生物
关贸总协定3
屋尘螨
T辅助细胞
人口
细胞
细胞生物学
流式细胞术
转录因子
免疫学
基因
T细胞
免疫系统
遗传学
过敏
过敏原
医学
环境卫生
作者
Christopher A. Tibbitt,Julian M. Stark,Liesbet Martens,Junjie Ma,Jeff E. Mold,Kim Deswarte,Ganna Oliynyk,Xiaogang Feng,Bart N. Lambrecht,Pieter De Bleser,Susanne Nylén,Hamida Hammad,Marie Arsenian‐Henriksson,Yvan Saeys,Jonathan M. Coquet
出处
期刊:Immunity
[Cell Press]
日期:2019-06-20
卷期号:51 (1): 169-184.e5
被引量:275
标识
DOI:10.1016/j.immuni.2019.05.014
摘要
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.
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