Source:http://linkedlifedata.com/resource/pubmed/id/15941911
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2005-9-5
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pubmed:abstractText |
Dendritic cells (DCs) and chemokines are important in linking innate and adaptive immunity. We previously reported that Fas ligation induced interleukin 1beta (IL-1beta)-dependent maturation and IL-1beta-independent survival of DCs, with extracellular signal-regulated kinase (ERK) and nuclear factor-kappaB (NF-kappaB) signaling pathways involved, respectively. We describe here that Fas ligation induced DCs to rapidly produce both CXC and CC chemokines, including macrophage inflammatory protein 2 (MIP-2), MIP-1alpha, MIP-1beta, monocyte chemoattractant protein 1 (MCP-1), RANTES (regulated on activation normal T cell expressed and secreted), and TARC (thymus and activation-regulated chemokine), resulting in enhanced chemoattraction of neutrophils and T cells by Fas-ligated DCs in vivo or by its supernatant in vitro. These chemokines work synergistically in chemoattraction of neutrophils and T cells with MIP-2 more important for neutrophils, MIP-1alpha and TARC more important for T cells. Moreover, Fas-ligated DCs increased endocytosis by neutrophils and activation and proliferation of antigen-specific naive T cells. Fas ligation-induced DC secretion of chemokines involves Ras/Raf/mitogen-activated protein kinase kinase (MEK)/ERK activation and is ERK, but not NF-kappaB, dependent. Activation of caspases, including caspase 1, but not IL-1 autocrine action, is involved in this process. These data indicate that Fas signaling provides a key link between innate response and adaptive immunity by promoting DC chemokine production.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD95,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CC,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, CXC,
http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Signal-Regulated MAP...,
http://linkedlifedata.com/resource/pubmed/chemical/Fas protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/ras Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
106
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2033-41
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:15941911-Animals,
pubmed-meshheading:15941911-Antigens, CD95,
pubmed-meshheading:15941911-Caspases,
pubmed-meshheading:15941911-Chemokines, CC,
pubmed-meshheading:15941911-Chemokines, CXC,
pubmed-meshheading:15941911-Chemotaxis,
pubmed-meshheading:15941911-Dendritic Cells,
pubmed-meshheading:15941911-Extracellular Signal-Regulated MAP Kinases,
pubmed-meshheading:15941911-Immunity, Cellular,
pubmed-meshheading:15941911-Immunity, Innate,
pubmed-meshheading:15941911-Mice,
pubmed-meshheading:15941911-Mice, Inbred C57BL,
pubmed-meshheading:15941911-Neutrophils,
pubmed-meshheading:15941911-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:15941911-Signal Transduction,
pubmed-meshheading:15941911-T-Lymphocytes,
pubmed-meshheading:15941911-ras Proteins
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pubmed:year |
2005
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pubmed:articleTitle |
Fas signal links innate and adaptive immunity by promoting dendritic-cell secretion of CC and CXC chemokines.
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pubmed:affiliation |
Institute of Immunology, Second Military Medical University, 800 Xiangyin Rd, Shanghai 200433, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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