生物
先天性淋巴细胞
微生物群
免疫学
先天免疫系统
计算生物学
免疫系统
细胞生物学
遗传学
作者
Meital Gury-BenAri,Christoph A. Thaiss,Nicolas Serafini,Deborah R. Winter,Amir Giladi,David Lara‐Astiaso,Maayan Levy,Tomer Meir Salame,Assaf Weiner,Eyal David,Hagit Shapiro,Mally Dori-Bachash,Meirav Pevsner‐Fischer,Erika Lorenzo-Vivas,Hadas Keren‐Shaul,Franziska Paul,Alon Harmelin,Gérard Eberl,Shalev Itzkovitz,Amos Tanay
出处
期刊:Cell
[Cell Press]
日期:2016-08-01
卷期号:166 (5): 1231-1246.e13
被引量:525
标识
DOI:10.1016/j.cell.2016.07.043
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.
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