Department of Experimental Oncology, European Institute of Oncology (IEO), Via Adamello 16, 20139 Milan, Italy.
Philos Trans R Soc Lond B Biol Sci. 2013 May 6;368(1620):20120370. doi: 10.1098/rstb.2012.0370. Print 2013.
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.
在固有免疫系统细胞(如巨噬细胞和树突状细胞)中,针对微生物和危险信号的诱导基因表达程序的部署需要高度精确的调节机制。炎症反应必须根据触发刺激及其剂量进行调整,并且必须以适合炎症过程不同阶段的动力学复杂方式展开。在这种情况下,对调节元件的基因组特征分析表明,参与巨噬细胞特化的转录调节因子作为先驱转录因子(TFs)发挥作用,它们产生开放染色质区域,从而能够招募对外界输入作出反应而被激活的 TFs。因此,对特定刺激的反应能力是由参与谱系决定和细胞身份维持的因子在分化的早期阶段编程的,这些因子负责组织细胞类型特异性顺式调节库。调节固有免疫系统中专业细胞炎症基因表达的基本功能和组织原则,为分化和环境反应之间的相互作用提供了普遍的范例。