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

被引:484
作者
Gury-BenAri, Meital [1 ]
Thaiss, Christoph A. [1 ]
Serafini, Nicolas [2 ,3 ]
Winter, Deborah R. [1 ]
Giladi, Amir [1 ]
Lara-Astiaso, David [1 ]
Levy, Maayan [1 ]
Salame, Tomer Meir [4 ]
Weiner, Assaf [1 ]
David, Eyal [1 ]
Shapiro, Hagit [1 ]
Dori-Bachash, Mally [1 ]
Pevsner-Fischer, Meirav [1 ]
Lorenzo-Vivas, Erika [1 ]
Keren-Shaul, Hadas [1 ]
Paul, Franziska [1 ]
Harmelin, Alon [5 ]
Eberl, Gerard [6 ,7 ]
Itzkovitz, Shalev [8 ]
Tanay, Amos [9 ,10 ]
Di Santo, James P. [2 ,3 ]
Elinav, Eran [1 ]
Amit, Ido [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Inst Pasteur, Innate Immun Unit, F-75015 Paris, France
[3] INSERM, U1223, Paris, France
[4] Weizmann Inst Sci, Biol Serv Unit, IL-76100 Rehovot, Israel
[5] Weizmann Inst Sci, Dept Vet Resources, IL-76100 Rehovot, Israel
[6] Inst Pasteur, Dept Immunol, F-75015 Paris, France
[7] CNRS, URA 1961, F-75015 Paris, France
[8] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[9] Weizmann Inst Sci, Dept Comp Sci & Appl Math, IL-76100 Rehovot, Israel
[10] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
基金
以色列科学基金会; 欧洲研究理事会;
关键词
TRANSCRIPTION FACTOR GATA3; ROR-GAMMA-T; RNA-SEQ; FUNCTIONAL PLASTICITY; COMMENSAL MICROFLORA; NKP46(+) CELLS; INFLAMMATION; HOMEOSTASIS; FATE; DIFFERENTIATION;
D O I
10.1016/j.cell.2016.07.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
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.
引用
收藏
页码:1231 / +
页数:29
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