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Helper T cell differentiation is controlled by the cell cycle
被引:745
作者:
Bird, JJ
Brown, DR
Mullen, AC
Moskowitz, NH
Mahowald, MA
Sider, JR
Gajewski, TF
Wang, CR
Reiner, SL
[1
]
机构:
[1] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[3] Univ Chicago, Gwen Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
[4] Univ Chicago, Comm Dev Biol, Chicago, IL 60637 USA
[5] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
来源:
关键词:
D O I:
10.1016/S1074-7613(00)80605-6
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Helper T (Th) cell differentiation is highly regulated by cytokines but initiated by mitogens. By examining gene expression in discrete generations of dividing cells, we have delineated the relationship between proliferation and differentiation. Initial expression of IL-2 is cell cycle-independent, whereas effector cytokine expression is cell cycle-dependent. IFN gamma expression increases in frequency with successive cell cycles, while IL-4 expression requires three cell divisions. Cell cycle progression and cytokine signaling act in concert Po relieve epigenetic repression and can be supplanted by agents that hyperacetylate histones and demethylate DNA. Terminally differentiated cells exhibit stable epigenetic modification and cell cycle-independent gene expression. These data reveal a novel mechanism governing Th cell fate that initially integrates proliferative and differentiative signals and subsequently maintains stability of the differentiated state.
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页码:229 / 237
页数:9
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