Source:http://linkedlifedata.com/resource/pubmed/id/10384129
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1999-7-15
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pubmed:abstractText |
TCR alpha (TCRA) expression was examined in RNA samples from PBMC and isolated populations of CD4+, CD8+, and DN T cells from 15 healthy individuals. The expressed TCR repertoire was surveyed using spectratype analysis, a technique that displays the distribution of complementarity determining region 3 (CDR3) lengths for each TCRAV gene family. The results revealed the presence of unusual populations of double-negative (DN; CD4-CD8-CD3+) T cells that express invariant or conserved TCRAV4A, AV7, AV19, and AV24 chains. Each of the conserved TCRA families was over-represented in >70% of the individuals studied, and all individuals expressed at least one of the over-represented TCRAV families. Over-represented conserved AV4A or AV7 sequences were also present in CD8+ T cells from most donors. The extent of TCRA sequence conservation is unparalleled. TCRAV4A, AV19, and AV24 sequences were invariant, although AV4A and AV19 transcripts contained N region additions. TCRAV24 transcripts derived from the direct juxtaposition of V and J gene segments. TCRAV7 sequences showed some diversity in two amino acids encoded at junctions of V and J gene segments. Although derivation of DN T cells with conserved TCRA chains is puzzling, the wide-spread expression of these unusual cells suggests an important function.
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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, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD4,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD56,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD8,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell...
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
163
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
301-11
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10384129-Adult,
pubmed-meshheading:10384129-Amino Acid Sequence,
pubmed-meshheading:10384129-Antigens, CD3,
pubmed-meshheading:10384129-Antigens, CD4,
pubmed-meshheading:10384129-Antigens, CD56,
pubmed-meshheading:10384129-Antigens, CD8,
pubmed-meshheading:10384129-CD8-Positive T-Lymphocytes,
pubmed-meshheading:10384129-Conserved Sequence,
pubmed-meshheading:10384129-Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor,
pubmed-meshheading:10384129-Humans,
pubmed-meshheading:10384129-Immunophenotyping,
pubmed-meshheading:10384129-Killer Cells, Natural,
pubmed-meshheading:10384129-Molecular Sequence Data,
pubmed-meshheading:10384129-Polymerase Chain Reaction,
pubmed-meshheading:10384129-Receptors, Antigen, T-Cell, alpha-beta,
pubmed-meshheading:10384129-T-Lymphocyte Subsets,
pubmed-meshheading:10384129-Transcription, Genetic
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pubmed:year |
1999
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pubmed:articleTitle |
Invariant or highly conserved TCR alpha are expressed on double-negative (CD3+CD4-CD8-) and CD8+ T cells.
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pubmed:affiliation |
Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, Rockville, MD 20852, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study
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