Medical Journals

Complete Reversal of Acid-induced Acute Lung Injury by Blocking of Platelet-neutrophil Aggregation.

Authors:
  • Zarbock Alexander
  • Singbartl Kai
  • Ley Klaus

From: Robert M Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22908-1394, USA.

The Journal of clinical investigation

  • Publish Date: Dec 2006
  • ISSN: 0021-9738
  • Volume: 116
  • Issue: 12
  • Pages: 3211-9
  • Medium: Print
  • Language: English
  • Citation (JAMA): Zarbock Alexander, Singbartl Kai, Ley Klaus, et al. Complete Reversal of Acid-induced Acute Lung Injury by Blocking of Platelet-neutrophil Aggregation.. J. Clin. Invest. Dec 2006;116:3211-9

Abstract

Acute lung injury (ALI) causes high mortality, but its molecular mechanisms are poorly understood. Acid aspiration is a frequent cause of ALI, leading to neutrophil sequestration, increased permeability, and deterioration of gas exchange. We investigated the role of platelet-neutrophil interactions in a murine model of acid-induced ALI. Acid aspiration induced P-selectin-dependent platelet-neutrophil interactions in blood and in lung capillaries. Reducing circulating platelets or blocking P-selectin halted the development of ALI. Bone marrow chimeras showed that platelet, not endothelial, P-selectin was responsible for the injury. The interaction of platelets with neutrophils and endothelia was associated with TXA(2) formation, with detrimental effects on permeability and tissue function. Activated platelets induced endothelial expression of ICAM-1 and increased neutrophil adhesion. Inhibition of platelet-neutrophil aggregation improved gas exchange, reduced neutrophil recruitment and permeability, and prolonged survival. The key findings were confirmed in a sepsis-induced model of ALI. These findings may translate into improved clinical treatments for ALI.

Mesh Headings (Keywords): Acids, Animals, Blood Platelets, Busulfan, Cell Adhesion, Cell Communication, Cells, Cultured, Disease Models, Animal, Endothelial Cells, Flow Cytometry, Humans, Lung, Mice, Mice, Inbred C57BL, Neutrophil Activation, Neutrophils, P-Selectin, Platelet Activation, Platelet Aggregation, Receptors, Thromboxane, Respiratory Distress Syndrome, Adult


Check for Full Text / PubMed Unique Identifier (PMID): 17143330


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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