How are TH1 and TH2 effector cells made?

被引:127
作者
Amsen, Derk [2 ]
Spilianakis, Charalampos G. [3 ]
Flavell, Richard A. [1 ,4 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] Univ Amsterdam, Acad Med Ctr, Dept Cell Biol & Histol, NL-1105 AZ Amsterdam, Netherlands
[3] Fdn Res & Technol, Inst Mol Biol & Biotechnol, GR-71110 Vassilika Vouton, Crete, Greece
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
DISTAL REGULATORY ELEMENTS; TYPE-1 CYTOKINE RESPONSES; ENCODING INTERFERON-GAMMA; LOCUS-CONTROL REGION; CD4; T-CELLS; NF-KAPPA-B; DENDRITIC CELLS; IN-VIVO; GATA3; EXPRESSION; GENE-EXPRESSION;
D O I
10.1016/j.coi.2009.03.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Differentiation of T(H)1 and T(H)2 effector cells proceeds through several phases: First, naive CD4(+) precursor cells are instructed to differentiate as appropriate to optimally fight the infectious threat encountered. This process is governed by the IL12 and IL4 cytokines, as well as by signaling through the Notch receptor. In response to these signals, transcription is initiated of lineage specific cytokine genes including the Ifn gamma and 114 genes as well as of genes encoding transcriptional regulators, such as T-bet and Gata3. The respective differentiation programs are reinforced by both positive and negative feedback mechanisms. Furthermore, epigenetic modifications of the lineage specific genes result in the emergence of regulatory elements, which control high level lineage restricted expression by both intrachromosomal and interchromosomal associations. Together, these mechanisms ensure stable inheritance of the differentiated fate in the numerous progeny of the original naive CD4(+) T cells.
引用
收藏
页码:153 / 160
页数:8
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