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pubmed-article:11867562pubmed:abstractTextT 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.lld:pubmed
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pubmed-article:11867562pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11867562pubmed:articleTitleReversible CD8 expression induced by common cytokine receptor gamma chain-dependent cytokines in a cloned CD4(+) T(h)1 cell line.lld:pubmed
pubmed-article:11867562pubmed:affiliationDepartment of Oncology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan.lld:pubmed
pubmed-article:11867562pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11867562pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed