| Literature DB >> 31231035 |
Christopher Andrew Tibbitt1, Julian Mario Stark1, Liesbet Martens2, Junjie Ma1, Jeff Eron Mold3, Kim Deswarte4, Ganna Oliynyk1, Xiaogang Feng1, Bart Norbert Lambrecht4, Pieter De Bleser2, Susanne Nylén1, Hamida Hammad4, Marie Arsenian Henriksson1, Yvan Saeys5, Jonathan Marie Coquet6.
Abstract
Naive CD4+ T cells differentiate into functionally diverse T helper (Th) cell subsets. Th2 cells play a pathogenic role in asthma, yet a clear picture of their transcriptional profile is lacking. We performed single-cell RNA sequencing (scRNA-seq) of T helper cells from lymph node, lung, and airways in the house dust mite (HDM) model of allergic airway disease. scRNA-seq resolved transcriptional profiles of naive CD4+ T, Th1, Th2, regulatory T (Treg) cells, and a CD4+ T cell population responsive to type I interferons. Th2 cells in the airways were enriched for transcription of many genes, including Cd200r1, Il6, Plac8, and Igfbp7, and their mRNA profile was supported by analysis of chromatin accessibility and flow cytometry. Pathways associated with lipid metabolism were enriched in Th2 cells, and experiments with inhibitors of key metabolic pathways supported roles for glucose and lipid metabolism. These findings provide insight into the differentiation of pathogenic Th2 cells in the context of allergy.Entities:
Keywords: ATAC-seq; T helper; Th2; asthma; house dust mite; interleukin; metabolism; single-cell RNA Sequencing
Year: 2019 PMID: 31231035 DOI: 10.1016/j.immuni.2019.05.014
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745