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Deciphering cis-regulatory control in inflammatory cells

机译:破解炎症细胞中的顺式调控

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摘要

In innate immune system cells, such as macrophages and dendritic cells, deployment of inducible gene expression programmes in response to microbes and danger signals requires highly precise regulatory mechanisms. The inflammatory response has to be tailored based on both the triggering stimulus and its dose, and it has to be unfolded in a kinetically complex manner that suits the different phases of the inflammatory process. Genomic characterization of regulatory elements in this context indicated that transcriptional regulators involved in macrophage specification act as pioneer transcription factors (TFs) that generate regions of open chromatin that enable the recruitment of TFs activated in response to external inputs. Therefore, competence for responses to a specific stimulus is programmed at an early stage of differentiation by factors involved in lineage commitment and maintenance of cell identity, which are responsible for the organization of a cell-type-specific cis-regulatory repertoire. The basic functional and organizational principles that regulate inflammatory gene expression in professional cells of the innate immune system provide general paradigms on the interplay between differentiation and environmental responses.
机译:在先天免疫系统细胞(例如巨噬细胞和树突状细胞)中,响应微生物和危险信号而部署可诱导基因表达程序需要高度精确的调节机制。必须根据触发刺激及其剂量来调整炎症反应,并且必须以动力学上复杂的方式展开炎症反应,以适应炎症过程的不同阶段。在这种情况下调节元件的基因组表征表明,参与巨噬细胞规范的转录调节剂起先驱转录因子(TFs)的作用,产生开放染色质的区域,这些区域可以募集响应外部输入而激活的TF。因此,在分化的早期,通过参与谱系定型和维持细胞身份的因素来编程对特定刺激的反应能力,这些因素负责组织细胞类型特异性的顺式调控库。调节先天免疫系统专业细胞中炎性基因表达的基本功能和组织原理,为分化和环境反应之间的相互作用提供了一般范式。

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