L-selectin signaling of neutrophil adhesion and degranulation involves p38 mitogen-activated protein kinase

J Biol Chem. 2000 May 26;275(21):15876-84. doi: 10.1074/jbc.M906232199.

Abstract

The adhesion molecules known as selectins mediate the capture of neutrophils from the bloodstream. We have previously reported that ligation and cross-linking of L-selectin on the neutrophil surface enhances the adhesive function of beta(2)-integrins in a synergistic manner with chemotactic agonists. In this work, we examined degranulation and adhesion of neutrophils in response to cross-linking of L-selectin and addition of interleukin-8. Cross-linking of L-selectin induced priming of degranulation that was similar to that observed with the alkaloid cytochalasin B. Activation mediated by L-selectin of neutrophil shape change and adhesion through CD11b/CD18 were strongly blocked by Merck C, an imidazole-based inhibitor of p38 mitogen-activated protein kinase (MAPK), but not by a structurally similar non-binding regioisomer. Priming by L-selectin of the release of secondary, tertiary, and secretory, but not primary, granules was blocked by inhibition of p38 MAPK. Peak phosphorylation of p38 MAPK was observed within 1 min of cross-linking L-selectin, whereas phosphorylation of ERK1/2 was highest at 10 min. Phosphorylation of p38 MAPK, but not ERK1/2, was inhibited by Merck C. These data suggest that signal transduction as a result of clustering L-selectin utilizes p38 MAPK to effect neutrophil shape change, integrin activation, and the release of secondary, tertiary, and secretory granules.

Publication types

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

MeSH terms

  • Cell Adhesion* / drug effects
  • Cell Size
  • Cross-Linking Reagents / metabolism
  • Cytoplasmic Granules / drug effects
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Interleukin-8 / metabolism
  • Kinetics
  • L-Selectin / metabolism*
  • Macrophage-1 Antigen / metabolism
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neutrophil Activation*
  • Neutrophils / drug effects
  • Neutrophils / metabolism*
  • Phosphorylation
  • Signal Transduction*
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Cross-Linking Reagents
  • Enzyme Inhibitors
  • Interleukin-8
  • Macrophage-1 Antigen
  • L-Selectin
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases