坏死性小肠结肠炎
生物
地图集(解剖学)
小肠
解剖
内科学
医学
内分泌学
作者
Adi Egozi,Oluwabunmi Olaloye,Lael Werner,Tatiana Silva,Blake McCourt,Richard W. Pierce,Xiaojing An,Fujing Wang,Kong Chen,Jordan S. Pober,Dror S. Shouval,Shalev Itzkovitz,Liza Konnikova
出处
期刊:PLOS Biology
[Public Library of Science]
日期:2023-05-19
卷期号:21 (5): e3002124-e3002124
被引量:42
标识
DOI:10.1371/journal.pbio.3002124
摘要
Necrotizing enterocolitis (NEC) is a gastrointestinal complication of premature infants with high rates of morbidity and mortality. A comprehensive view of the cellular changes and aberrant interactions that underlie NEC is lacking. This study aimed at filling in this gap. We combine single-cell RNA sequencing (scRNAseq), T-cell receptor beta (TCRβ) analysis, bulk transcriptomics, and imaging to characterize cell identities, interactions, and zonal changes in NEC. We find an abundance of proinflammatory macrophages, fibroblasts, endothelial cells as well as T cells that exhibit increased TCRβ clonal expansion. Villus tip epithelial cells are reduced in NEC and the remaining epithelial cells up-regulate proinflammatory genes. We establish a detailed map of aberrant epithelial-mesenchymal-immune interactions that are associated with inflammation in NEC mucosa. Our analyses highlight the cellular dysregulations of NEC-associated intestinal tissue and identify potential targets for biomarker discovery and therapeutics.
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