对易发坏死性小肠结肠炎期间的产后小肠转录组进行编目。

Luiz Fernando Silva Oliveira, Radhika S Khetani, Yu-Syuan Wu, Venkata Siva Dasuri, Amanda W Harrington, Oluwabunmi Olaloye, Jeffrey Goldsmith, David T Breault, Liza Konnikova, Shannan J Ho Sui, Amy E O'Connell
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引用次数: 0

摘要

在出生后的第一个月,发育中的小鼠肠道从未成熟肠道转变为成熟肠道,这种转变将维持生物体的整个生命周期。在这里,我们通过 RNA-Seq 对 C57Bl/6 小鼠的肠道进行了调查,以评估十二指肠和回肠中的基因表达随着出生后一个月的时间而发生的变化。我们分析了基因表达的变化,发现基因家族的变化与 NEC 易感期或抵抗期相关。我们发现,DNA处理基因和空泡结构基因、组织发育和形态发生基因以及细胞迁移基因的表达增加与NEC易感性相关,而免疫基因组、细胞内转运基因、ATP产生和细胞内代谢基因的表达增加与NEC抵抗性相关。利用 RNA 分析中发现的趋势,我们进一步评估了细胞标志物和上皮调节因子、免疫细胞标志物和腺苷代谢成分的表达。我们通过 qRT-PCR 和免疫荧光确认了关键的变化。此外,我们还利用人类肠道活检组织和器官组织将一些发现与人类进行了比较。该数据集可作为其他研究小组研究单个分子或分子家族在早期肠道和出生后发育中作用的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cataloguing the postnatal small intestinal transcriptome during the first postnatal month.

In the first postnatal month, the developing mouse intestine shifts from an immature to a mature intestine that will sustain the organism throughout the lifespan. Here, we surveyed the mouse intestine in C57Bl/6 mice by RNA-Seq to evaluate the changes in gene expression over time from the day of birth through 1 month of age in both the duodenum and ileum. We analyzed gene expression for changes in gene families that correlated with the periods of NEC susceptibility or resistance. We highlight that increased expression of DNA processing genes and vacuolar structure genes, tissue development and morphogenesis genes, and cell migration genes all correlated with NEC susceptibility, while increases in immunity gene sets, intracellular transport genes, ATP production, and intracellular metabolism genes correlated with NEC resistance. Using trends identified in the RNA-Seq analyses, we further evaluated expression of cellular markers and epithelial regulators, immune cell markers, and adenosine metabolism components. We confirmed key changes with qRT-PCR and immunofluorescence. In addition, we compared some findings to humans using human intestinal biopsies and organoids. This dataset can serve as a reference for other groups considering the role of single molecules or molecular families in early intestinal and postnatal development.

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