Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario M5B 1T8, Canada.
J Immunol. 2020 Mar 1;204(5):1173-1187. doi: 10.4049/jimmunol.1900744. Epub 2020 Jan 29.
Homogeneous populations of mature differentiated primary cell types can display variable responsiveness to extracellular stimuli, although little is known about the underlying mechanisms that govern such heterogeneity at the level of gene expression. In this article, we show that morphologically homogenous human endothelial cells exhibit heterogeneous expression of VCAM1 after TNF-α stimulation. Variability in VCAM1 expression was not due to stochasticity of intracellular signal transduction but rather to preexisting established heterogeneous states of promoter DNA methylation that were generationally conserved through mitosis. Variability in DNA methylation of the promoter resulted in graded RelA/p65 and RNA polymerase II binding that gave rise to a distribution of transcription in the population after TNF-α stimulation. Microarray analysis and single-cell RNA sequencing revealed that a number of cytokine-inducible genes shared this heterogeneous response pattern. These results show that heritable epigenetic heterogeneity is fundamental in inflammatory signaling and highlight as a metastable epiallele.
成熟分化的原代细胞类型的同质群体对细胞外刺激的反应可能存在差异,尽管对于在基因表达水平上调控这种异质性的潜在机制知之甚少。本文中,我们发现经 TNF-α刺激后,形态上同质的人内皮细胞表现出 VCAM1 的异质性表达。VCAM1 表达的可变性不是由于细胞内信号转导的随机性,而是由于启动子 DNA 甲基化的预先存在的、建立的异质状态,这些状态通过有丝分裂世代保存下来。启动子 DNA 甲基化的可变性导致 RelA/p65 和 RNA 聚合酶 II 结合的分级变化,在 TNF-α刺激后导致转录在群体中的分布。微阵列分析和单细胞 RNA 测序显示,许多细胞因子诱导基因表现出这种异质反应模式。这些结果表明,可遗传的表观遗传异质性是炎症信号转导的基础,并强调 DNA 甲基化为一个亚稳态的表观等位基因。