Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1992-6-4
|
pubmed:abstractText |
In bleomycin-induced pulmonary fibrosis, lung injury is accompanied with inflammation and subsequent fibrosis. In this study, lung mRNA for several cytokines was measured in bleomycin-treated mice to evaluate their roles in lung fibrosis. Significant increases in tumor necrosis factor-alpha (TNF-alpha) and transforming growth factor-beta (TGF-beta) mRNA were found in lungs of bleomycin-treated responder CBA mice but not in nonresponder BALB/c mice. Increases in responder animals peaked on day 7 after bleomycin administration, and subsequently returned toward control levels. This time course paralleled that for the increase in beta-actin mRNA, but preceded the peak increase in mRNA for collagens I and III. When lung macrophages were analyzed for cytokine secretion, differences were observed between alveolar macrophages and interstitial cells, and between cells from bleomycin-responsive CBA and nonresponsive BALB/c mice. Only alveolar macrophages from CBA mice secreted increased amounts of IL-1. TNF-alpha activity was increased in conditioned media of alveolar and interstitial cells of CBA mice, while only alveolar macrophages of nonresponder BALB/c mice secreted any activity. The kinetics of the increased secretion of TNF-alpha was dissimilar for these different cells. These results are consistent with the conclusion that increased production of TNF-alpha and TGF-beta is an important component of the fibrotic process.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bleomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0190-2148
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
29-43
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:1374023-Animals,
pubmed-meshheading:1374023-Base Sequence,
pubmed-meshheading:1374023-Bleomycin,
pubmed-meshheading:1374023-Cell Separation,
pubmed-meshheading:1374023-Cytokines,
pubmed-meshheading:1374023-Female,
pubmed-meshheading:1374023-Interleukin-1,
pubmed-meshheading:1374023-Lung,
pubmed-meshheading:1374023-Macrophages, Alveolar,
pubmed-meshheading:1374023-Mice,
pubmed-meshheading:1374023-Mice, Inbred BALB C,
pubmed-meshheading:1374023-Mice, Inbred CBA,
pubmed-meshheading:1374023-Molecular Sequence Data,
pubmed-meshheading:1374023-Pulmonary Fibrosis,
pubmed-meshheading:1374023-RNA, Messenger,
pubmed-meshheading:1374023-Tumor Necrosis Factor-alpha
|
pubmed:articleTitle |
Lung cytokine production in bleomycin-induced pulmonary fibrosis.
|
pubmed:affiliation |
Department of Pathology, University of Michigan Medical School, Ann Arbor 48109-0602.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|