Regulation of expression of IL-4 alleles:: Analysis using a chimeric GFP/IL-4 gene

被引:122
|
作者
Hu-Li, J
Pannetier, C
Guo, LY
Löhning, M
Gu, H
Watson, C
Assenmacher, M
Radbruch, A
Paul, WE [1 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] Deutsch Rheumaforschungszentrum, D-10117 Berlin, Germany
[3] Miltenyi Biotec, D-51429 Bergisch Gladbach, Germany
关键词
D O I
10.1016/S1074-7613(01)00084-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4 cells from mice heterozygous for an IL-4 and a GFP/IL-4 gene frequently express a single allele. Analysis of IL-4 or GFP production by cells from recently primed Th2 cells indicates that essentially all are competent to transcribe either allele but have a low probability of doing so. By contrast, long-term Th2 clones show distinct and heritable ratios in the proportion of cells that express IL-4 or GFP. We conclude that in the course of Th2 priming an early efficient event renders both alleles capable of being inefficiently transcribed; a second, less frequent event occurs that renders one allele more competent, accounting for the differential expression of IL-4 and GFP in different clones.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 50 条