Source:http://linkedlifedata.com/resource/pubmed/id/15284116
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2004-11-4
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pubmed:abstractText |
Exosomes are nanovesicles released by leukocytes and epithelial cells. Although their function remains enigmatic, exosomes are a source of antigen and transfer functional major histocompatibility complex (MHC)-I/peptide complexes to dendritic cells (DCs) for CD8(+) T-cell activation. Here we demonstrate that exosomes also are internalized and processed by immature DCs for presentation to CD4(+) T cells. Endocytosed exosomes are sorted into the endocytic compartment of DCs for processing, followed by loading of exosome-derived peptides in MHC-II molecules for presentation to CD4(+) T cells. Targeting of exosomes to DCs is mediated via milk fat globule (MFG)-E8/lactadherin, CD11a, CD54, phosphatidylserine, and the tetraspanins CD9 and CD81 on the exosome and alpha(v)/beta(3) integrin, and CD11a and CD54 on the DCs. Circulating exosomes are internalized by DCs and specialized phagocytes of the spleen and by hepatic Kupffer cells. Internalization of blood-borne allogeneic exosomes by splenic DCs does not affect DC maturation and is followed by loading of the exosome-derived allopeptide IEalpha(52-68) in IA(b) by host CD8alpha(+) DCs for presentation to CD4(+) T cells. These data imply that exosomes present in circulation or extracellular fluids constitute an alternative source of self- or allopeptides for DCs during maintenance of peripheral tolerance or initiation of the indirect pathway of allorecognition in transplantation.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/P01 CA73743,
http://linkedlifedata.com/resource/pubmed/grant/R01 075512,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI41011,
http://linkedlifedata.com/resource/pubmed/grant/R01 AI43916,
http://linkedlifedata.com/resource/pubmed/grant/R01 CA100893,
http://linkedlifedata.com/resource/pubmed/grant/R01 DK49745,
http://linkedlifedata.com/resource/pubmed/grant/R21 AI55027,
http://linkedlifedata.com/resource/pubmed/grant/R21 AI57958,
http://linkedlifedata.com/resource/pubmed/grant/R21 HL69725
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:FaloLouis DLDJr,
pubmed-author:LarreginaAdriana TAT,
pubmed-author:LogarAlison JAJ,
pubmed-author:MorelliAdrian EAE,
pubmed-author:PapworthGlenn DGD,
pubmed-author:ShufeskyWilliam JWJ,
pubmed-author:StolzDonna BeerDB,
pubmed-author:SullivanMara L GML,
pubmed-author:ThomsonAngus WAW,
pubmed-author:WangZhiliangZ,
pubmed-author:WatkinsSimon CSC,
pubmed-author:ZahorchakAlan FAF
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3257-66
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15284116-Animals,
pubmed-meshheading:15284116-Antigen Presentation,
pubmed-meshheading:15284116-Antigens, Surface,
pubmed-meshheading:15284116-CD4-Positive T-Lymphocytes,
pubmed-meshheading:15284116-Dendritic Cells,
pubmed-meshheading:15284116-Endocytosis,
pubmed-meshheading:15284116-Immune Tolerance,
pubmed-meshheading:15284116-Injections, Intravenous,
pubmed-meshheading:15284116-Isoantigens,
pubmed-meshheading:15284116-Mice,
pubmed-meshheading:15284116-Mice, Inbred BALB C,
pubmed-meshheading:15284116-Mice, Inbred C57BL,
pubmed-meshheading:15284116-Phagocytosis,
pubmed-meshheading:15284116-Protein Transport,
pubmed-meshheading:15284116-Spleen
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pubmed:year |
2004
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pubmed:articleTitle |
Endocytosis, intracellular sorting, and processing of exosomes by dendritic cells.
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pubmed:affiliation |
Thomas E. Starzl Transplantation Institute, Department of Surgery, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA. morelli@imap.pitt.edu.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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