首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Critical role of transcription factor PU.1 in the expression of CD80 and CD86 on dendritic cells.
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Critical role of transcription factor PU.1 in the expression of CD80 and CD86 on dendritic cells.

机译:转录因子PU.1在树突状细胞中CD80和CD86表达中的关键作用。

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摘要

In this study, we investigated the role of a transcription factor, PU.1, in the regulation of CD80 and CD86 expression in dendritic cells (DCs). A chromatin immunoprecipitation assay revealed that PU.1 is constitutively bound to the CD80 and CD86 promoters in bone marrow-derived DCs. In addition, co-expression of PU.1 resulted in the transactivation of the CD80 and CD86 promoters in a reporter assay. The binding of PU.1 to cis-enhancing regions was confirmed by electromobility gel-shift assay. As expected, inhibition of PU.1 expression by short interfering RNA (siRNA) in bone marrow-derived DCs resulted in marked down-regulation of CD80 and CD86 expression. Moreover, overexpression of PU.1 in murine bone marrow-derived lineage-negative cells induced the expression of CD80 and CD86 in the absence of monocyte/DC-related growth factors and/or cytokines. Based on these results, we conclude that PU.1 is a critical factor for the expression of CD80 and CD86. We also found that subcutaneous injection of PU.1 siRNA or topical application of a cream-emulsified PU.1 siRNA efficiently inhibited murine contact hypersensitivity. Our results suggest that PU.1 is a potential target for the treatment of immune-related diseases.
机译:在这项研究中,我们调查了转录因子PU.1在树突状细胞(DC)中CD80和CD86表达调控中的作用。染色质免疫沉淀试验表明,PU.1与骨髓来源的DC中的CD80和CD86启动子组成性结合。此外,PU.1的共表达导致在报告基因分析中CD80和CD86启动子的反式激活。 PU.1与顺式增强区的结合通过电动迁移凝胶位移测定法得以证实。不出所料,骨髓来源的DC中短干扰RNA(siRNA)对PU.1表达的抑制导致CD80和CD86表达的明显下调。此外,在不存在单核细胞/ DC相关生长因子和/或细胞因子的情况下,鼠骨髓来源的谱系阴性细胞中PU.1的过表达诱导CD80和CD86的表达。根据这些结果,我们得出结论,PU.1是CD80和CD86表达的关键因素。我们还发现皮下注射PU.1 siRNA或局部应用乳化乳化的PU.1 siRNA可以有效抑制鼠类接触性超敏反应。我们的结果表明,PU.1是治疗免疫相关疾病的潜在靶标。

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