TITLE

Critical role for CXCR2 and CXCR2 ligands during the pathogenesis of ventilator-induced lung injury

AUTHOR(S)
Belperio, John A.; Keane, Michael P.; Burdick, Marie D.; Londhe, Vedang; Ying Ying Xue; Kewang Li; Phillips, Roderick J.; Strieter, Robert M.; Xue, Ying Ying; Li, Kewang
PUB. DATE
December 2002
SOURCE
Journal of Clinical Investigation;12/1/2002, Vol. 110 Issue 11, p1703
SOURCE TYPE
Academic Journal
DOC. TYPE
journal article
ABSTRACT
Mortality related to adult respiratory distress syndrome (ARDS) ranges from 35% to 65%. Lung-protective ventilator strategies can reduce mortality during ARDS. The protective strategies limit tidal volumes and peak pressures while maximizing positive end-expiratory pressure. The efficacy of this approach is due to a reduction of shear-stress of the lung and release of inflammatory mediators. Ventilator-induced lung injury (VILI) is characterized by inflammation. The specific mechanism(s) that recruit leukocytes during VILI have not been elucidated. Because the murine CXC chemokines KC/CXCL1 and MIP-2/CXCL2/3, via CXCR2, are potent neutrophil chemoattractants, we investigated their role in a murine model of VILI. We compared two ventilator strategies in C57BL/6 mice: high peak pressure and high stretch (high peak pressure/stretch) versus low peak pressure/stretch for 6 hours. Lung injury and neutrophil sequestration from the high-peak pressure/stretch group were greater than those from the low-peak pressure/stretch group. In addition, lung expression of KC/CXCL1 and MIP-2/CXCL2/3 paralleled lung injury and neutrophil sequestration. Moreover, in vivo inhibition of CXCR2/CXC chemokine ligand interactions led to a marked reduction in neutrophil sequestration and lung injury. These findings were confirmed using CXCR2(-/-) mice. Together these experiments support the notion that increased expression of KC/CXCL1 and MIP-2/CXCL2/3 and their interaction with CXCR2 are important in the pathogeneses of VILI.
ACCESSION #
9062096

 

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