rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2002-4-23
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pubmed:abstractText |
Interaction between dendritic cells (DCs) and T cells is a prerequisite for the initiation of a T cell response. The molecular nature of this interaction remains to be fully characterized. We report in this work that freshly isolated mouse splenic DCs and bone marrow-derived DCs express CD137 on the cell surface and in soluble form. Triggering CD137 increased the secretion of IL-6 and IL-12 from DCs. More importantly, infusion of an agonistic mAb to CD137 into naive mice enhanced the ability of DCs to stimulate T cell proliferation in response to both alloantigens and a nominal Ag in vitro. This enhancement of DC function is not mediated through activation of T cells, because the effect was also observed in RAG-1 knockout mice that lack T cells. Our findings implicate CD137 as an important receptor involved in the modulation of DC function.
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pubmed:grant |
|
pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD137,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Nerve Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Tnfrsf9 protein, mouse
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0022-1767
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pubmed:author |
pubmed-author:ChapovalAndrei IAI,
pubmed-author:ChenLiepingL,
pubmed-author:FliesDallas BDB,
pubmed-author:GorskiKevin SKS,
pubmed-author:MittlerRobert SRS,
pubmed-author:OtsujiMizutoM,
pubmed-author:PardollDrew MDM,
pubmed-author:ShinTahiroT,
pubmed-author:TamadaKojiK,
pubmed-author:TsuchiyaHaruoH,
pubmed-author:WilcoxRyan ARA
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
168
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4262-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11970964-Animals,
pubmed-meshheading:11970964-Antibodies, Monoclonal,
pubmed-meshheading:11970964-Antigens, CD,
pubmed-meshheading:11970964-Antigens, CD137,
pubmed-meshheading:11970964-Cells, Cultured,
pubmed-meshheading:11970964-Cytokines,
pubmed-meshheading:11970964-Dendritic Cells,
pubmed-meshheading:11970964-Female,
pubmed-meshheading:11970964-Hematopoietic Stem Cells,
pubmed-meshheading:11970964-Lymphocyte Activation,
pubmed-meshheading:11970964-Mice,
pubmed-meshheading:11970964-Mice, Inbred BALB C,
pubmed-meshheading:11970964-Mice, Inbred C57BL,
pubmed-meshheading:11970964-Receptors, Nerve Growth Factor,
pubmed-meshheading:11970964-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:11970964-Spleen,
pubmed-meshheading:11970964-T-Lymphocytes
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pubmed:year |
2002
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pubmed:articleTitle |
Cutting edge: Expression of functional CD137 receptor by dendritic cells.
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pubmed:affiliation |
Department of Immunology, Mayo Clinic, Rochester, MN 55905, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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