Independent and epigenetic regulation of the interleukin-4 alleles in CD4+ T cells

被引:208
|
作者
Bix, M
Locksley, RM
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Immunol Microbiol, San Francisco, CA 94143 USA
关键词
D O I
10.1126/science.281.5381.1352
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
How an individual effector T cell acquires a particular cytokine expression pattern from many possible patterns remains unclear. CD4(+) T cells from F-1 mice, which allowed assignment of the parental origin of interleukin-4 (IL-4) transcripts, were divided into clones that expressed IL-4 biallelically or monoallelically from either allele. The allelic pattern was transmitted as a stable epigenetic trait. Regulation of cytokine expression by a mechanism that treats each allele independently suggests a probabilistic process by which a diverse repertoire of combinatorially assorted cytokine gene expression patterns could be generated among the clonally related daughters of a single precursor cell.
引用
收藏
页码:1352 / 1354
页数:3
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