|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0016059,
umls-concept:C0032285,
umls-concept:C0040690,
umls-concept:C0205275,
umls-concept:C0253930,
umls-concept:C0330390,
umls-concept:C0441712,
umls-concept:C1145667,
umls-concept:C1515877,
umls-concept:C1879547,
umls-concept:C1998811
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
1999-3-3
|
|
pubmed:abstractText |
Transforming growth factor beta (TGF beta) family members are secreted in inactive complexes with a latency-associated peptide (LAP), a protein derived from the N-terminal region of the TGF beta gene product. Extracellular activation of these complexes is a critical but incompletely understood step in regulation of TGF beta function in vivo. We show that TGF beta 1 LAP is a ligand for the integrin alpha v beta 6 and that alpha v beta 6-expressing cells induce spatially restricted activation of TGF beta 1. This finding explains why mice lacking this integrin develop exaggerated inflammation and, as we show, are protected from pulmonary fibrosis. These data identify a novel mechanism for locally regulating TGF beta 1 function in vivo by regulating expression of the alpha v beta 6 integrin.
|
|
pubmed:grant |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/Bleomycin,
http://linkedlifedata.com/resource/pubmed/chemical/Integrins,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta1,
http://linkedlifedata.com/resource/pubmed/chemical/integrin alphavbeta6
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Feb
|
|
pubmed:issn |
0092-8674
|
|
pubmed:author |
pubmed-author:DaltonS LSL,
pubmed-author:GarbeSS,
pubmed-author:GriffithsM JMJ,
pubmed-author:HuangXX,
pubmed-author:KaminskiNN,
pubmed-author:KawakatsuHH,
pubmed-author:MatthayM AMA,
pubmed-author:MungerJ SJS,
pubmed-author:PittetJ FJF,
pubmed-author:RifkinD BDB,
pubmed-author:SheppardDD,
pubmed-author:WuJJ
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
5
|
|
pubmed:volume |
96
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
319-28
|
|
pubmed:dateRevised |
2007-11-14
|
|
pubmed:meshHeading |
pubmed-meshheading:10025398-3T3 Cells,
pubmed-meshheading:10025398-Animals,
pubmed-meshheading:10025398-Antigens, Neoplasm,
pubmed-meshheading:10025398-Bleomycin,
pubmed-meshheading:10025398-CHO Cells,
pubmed-meshheading:10025398-Cricetinae,
pubmed-meshheading:10025398-Epithelial Cells,
pubmed-meshheading:10025398-Esophagus,
pubmed-meshheading:10025398-Humans,
pubmed-meshheading:10025398-Integrins,
pubmed-meshheading:10025398-Keratinocytes,
pubmed-meshheading:10025398-Ligands,
pubmed-meshheading:10025398-Mice,
pubmed-meshheading:10025398-Mice, Knockout,
pubmed-meshheading:10025398-Peptide Fragments,
pubmed-meshheading:10025398-Protein Binding,
pubmed-meshheading:10025398-Protein Precursors,
pubmed-meshheading:10025398-Proteins,
pubmed-meshheading:10025398-Pulmonary Fibrosis,
pubmed-meshheading:10025398-Transforming Growth Factor beta,
pubmed-meshheading:10025398-Transforming Growth Factor beta1,
pubmed-meshheading:10025398-Tumor Cells, Cultured
|
|
pubmed:year |
1999
|
|
pubmed:articleTitle |
The integrin alpha v beta 6 binds and activates latent TGF beta 1: a mechanism for regulating pulmonary inflammation and fibrosis.
|
|
pubmed:affiliation |
Department of Medicine, and Kaplan Cancer Center, New York University School of Medicine, New York 10016-6402, USA.
|
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|
