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The Spectrum and Regulatory Landscape of Intestinal Innate Lymphoid Cells Are Shaped by the Microbiome

机译:肠道固有淋巴样细胞的频谱和调控景观是由微生物组塑造的。

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摘要

Innate lymphoid cells (ILCs) are critical modulators of mucosal immunity, inflammation, and tissue homeostasis, but their full spectrum of cellular states and regulatory landscapes remains elusive. Here, we combine genome-wide RNA-seq, ChIP-seq, and ATAC-seq to compare the transcriptional and epigenetic identity of small intestinal ILCs, identifying thousands of distinct gene profiles and regulatory elements. Single-cell RNA-seq and flow and mass cytometry analyses reveal compartmentalization of cytokine expression and metabolic activity within the three classical ILC subtypes and highlight transcriptional states beyond the current canonical classification. In addition, using antibiotic intervention and germ-free mice, we characterize the effect of the microbiome on the ILC regulatory landscape and determine the response of ILCs to microbial colonization at the single-cell level. Together, our work characterizes the spectrum of transcriptional identities of small intestinal ILCs and describes how ILCs differentially integrate signals from the microbial microenvironment to generate phenotypic and functional plasticity.
机译:先天性淋巴样细胞(ILC)是粘膜免疫,炎症和组织动态平衡的关键调节剂,但其完整的细胞状态和调控环境仍然难以捉摸。在这里,我们结合全基因组RNA-seq,ChIP-seq和ATAC-seq来比较小肠ILC的转录和表观遗传同一性,鉴定出数千种不同的基因概况和调控元件。单细胞RNA-seq以及流式细胞和质谱分析揭示了三种经典ILC亚型中细胞因子表达和代谢活性的区室化,并突出了当前规范分类之外的转录状态。此外,使用抗生素干预和无菌小鼠,我们表征了微生物组对ILC调控格局的影响,并确定了ILC对单细胞水平上微生物菌落的响应。总之,我们的工作描述了小肠ILC转录同一性的特征,并描述了ILC如何差异整合微生物微环境的信号以产生表型和功能可塑性。

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