Maximal human neutrophil priming for superoxide production and elastase release requires p38 mitogen-activated protein kinase activation

Arch Surg. 2000 Feb;135(2):219-25. doi: 10.1001/archsurg.135.2.219.

Abstract

Hypothesis: Neutrophil priming has been implicated in the development of multiple organ failure, although the precise intracellular mechanisms that regulate neutrophil priming remain unclear. Our previous work characterized platelet-activating factor (PAF) priming of human neutrophils for concordant superoxide anion (O2-) generation and elastase degranulation. The p38 mitogen-activated protein kinase (MAPK) is activated by PAF stimulation. We hypothesized that PAF-induced human neutrophil priming for O2- and elastase release is mediated via the p38 MAPK pathway.

Design: Isolated neutrophils from 6 human donors were preincubated with the specific p38 MAPK inhibitor SB 203580 (1 micromol/L) or buffer (control) for 30 minutes. Cells were then primed with PAF (200 nmol/L), followed by receptor-dependent (N-formyl-methionyl-leucyl-phenylalanine, 1 micromol/L) or receptor-independent phorbol myristate acetate (PMA, 100 ng/mL) activation.

Setting: Urban trauma research laboratory.

Patients: Healthy volunteer donors of neutrophils.

Main outcome measures: Maximal rate of O2- generation was measured by superoxide dismutase-inhibitable reduction of cytochrome c and elastase release by the cleavage of N-methoxysuccinyl-Ala-Ala-Pro-Val-p-nitroanilide.

Results: SB 203580 significantly attenuated the generation of O2- and release of elastase from neutrophils activated with N-formyl-methionyl-leucyl-phenylalanine but not with PMA. Independent of the activator receptor status, SB 203580 almost completely blocked the exaggerated neutrophil cytotoxic response due to PAF priming.

Conclusions: The p38 MAPK pathway is required for maximal PAF-induced neutrophil priming for O2- production and elastase degranulation. Therefore, the MAPK signaling cascade may offer a potential therapeutic strategy to preempt global neutrophil hyperactivity rather than attempt to nullify the end products independently.

Publication types

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

MeSH terms

  • Enzyme Activation
  • Humans
  • Leukocyte Elastase / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neutrophil Activation / physiology*
  • Platelet Activating Factor / pharmacology
  • Superoxides / metabolism*

Substances

  • Platelet Activating Factor
  • Superoxides
  • Mitogen-Activated Protein Kinases
  • Leukocyte Elastase