Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2006-3-20
pubmed:abstractText
Articular adipose tissue is a ubiquitous component of human joints, but its local functions are largely unknown. Because recent studies revealed several links between adipose tissue, adipocytokines, and arthritis, we investigated the expression of the adipocytokine adiponectin and its functional role in articular adipose tissue and synovium of patients with different arthritides. In contrast to its protective role in endocrinological and vascular diseases, adiponectin was found to be involved in key pathways of inflammation and matrix degradation in the human joint. The effects of adiponectin in human synovial fibroblasts appear to be highly selective by inducing only two of the main mediators of rheumatoid arthritis pathophysiology, IL-6 and matrix metalloproteinase-1, via the p38 MAPK pathway. Owing to the observation that these effects could be inhibited by different TNF-alpha inhibitors, adipocytokines such as adiponectin may also be key targets for therapeutic strategies in inflammatory joint diseases. In summary, articular adipose tissue and adipocytokines cannot be regarded as innocent bystanders any more in chronic inflammatory diseases such as arthritis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ADIPOR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Adiponectin, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, Humanized, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6, http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinases, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adiponectin, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha, http://linkedlifedata.com/resource/pubmed/chemical/adalimumab
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
176
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4468-78
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:16547285-Adiponectin, pubmed-meshheading:16547285-Adipose Tissue, pubmed-meshheading:16547285-Antibodies, Monoclonal, pubmed-meshheading:16547285-Antibodies, Monoclonal, Humanized, pubmed-meshheading:16547285-Arthritis, pubmed-meshheading:16547285-Cells, Cultured, pubmed-meshheading:16547285-Fibroblasts, pubmed-meshheading:16547285-Gene Expression Regulation, pubmed-meshheading:16547285-Humans, pubmed-meshheading:16547285-Interleukin-6, pubmed-meshheading:16547285-Matrix Metalloproteinases, pubmed-meshheading:16547285-Protein Binding, pubmed-meshheading:16547285-RNA, Messenger, pubmed-meshheading:16547285-Receptors, Adiponectin, pubmed-meshheading:16547285-Receptors, Cell Surface, pubmed-meshheading:16547285-Signal Transduction, pubmed-meshheading:16547285-Synovial Membrane, pubmed-meshheading:16547285-Tumor Necrosis Factor-alpha
pubmed:year
2006
pubmed:articleTitle
The potential of adiponectin in driving arthritis.
pubmed:affiliation
Department of Internal Medicine I, University Hospital Regensburg, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't