rdf:type |
|
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0017262,
umls-concept:C0079189,
umls-concept:C0085358,
umls-concept:C0185117,
umls-concept:C0205214,
umls-concept:C0205263,
umls-concept:C0206552,
umls-concept:C1332714,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1522642,
umls-concept:C1552644,
umls-concept:C1706438,
umls-concept:C1823153,
umls-concept:C2349976,
umls-concept:C2698600,
umls-concept:C2911684
|
pubmed:issue |
3
|
pubmed:dateCreated |
2002-2-27
|
pubmed:abstractText |
T cells that are intrathymically lineage committed are believed to maintain their CD4 or CD8 co-receptor expression. Here, we investigated whether intrathymic lineage commitment involves irreversible genetic modification or whether co-receptor expression can be reprogrammed depending on external stimuli. The CD4(+) T(h)1 clone 2D6 established from splenic T cells as an IL-12-dependent line survived in culture with IL-2, IL-7 or IL-15 alone. Surprisingly, CD8 expression occurred in 2D6 cells upon replacement of IL-12 with any one of the three cytokines that stimulate the common cytokine receptor gamma chain, yielding CD4(+)CD8(+) 2D6 cells. CD8 expression declined when IL-2 was replaced with IL-12 and CD8 induction was inhibited when IL-12 was included in IL-2 or IL-7 culture. Our observations show that even a lineage-committed mature T cell can be reprogrammed for co-receptor expression in response to particular external stimuli.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD8,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Il2rg protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin Receptor Common gamma...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-15,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-7,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-7
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0953-8178
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
259-66
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11867562-Animals,
pubmed-meshheading:11867562-Antigens, CD8,
pubmed-meshheading:11867562-Clone Cells,
pubmed-meshheading:11867562-Cytokines,
pubmed-meshheading:11867562-Gene Expression Regulation,
pubmed-meshheading:11867562-Interleukin Receptor Common gamma Subunit,
pubmed-meshheading:11867562-Interleukin-12,
pubmed-meshheading:11867562-Interleukin-15,
pubmed-meshheading:11867562-Interleukin-2,
pubmed-meshheading:11867562-Interleukin-4,
pubmed-meshheading:11867562-Interleukin-7,
pubmed-meshheading:11867562-Mice,
pubmed-meshheading:11867562-Mice, Inbred C57BL,
pubmed-meshheading:11867562-Receptors, Interleukin-7,
pubmed-meshheading:11867562-Th1 Cells
|
pubmed:year |
2002
|
pubmed:articleTitle |
Reversible CD8 expression induced by common cytokine receptor gamma chain-dependent cytokines in a cloned CD4(+) T(h)1 cell line.
|
pubmed:affiliation |
Department of Oncology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|