared to be MAPKAP kinase 3; however, it could not be excluded that also other p38-dependent kinases contributed. When polymorphonuclear leukocytes were incubated with sodium arsenite (strong activator of 5-LO kinases), platelet-activating factor and exogenous AA, there was a 4-fold increase in 5-LO activity as compared with incubations with only platelet-activating factor and AA. This indicates that 5-LO phosphorylation can be one factor determining cellular 5-LO activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Arachidonate 5-Lipoxygenase / chemistry
  • Arachidonate 5-Lipoxygenase / metabolism*
  • Arsenites / pharmacology
  • Calcimycin / pharmacology
  • Cell Line
  • Cricetinae
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Kinetics
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism*
  • N-Formylmethionine Leucyl-Phenylalanine / pharmacology
  • Neutrophils / drug effects
  • Neutrophils / enzymology*
  • Neutrophils / physiology
  • Phosphorylation
  • Protein Serine-Threonine Kinases / metabolism*
  • Rats
  • Recombinant Proteins / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Sodium Compounds / pharmacology
  • Tetradecanoylphorbol Acetate / pharmacology
  • Thapsigargin / pharmacology
  • Tumor Necrosis Factor-alpha / pharmacology
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Arsenites
  • Intracellular Signaling Peptides and Proteins
  • Recombinant Proteins
  • Sodium Compounds
  • Tumor Necrosis Factor-alpha
  • Calcimycin
  • sodium arsenite
  • N-Formylmethionine Leucyl-Phenylalanine
  • Thapsigargin
  • Arachidonate 5-Lipoxygenase
  • MAP-kinase-activated kinase 2
  • MAP-kinase-activated kinase 3
  • Protein Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Tetradecanoylphorbol Acetate