Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6279
|
pubmed:dateCreated |
1990-8-15
|
pubmed:abstractText |
Peptides bound to class I or class II major histocompatibility complex (MHC)-encoded molecules are ligands for the antigen-specific T-cell receptor of T-cells carrying the CD8 and CD4 antigens, respectively. MHC class I-restricted T cells generally recognize peptides derived from processing of endogenously synthesized cellular antigens, whereas class II-restricted T cells usually recognize peptides derived from exogenous antigens entering antigen presenting cells. Accordingly, two separate pathways of antigen processing and presentation have been proposed. The fungal metabolite brefeldin A (BFA), an inhibitor of protein transport from the endoplasmic reticulum, inhibits presentation of endogenous antigens for MHC-restricted T-cell recognition. The selectivity of BFA activity has been inferred to reflect presentation of a given antigen processed through the cytosolic or the endocytic route. Here we show that BFA also greatly inhibits the presentation of exogenous protein antigens by MHC class II molecules to T cells, indicating a broader effect of this drug on antigen presentation and an additional similarity between the two processing pathways. As cycloheximide, a protein synthesis inhibitor, also inhibits presentation of protein antigens to class II-restricted T cells, the data indicate that peptides generated by processing of exogenous proteins binds to newly synthesized class II molecules for presentation to T cells.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Brefeldin A,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclopentanes,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/Muramidase,
http://linkedlifedata.com/resource/pubmed/chemical/Ovalbumin,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0028-0836
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
5
|
pubmed:volume |
346
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
63-6
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2366863-Animals,
pubmed-meshheading:2366863-Antigen-Presenting Cells,
pubmed-meshheading:2366863-Antigens,
pubmed-meshheading:2366863-Brefeldin A,
pubmed-meshheading:2366863-Cell Compartmentation,
pubmed-meshheading:2366863-Cell Line,
pubmed-meshheading:2366863-Cyclopentanes,
pubmed-meshheading:2366863-Histocompatibility Antigens Class II,
pubmed-meshheading:2366863-Mice,
pubmed-meshheading:2366863-Muramidase,
pubmed-meshheading:2366863-Ovalbumin,
pubmed-meshheading:2366863-Peptides,
pubmed-meshheading:2366863-Solubility,
pubmed-meshheading:2366863-T-Lymphocytes
|
pubmed:year |
1990
|
pubmed:articleTitle |
Inhibition by brefeldin A of presentation of exogenous protein antigens to MHC class II-restricted T cells.
|
pubmed:affiliation |
Preclinical Research, Sandoz Pharma Ltd., Basel, Switzerland.
|
pubmed:publicationType |
Journal Article,
In Vitro
|