| Literature DB >> 27545347 |
Meital Gury-BenAri1, Christoph A Thaiss1, Nicolas Serafini2, Deborah R Winter1, Amir Giladi1, David Lara-Astiaso1, Maayan Levy1, Tomer Meir Salame3, Assaf Weiner1, Eyal David1, Hagit Shapiro1, Mally Dori-Bachash1, Meirav Pevsner-Fischer1, Erika Lorenzo-Vivas1, Hadas Keren-Shaul1, Franziska Paul1, Alon Harmelin4, Gérard Eberl5, Shalev Itzkovitz6, Amos Tanay7, James P Di Santo2, Eran Elinav8, Ido Amit9.
Abstract
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.Entities:
Keywords: epigenome; innate lymphoid cells; microbiota; single-cell transcriptomics
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Year: 2016 PMID: 27545347 DOI: 10.1016/j.cell.2016.07.043
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582