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A Critical Role for LTA 4 H in Limiting Chronic Pulmonary Neutrophilic Inflammation
Author(s) -
Robert J. Snelgrove,
Patricia L. Jackson,
Matthew T. Hardison,
Brett D. Noerager,
A. J. Kinloch,
Amit Gaggar,
Suresh Shastry,
Steven M. Rowe,
Yun M. Shim,
Tracy Hussell,
J. Edwin Blalock
Publication year - 2010
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1190594
Subject(s) - leukotriene b4 , copd , inflammation , proinflammatory cytokine , aminopeptidase , chemokine , immunology , chemistry , biology , medicine , biochemistry , amino acid , leucine
Leukotriene A(4) hydrolase (LTA(4)H) is a proinflammatory enzyme that generates the inflammatory mediator leukotriene B(4) (LTB(4)). LTA(4)H also possesses aminopeptidase activity with unknown substrate and physiological importance; we identified the neutrophil chemoattractant proline-glycine-proline (PGP) as this physiological substrate. PGP is a biomarker for chronic obstructive pulmonary disease (COPD) and is implicated in neutrophil persistence in the lung. In acute neutrophil-driven inflammation, PGP was degraded by LTA(4)H, which facilitated the resolution of inflammation. In contrast, cigarette smoke, a major risk factor for the development of COPD, selectively inhibited LTA(4)H aminopeptidase activity, which led to the accumulation of PGP and neutrophils. These studies imply that therapeutic strategies inhibiting LTA(4)H to prevent LTB(4) generation may not reduce neutrophil recruitment because of elevated levels of PGP.

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