Single-cell atlas of the human neonatal small intestine affected by necrotizing enterocolitis

被引:10
|
作者
Egozi, Adi [1 ]
Olaloye, Oluwabunmi W. [2 ]
Werner, Lael [3 ,4 ]
Silva, Tatiana [2 ]
McCourt, Blake [2 ]
Pierce, Richard S. [2 ,5 ]
An, Xiaojing [6 ]
Wang, Fujing [6 ]
Chen, Kong [6 ]
Pober, Jordan [5 ,7 ]
Shouval, Dror [3 ,4 ]
Itzkovitz, Shalev [1 ]
Konnikova, Liza [2 ,5 ,8 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, Rehovot, Israel
[2] Yale Sch Med, Dept Pediat, New Haven, CT 06510 USA
[3] Edmond & Lily Safra Childrens Hosp Sheba Med Ctr R, Pediat Gastroenterol Unit, Ramat Gan, Israel
[4] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[5] Yale Sch Med, Program Human & Translat Immunol, New Haven, CT 06510 USA
[6] Univ Pittsburgh, Dept Med, Montefiore Hosp, Med Ctr, Pittsburgh, PA USA
[7] Yale Sch Med, Dept Immunobiol, New Haven, CT USA
[8] Yale Sch Med, Dept Obstet, Gynecol & Reprod Sci, New Haven, CT 06510 USA
基金
欧洲研究理事会; 以色列科学基金会;
关键词
REGULATORY T-CELLS; MAINTENANCE THERAPY; GENE-EXPRESSION; IFN-GAMMA; INFLAMMATION; PATHOGENESIS; MACROPHAGES; VEDOLIZUMAB; CHEMOKINES; RECEPTORS;
D O I
10.1371/journal.pbio.3002124
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 (TCR beta) 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 TCR beta 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.
引用
收藏
页数:29
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