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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
15
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pubmed:dateCreated |
1999-1-7
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pubmed:abstractText |
RANTES (regulated upon activation, normal T cell expressed and presumably secreted) and other chemoattractant proteins are members of the intercrine or chemokine family of proinflammatory basic polypeptides. RANTES is a prototype of the C-C chemokine subfamily that acts as a selective chemoattractant for human monocytes and CD4-positive lymphocytes and increases the adherence of monocytes to endothelial cells. However, the role of RANTES in white cells is still unclear. We report here that hrRANTES at 20 ng/50 microl in mice causes mast cell recruitment 4 h after intramuscular injection, an effect inhibited by anti-RANTES, as evidenced by 0.1% Toluidine blue, a specific dye for coloring mast cells. Injections of PBS (50 microl) vehicle (negative control) did not produce any appreciable inflammatory response, whereas injection of lipopolysaccharide 20 ng/50 microl (positive control) generated a marked inflammatory state. When RANTES was injected intramuscularly in genetically mast cell-deficient W/Wv mice, the inflammatory effect was not present. The RANTES injection sites were then excised and studied under an optical and electron microscope. A Northern blot analysis was performed using a probe that was prepared to detect mRNA encoding the histidine decarboxylase (HDC) gene on excised muscle tissue. We found that hrRANTES provoked generation of HDC mRNA from muscle tissue after 4 h. These effects were inhibited by an anti-RANTES antibody and were absent in genetically mast cell-deficient mice. The increasing number of mast cells in the RANTES injection sites led to an augmentation of histamine content compared to controls (PBS). The injection of hrRANTES 20 ng/20 microl into the sole of a rat paw confirmed the inflammatory and the mast cell recruitment potential of this chemokine. In these studies, hrRANTES injections in muscle tissue provided direct in vivo evidence that RANTES has a significant effect on mast cell recruitment and HDC mRNA generation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL5,
http://linkedlifedata.com/resource/pubmed/chemical/Histamine,
http://linkedlifedata.com/resource/pubmed/chemical/Histidine Decarboxylase,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Tolonium Chloride
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0892-6638
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1693-700
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9837859-Animals,
pubmed-meshheading:9837859-Chemokine CCL5,
pubmed-meshheading:9837859-Extremities,
pubmed-meshheading:9837859-Histamine,
pubmed-meshheading:9837859-Histidine Decarboxylase,
pubmed-meshheading:9837859-Humans,
pubmed-meshheading:9837859-Injections, Intramuscular,
pubmed-meshheading:9837859-Injections, Subcutaneous,
pubmed-meshheading:9837859-Mast Cells,
pubmed-meshheading:9837859-Mice,
pubmed-meshheading:9837859-Mice, Mutant Strains,
pubmed-meshheading:9837859-Muscle, Skeletal,
pubmed-meshheading:9837859-RNA, Messenger,
pubmed-meshheading:9837859-Rats,
pubmed-meshheading:9837859-Recombinant Proteins,
pubmed-meshheading:9837859-Staining and Labeling,
pubmed-meshheading:9837859-Tolonium Chloride
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pubmed:year |
1998
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pubmed:articleTitle |
Intramuscular injection of hrRANTES causes mast cell recruitment and increased transcription of histidine decarboxylase in mice: lack of effects in genetically mast cell-deficient W/WV mice.
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pubmed:affiliation |
Immunology Division, University of Chieti School of Medicine, Chieti, Italy. pconti@unich.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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