Kinetic analysis of genomewide gene expression reveals molecule circuitries that control T cell activation and Th1/2 differentiation

被引:44
作者
Lu, BF
Zagouras, P
Fischer, JE
Lu, JF
Li, BY
Flavell, RA
机构
[1] Yale Univ, Sch Med, Immunobiol Sect, Howard Hughes Med Inst, New Haven, CT 06520 USA
[2] Pfizer Inc, Pfizer Global Res & Dev, Groton Labs, Groton, CT 06340 USA
[3] Univ Kentucky, Ctr Biomed Engn, Lexington, KY 40506 USA
关键词
D O I
10.1073/pnas.0307743100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The global gene expression profiling of early T helper (Th) 1 and Th2 differentiation reveals that this process can be divided into two stages, activation and differentiation. The activation stage is manifested in coordinated mobilization of the replication machinery, a process that we hypothesize may be responsible for establishing genomewide opening of transcription loci. The molecular programs underlying the differentiation stage consist of highly regulated expression of functional groups of genes that are important for the biological properties of Th1/2 cells and transcription factors that are likely important in establishing terminal differentiation of these cells. The kinetics of expression pattern of a number of transcription factors shed new light on the molecular events that shape the outcome of Th1/2 differentiation.
引用
收藏
页码:3023 / 3028
页数:6
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