Source:http://linkedlifedata.com/resource/pubmed/id/15020295
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2004-9-9
|
pubmed:abstractText |
Myeloperoxidase (MPO)-derived oxidants participate in the respiratory antimicrobial defense system but are also implicated in oxidant-mediated acute lung injury. We hypothesized that MPO contributes to lung injury commonly observed after bone marrow transplantation (BMT). MPO-sufficient (MPO+/+) and -deficient (MPO-/-) mice were given cyclophosphamide and lethally irradiated followed by infusion of inflammation-inducing donor spleen T cells at time of BMT. Despite suppressed generation of nitrative stress, MPO-/- recipient mice unexpectedly exhibited accelerated weight loss and increased markers of lung dysfunction compared with MPO+/+ mice. The increased lung injury during MPO deficiency was a result of donor T cell-dependent inflammatory responses because bronchoalveolar lavage fluids (BALF) from MPO-/- mice contained increased numbers of inflammatory cells and higher levels of the proinflammatory cytokine TNF-alpha and the monocyte chemoattractant protein-1 compared with wild-type mice. Enhanced inflammation in MPO-/- mice was associated with suppressed apoptosis of BALF inflammatory cells. The inflammatory process in MPO-/- recipients was also associated with enhanced necrosis of freshly isolated alveolar type II cells, critical for preventing capillary leak. We conclude that suppressed MPO-derived oxidative/nitrative stress is associated with enhanced lung inflammation and persistent alveolar epithelial injury.
|
pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1040-0605
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
287
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
L706-14
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:15020295-Animals,
pubmed-meshheading:15020295-Bone Marrow Transplantation,
pubmed-meshheading:15020295-Bronchoalveolar Lavage Fluid,
pubmed-meshheading:15020295-Inflammation,
pubmed-meshheading:15020295-Lung Injury,
pubmed-meshheading:15020295-Mice,
pubmed-meshheading:15020295-Mice, Inbred C57BL,
pubmed-meshheading:15020295-Mice, Inbred Strains,
pubmed-meshheading:15020295-Mice, Knockout,
pubmed-meshheading:15020295-Oxidative Stress,
pubmed-meshheading:15020295-Peroxidase,
pubmed-meshheading:15020295-Pulmonary Alveoli,
pubmed-meshheading:15020295-T-Lymphocytes,
pubmed-meshheading:15020295-Transplantation, Homologous
|
pubmed:year |
2004
|
pubmed:articleTitle |
Myeloperoxidase deficiency enhances inflammation after allogeneic marrow transplantation.
|
pubmed:affiliation |
Division of Pulmonary and Critical Care, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota 55455, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|