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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1996-6-13
|
| pubmed:abstractText |
In the present study, we investigated the developmental potential of purified populations of transitional CD4inCD8hi and CD4hiCD8in thymocytes that were further defined according to their differentiation stage by their levels of T cell receptor (TCR) expression into TCRlo, TCRin and TCRhi subpopulations. The differentiation potential of each of these subsets was tested in vitro in a single-cell suspension culture assay that showed that CD4inCD8hiTCRhi are precursors of CD8 single-positive cells, whereas CD4hiCD8inTCRin/hi are precursors of both CD4 and CD8 single-positive thymocytes. The analysis of transitional subsets in mutant mice for either beta 2-microglobulin or major histocompatibility complex (MHC) class II further revealed that lineage commitment to the CD8 lineage requires a TCR-MHC class I engagement, presumably at the immature double-positive stage of thymic development, while CD4 commitment does not require an MHC class II-mediated signal, but rather occurs by default. Using the addition of MHC class I- or class II-expressing cells or the addition of total thymocytes to purified sorted transitional precursors for the duration of the cultures in vitro, we identified an additional stage of differentiation for both CD4 and CD8 lineages that requires a positive selection signal. Examination of protein tyrosine phosphorylation of transitional precursors revealed that CD4inCD8hi transitional cells contain a high level of a 70-kDa phosphorylated protein consistent with a role for ZAP70 in the signal transduction during the positive selection of CD8+ cells.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0014-2980
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
26
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
461-71
|
| pubmed:dateRevised |
2009-11-19
|
| pubmed:meshHeading |
pubmed-meshheading:8617319-Animals,
pubmed-meshheading:8617319-CD4-Positive T-Lymphocytes,
pubmed-meshheading:8617319-CD8-Positive T-Lymphocytes,
pubmed-meshheading:8617319-Cell Differentiation,
pubmed-meshheading:8617319-Cell Separation,
pubmed-meshheading:8617319-Cells, Cultured,
pubmed-meshheading:8617319-Histocompatibility Antigens Class I,
pubmed-meshheading:8617319-Histocompatibility Antigens Class II,
pubmed-meshheading:8617319-Immunophenotyping,
pubmed-meshheading:8617319-Lymphocyte Activation,
pubmed-meshheading:8617319-Mice,
pubmed-meshheading:8617319-Mice, Inbred C57BL,
pubmed-meshheading:8617319-Mice, Knockout,
pubmed-meshheading:8617319-Phosphorylation,
pubmed-meshheading:8617319-Protein-Tyrosine Kinases,
pubmed-meshheading:8617319-Signal Transduction,
pubmed-meshheading:8617319-Stromal Cells,
pubmed-meshheading:8617319-Thymus Gland
|
| pubmed:year |
1996
|
| pubmed:articleTitle |
CD8/CD4 lineage commitment occurs by an instructional/default process followed by positive selection.
|
| pubmed:affiliation |
Division of Immunology and Cancer Research, The Hospital for Sick Children, Toronto, Canada.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|