Modulation of endotoxin-induced endothelial activity by microtubule depolymerization

J Trauma. 2003 Jan;54(1):104-12; discussion 112-3. doi: 10.1097/00005373-200301000-00013.

Abstract

Background: Endotoxin not only activates the Toll-mediated signaling pathway within endothelial cells that leads to neutrophil migration but also causes the polymerization of microtubules. The potential role of this polymerization event, however, is unknown.

Methods: Human umbilical vein endothelial cells stimulated with endotoxin were pretreated with or without the microtubule depolymerizing agent colchicine. Toll-mediated signaling events and protein production were in turn investigated by Western blot, gel shift, and enzyme-linked immunosorbent assay. Finally, neutrophil adhesion was assayed fluorometrically under the various conditions.

Results: Endotoxin led to activation of the various Toll-mediated pathways, production of intercellular adhesion molecule-1 and interleukin-8, and subsequent neutrophil adhesion. Pretreatment with colchicine led to selective inhibition of anti-dual phosphorylated extracellular signal-regulated kinase-1/2, anti-dual phosphorylated c-jun N-terminal kinase, and adaptor protein-1; selective enhancement of p38; and no effect on nuclear factor-kappaB. This selective modulation of intracellular signaling resulted in attenuated intercellular adhesion molecule-1, interleukin-8 and prostaglandin E2 production, but enhanced cyclooxygenase-2 expression. As a result, microtubule disruption led to a significant reduction in neutrophil adhesion.

Conclusion: Microtubule formation is essential to optimal endotoxin-induced intracellular signaling through anti-dual phosphorylated extracellular signal-regulated kinase-1/2, anti-dual phosphorylated c-jun N-terminal kinase, and adaptor protein-1. Failure of these signaling events is associated with a marked reduction in the formation of a proadhesive phenotype that may prove to be beneficial in modulating neutrophil recruitment during sepsis.

Publication types

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

MeSH terms

  • Adaptor Protein Complex 1 / immunology
  • Blotting, Western
  • Cells, Cultured
  • Colchicine / pharmacology
  • Cyclooxygenase 2
  • Dinoprostone / immunology
  • Drosophila Proteins*
  • Electrophoretic Mobility Shift Assay
  • Endothelium, Vascular / cytology*
  • Endothelium, Vascular / immunology*
  • Enzyme-Linked Immunosorbent Assay
  • Escherichia coli*
  • Humans
  • Intercellular Adhesion Molecule-1 / immunology
  • Interleukin-8 / immunology
  • Isoenzymes / immunology
  • JNK Mitogen-Activated Protein Kinases
  • Lipopolysaccharides / adverse effects*
  • Membrane Glycoproteins / immunology
  • Membrane Proteins
  • Microtubules / immunology*
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases / immunology
  • NF-kappa B / immunology
  • Neutrophil Activation / immunology
  • Neutrophil Infiltration / immunology
  • Polymers
  • Prostaglandin-Endoperoxide Synthases / immunology
  • Receptors, Cell Surface / immunology
  • Sepsis / immunology*
  • Signal Transduction / immunology
  • Toll-Like Receptors
  • Umbilical Veins / cytology

Substances

  • Adaptor Protein Complex 1
  • Drosophila Proteins
  • Interleukin-8
  • Isoenzymes
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • Membrane Proteins
  • NF-kappa B
  • Polymers
  • Receptors, Cell Surface
  • Toll-Like Receptors
  • Intercellular Adhesion Molecule-1
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases
  • Dinoprostone
  • Colchicine