Centromeric repositioning of coreceptor loci predicts their stable silencing and the CD4/CD8 lineage choice

被引:34
作者
Merkenschlager, M
Amoils, S
Roldan, E
Rahemtulla, A
O'Connor, E
Fisher, AG
Brown, KE
机构
[1] Univ London Imperial Coll Sci Technol & Med, MRC, Ctr Clin Sci, Lymphocyte Dev Grp, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, MRC, Flow Cytometry Facil, London W12 0NN, England
[3] Univ London Imperial Coll Sci Technol & Med, MRC, Chromosome Biol Grp, London W12 0NN, England
[4] Hammersmith Hosp, Fac Med, Dept Haematol, London W12 0NN, England
基金
英国医学研究理事会;
关键词
lineage commitment; FISH;
D O I
10.1084/jem.20041127
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The differentiation of CD4(+) CD8(+) double positive (DP) thymocytes requires the irreversible choice between two alternative lineages, distinguished by the mutually exclusive expression of either CD4 or CD8. Differentiating DP cells transiently down-regulate both CD4 and CD8 and this has complicated the debate whether the mechanism of CD4/CD8 lineage choice is instructive, stochastic/selective, or more complex in nature. Using fluorescence in situ hybridization, we show that the stable silencing of coreceptor loci, and ultimately lineage choice, is predicted by the spatial repositioning of coreceptor alleles to centromeric heterochromatin domains. These data provide evidence that lineage-specific developmental programs are established early during the transition from the DP to the single positive stage.
引用
收藏
页码:1437 / 1444
页数:8
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