Single-cell RNA sequencing of intestinal immune cells in neonatal necrotizing enterocolitis

被引:1
|
作者
Oshima, Kazuo [1 ,2 ]
Hinoki, Akinari [1 ]
Uchida, Hiroo [1 ]
Tanaka, Yujiro [1 ,2 ]
Okuno, Yusuke [3 ]
Go, Yasuhiro [4 ,5 ,6 ]
Shirota, Chiyoe [1 ]
Tainaka, Takahisa [1 ]
Sumida, Wataru [1 ]
Yokota, Kazuki [1 ]
Makita, Satoshi [1 ]
Takimoto, Aitaro [1 ]
Kano, Yoko [1 ]
Sawa, Shinichiro [7 ]
机构
[1] Nagoya Univ, Grad Sch Med, Dept Pediat Surg, Nagoya, Japan
[2] Saitama Med Univ, Dept Pediat Surg, Moroyama, Saitama, Japan
[3] Nagoya City Univ, Grad Sch Med Sci, Dept Virol, Nagoya, Japan
[4] Natl Inst Nat Sci, Exploratory Res Ctr Life & Living Syst ExCELLS, Cognit Genom Res Grp, Okazaki, Japan
[5] Natl Inst Physiol Sci, Dept Syst Neurosci, Okazaki, Japan
[6] SOKENDAI Grad Univ Adv Studies, Sch Life Sci, Dept Physiol Sci, Okazaki, Japan
[7] Kyushu Univ, Res Ctr Syst Immunol, Div Mucosal Immunol, 3-1-1 Maidashi, Higashi Ku, Fukuoka 8128582, Japan
关键词
Necrotizing enterocolitis; Single-cell sequencing; Intestinal immune cells; Gene expression; T-CELLS; DIFFERENTIATION; PERFORATION; MONOCYTE; SUBSETS; INNATE; MEMORY;
D O I
10.1007/s00383-023-05461-7
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
PurposeNecrotizing enterocolitis (NEC) causes fatal intestinal necrosis in neonates, but its etiology is unknown. We analyzed the intestinal immune response to NEC.MethodsUsing single-cell RNA sequencing (scRNA-seq), we analyzed the gene expression profiles of intestinal immune cells from four neonates with intestinal perforation (two with NEC and two without NEC). Target mononuclear cells were extracted from the lamina propria of the resected intestines.ResultsIn all four cases, major immune cells, such as T cells (15.1-47.7%), B cells (3.1-19.0%), monocytes (16.5-31.2%), macrophages (1.6-17.4%), dendritic cells (2.4-12.2%), and natural killer cells (7.5-12.8%), were present in similar proportions to those in the neonatal cord blood. Gene set enrichment analysis showed that the MTOR, TNF-alpha, and MYC signaling pathways were enriched in T cells of the NEC patients, suggesting upregulated immune responses related to inflammation and cell proliferation. In addition, all four cases exhibited a bias toward cell-mediated inflammation, based on the predominance of T helper 1 cells.ConclusionIntestinal immunity in NEC subjects exhibited stronger inflammatory responses compared to non-NEC subjects. Further scRNA-seq and cellular analysis may improve our understanding of the pathogenesis of NEC.
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页数:10
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