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肠免疫细胞在新生儿坏死性小肠结肠炎中的单细胞 RNA 测序。

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

机构信息

Department of Pediatric Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Department of Pediatric Surgery, Saitama Medical University, Saitama, Japan.

出版信息

Pediatr Surg Int. 2023 Apr 11;39(1):179. doi: 10.1007/s00383-023-05461-7.

Abstract

PURPOSE

Necrotizing enterocolitis (NEC) causes fatal intestinal necrosis in neonates, but its etiology is unknown. We analyzed the intestinal immune response to NEC.

METHODS

Using 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.

RESULTS

In 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-α, 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.

CONCLUSION

Intestinal 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.

摘要

目的

坏死性小肠结肠炎(NEC)可导致新生儿致命性肠坏死,但病因不明。我们分析了 NEC 的肠道免疫反应。

方法

使用单细胞 RNA 测序(scRNA-seq),我们分析了来自 4 名肠穿孔新生儿(2 名 NEC 和 2 名非 NEC)肠道固有层中肠道免疫细胞的基因表达谱。从切除的肠道固有层中提取目标单核细胞。

结果

在所有 4 例中,主要免疫细胞,如 T 细胞(15.1-47.7%)、B 细胞(3.1-19.0%)、单核细胞(16.5-31.2%)、巨噬细胞(1.6-17.4%)、树突状细胞(2.4-12.2%)和自然杀伤细胞(7.5-12.8%),与新生儿脐带血中的比例相似。基因集富集分析显示,NEC 患者的 T 细胞中 MTOR、TNF-α 和 MYC 信号通路富集,提示与炎症和细胞增殖相关的免疫反应上调。此外,所有 4 例均表现出以细胞介导的炎症为优势,这基于辅助性 T 细胞 1 型的优势。

结论

与非 NEC 患者相比,NEC 患者的肠道免疫表现出更强的炎症反应。进一步的 scRNA-seq 和细胞分析可能有助于我们理解 NEC 的发病机制。

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