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Correlation between mRNA expression of Th1/Th2 cytokines and their specific transcription factors in human helper T-cell clones
被引:14
作者:
Kitamura, N
Kaminuma, O
Mori, A
Hashimoto, T
Kitamura, F
Miyagishi, M
Taira, K
Miyatake, S
机构:
[1] Tokyo Metropolitan Inst Med Sci, Dept Immunol, Bunkyo Ku, Tokyo 1138613, Japan
[2] Natl Sagamihara Hosp, Clin Res Ctr Allergy & Rheumatol, Kanagawa, Japan
[3] Univ Tokyo, Sch Engn, Dept Chem & Biotechnol, Tokyo, Japan
关键词:
CD4(+) T cell;
c-Maf;
GATA-3;
T-bet;
Th1/Th2;
cell;
D O I:
10.1111/j.1440-1711.2005.01364.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The mechanisms that underlie Th1/Th2 differentiation of human T cells are incompletely defined. In the present study, a panel of human T-cell clones was used to elucidate the relationship between Th1/Th2-specific transcription factors and cytokine production in human helper T cells. The mRNA expression level of T-bet, a Th1-specific transcription factor, was higher in Th1 clones than in Th2 clones. In contrast, inducible expression of Th2-specific transcription factors (GATA-3 and c-Maf) in Th2 clones was higher than that in Th1 clones. The expression level of T-bet in various T-cell clones was positively correlated with that of IFN-gamma and negatively correlated with that of Th2 cytokines, particularly IL-4. Interestingly, the expression of IL-3 and IL-13, but not of other Th2 cytokines IL-4 and IL-5, was strongly correlated with GATA-3 mRNA levels. A reduction of GATA-3 using RNA interference technology suppressed, whereas overexpression of GATA-3 enhanced, the expression of IL-3 and IL-13. In conclusion, the level of T-bet expression is correlated with Th1/Th2 polarization status, whereas GATA-3 is a crucial factor in determining the IL-3 and IL-13 producing capacity of human T cells.
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页码:536 / 541
页数:6
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