Chemical inhibitors of TNF signal transduction in human neutrophils point to distinct steps in cell activation

Hyunsil Han, Julia Roberts, Olivia Lou, Willam A. Muller, Noah Nathan, Carl Nathan*

*Corresponding author for this work

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

Chemical screening identified three small compounds that selectively inhibited activation of the respiratory burst (RB) of human neutrophils in response to tumor necrosis factor (TNF) and formylated peptide but not phorbol ester and spared the ability of neutrophils to kill bacteria. These compounds partially inhibited TNF-triggered cytoskeletal rearrangements without blocking adhesion or transmigation of polymorphonuclear neutrophils through TNF-activated monolayers of endothelial cells. The compounds were nontoxic to neutrophils and endothelial cells. They had no direct inhibitory effect on the tyrosine kinases Src, Syk, or Pyk2. However, their differential effects on cell spreading, bacteria-induced RB, TNF-induced degranulation, TNF-induced protein tyrosine phosphorylation, and TNF-induced Syk activation suggested that each may act on different elements of neutrophil signalling pathways.

Original languageEnglish (US)
Pages (from-to)147-154
Number of pages8
JournalJournal of Leukocyte Biology
Volume79
Issue number1
DOIs
StatePublished - Jan 2006

Keywords

  • Phox
  • Respiratory burst
  • Tumor necrosis factor

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Cell Biology

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