STAT6的寡核苷酸捕捞:IL-4和趋化因子之间的串扰

K. W. Eriksen, M. Nielsen, K. Kaltoft, A. Svejgaard, M. H. Nissen, C. Röpke, N. Ødum
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引用次数: 6

摘要

信号转导因子和转录激活因子6 (STAT6)对白细胞介素-4 (IL-4)的生物活性和小鼠过敏反应的发生至关重要。在这里,我们报告了一种敏感和特异性的检测STAT6激活对IL-4的反应。我们利用含有来自免疫球蛋白重链种系Ε转录物启动子的STAT6结合基因序列的双链寡核苷酸探针来研究il -4诱导的STAT6的DNA结合。使用这些探针,我们发现重复相邻的stat6结合位点导致STAT6-DNA结合增强。此外,结合位点之间的距离对于STAT-DNA结合至关重要,即相邻结合位点之间超过20个核苷酸的距离会降低STAT6的结合。通过该实验研究IL-4和趋化因子之间的串扰,我们发现MIP-1β和MIG抑制IL-4诱导的STAT6激活,而其他趋化因子和细胞因子则没有。总之,我们的数据表明,寡核苷酸捕捞是在基因组水平上研究细胞因子串扰的补充工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oligonucleotide Fishing for STAT6: Cross-Talk between IL-4 and Chemokines
Signal transducer and activator of transcription 6 (STAT6) is essential for the biological activities of interleukin-4 (IL-4) and the development of allergic responses in mice. Here we report on a sensitive and specific assay for STAT6 activation in response to IL-4. We took advantage of double-stranded oligonucleotide probes containing a STAT6-binding gene-sequence from the promotor of the immunoglobulin heavy chain germline Ε transcript to study the IL-4-induced DNA binding of STAT6. Using these probes, we show that repeated adjacent STAT6-binding sites result in enhanced STAT6-DNA binding. Moreover, the distance between the binding sites is critical for STAT-DNA binding, i.e. STAT6 binding is decreased at distances above 20 nucleotides between neighbouring binding sites. Using this assay to study cross-talk between IL-4 and chemokines, we provide evidence that MIP-1β and MIG inhibit IL-4-induced STAT6 activation, whereas other chemokines and cytokines do not. In conclusion, our data show that oligonucleotide fishing is a supplementary tool for studying cytokine cross-talk at a genomic level.
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