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pubmed-article:15039422pubmed:dateCreated2004-5-24lld:pubmed
pubmed-article:15039422pubmed:abstractTextInterleukin 5 (IL-5) plays a unique role in allergic inflammatory responses, and the understanding of molecular mechanisms underlying the generation of IL-5-producing cells is crucial for the regulation of allergic disorders. Differentiation of naive CD4 T cells into type-2 helper (Th2) cells is accompanied by chromatin remodeling including hyperacetylation of histones H3 and H4 in the nucleosomes associated with the IL-4, IL-13, and IL-5 genes. Histone hyperacetylation of the IL-5 gene displayed a delayed kinetics compared with that of the IL-4 and IL-13 genes, suggesting a distinct remodeling mechanism for the IL-5-gene locus. Here we studied the role of CD28 costimulation in the generation of IL-5-producing cells and the histone hyperacetylation of the IL-5 gene locus. CD28-costimulation selectively enhanced histone hyperacetylation of the IL-5 gene locus that appeared to be mediated through NF-kappaB activation and subsequent up-regulation of GATA3. The CD28 costimulation-sensitive histone hyperacetylation spanned almost the entire intergenic region between the IL-5 and RAD50 accompanied with intergenic transcript. Thus, this is the first demonstration that CD28 costimulation controls a chromatin-remodeling process during Th2 cell differentiation.lld:pubmed
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pubmed-article:15039422pubmed:pagination23123-33lld:pubmed
pubmed-article:15039422pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15039422pubmed:year2004lld:pubmed
pubmed-article:15039422pubmed:articleTitleCD28 costimulation controls histone hyperacetylation of the interleukin 5 gene locus in developing th2 cells.lld:pubmed
pubmed-article:15039422pubmed:affiliationDepartment of Immunology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana Chuo-ku, Chiba 260-8670, Japan.lld:pubmed
pubmed-article:15039422pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15039422pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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