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Intracellular Mechanisms of Hydrogen Peroxide-Mediated Neutrophil Adherence to Cultured Human Endothelial Cells

Authors
Journal
Microvascular Research
0026-2862
Publisher
Elsevier
Publication Date
Volume
57
Issue
2
Identifiers
DOI: 10.1006/mvre.1998.2117
Keywords
  • Protein Kinase C
  • Intracellular Calcium
  • Protein Kinase G
  • Protein Kinase A
  • Tyrosine Kinase
Disciplines
  • Biology

Abstract

Abstract We examined which endothelial second messengers are involved in peroxide-mediated endothelial–neutrophil adhesion with respect to endothelial P-selectin expression and platelet-activating factor (PAF). Peroxide (0.5 mM)-mediated adhesion was blocked by a protein kinase C (PKC) inhibitor, Gö6976 (10 nM); an intracellular calcium chelator, TMB-8 (0.1 mM); and a protein kinase G (PKG) inhibitor, KT5823 (0.5 μM); but not by a tyrosine kinase inhibitor, genistein (1 μM), or a protein kinase A inhibitor, H-89 (0.1 μM). These data were consistent with the proadhesive effects of PMA (0.1 μM), a PKC activator; a calcium ionophore, A23187 (1 μM); and dibutyryl cGMP (0.5 and 1 mM); but not phenylarsine oxide (0.1 mM), a tyrosine phosphatase inhibitor, or dibutyryl cAMP (1 mM). Conversely, peroxide-mediated P-selectin expression was blocked by Gö6976 and KT5823, but not by TMB-8. These data are strengthened by the observation that PMA and dibutyryl cGMP, but not A23187, increased P-selectin expression. WEB 2086 (10 μM), a PAF-receptor antagonist, blocked peroxide-, PMA-, and A23187-mediated adhesion, but not peroxide-mediated P-selectin expression. PAF itself (10 nM) stimulated adhesion, but not P-selectin expression. These data indicate that PKC and PKG are involved in peroxide-mediated neutrophil adhesion via P-selectin mobilization and PAF synthesis; however, intracellular calcium appears to mediate adhesion only through PAF synthesis.

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