RNA测序揭示受分娩方式影响的脐带血中的基因表达和通路特征。

IF 3.7 Q2 GENETICS & HEREDITY
Phenomics (Cham, Switzerland) Pub Date : 2023-04-08 eCollection Date: 2023-06-01 DOI:10.1007/s43657-022-00086-7
Yongjie Liu, Kun Sun, Yuexin Gan, Han Liu, Juehua Yu, Wei Xu, Lin Zhang, Dan Chen
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引用次数: 0

摘要

剖腹产会增加后代患I型糖尿病、哮喘、炎症性肠病、乳糜泻、超重和肥胖等的风险。然而,其根本机制仍然未知。为了研究CS对脐血中基因表达的影响,我们对8名选择性CS出生的足月婴儿和8名匹配的阴道分娩(VD)婴儿进行了RNA测序,然后进行了单基因分析、基因集富集分析、基因共表达网络分析和相互作用基因/蛋白质分析。在另外20名CS和20名VD婴儿中进一步验证了上述关键基因。我们首次发现,CS对参与免疫反应(IL12A、INFG、IL1B、TNF、MIF、IL4、CA1、IFI27、HLA-DOB和EPHB1)和代谢(DLK1、CYP2A6和GATM)的基因的mRNA表达有显著影响。值得注意的是,CS婴儿血清TNF-α和IFN-γ显著上调(p = 5 × 10-4和3.0 × 10-3)。CS可能通过影响上述过程中基因的表达,对后代健康产生不利影响,这在生物学上是合理的。这些发现将有助于了解CS对健康不利影响的潜在潜在潜在机制,并确定不同分娩方式出生的后代未来健康的生物标志物。补充信息:在线版本包含补充材料,请访问10.1007/s43657-022-00086-7。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA-Sequencing Reveals Gene Expression and Pathway Signatures in Umbilical Cord Blood Affected by Birth Delivery Mode.

Cesarean section (CS) confers increased risk of type I diabetes, asthma, inflammatory bowel disease, celiac disease, overweight and obesity, etc., in the offspring. However, the underlying mechanism remains unknown. To investigate the influence of CS on gene expression in cord blood, we have performed RNA-sequencing followed by single-gene analysis, gene set enrichment analysis, gene co-expression network analysis, and interacting genes/proteins analysis in eight full-term infants born by elective CS and eight matched vaginally delivered (VD) infants. Crucial genes identified above were further validated in another 20 CS and 20 VD infants. We found for the first time that mRNA expression of genes involved in immune response (IL12A, INFG, IL1B, TNF, MIF, IL4, CA1, IFI27, HLA-DOB and EPHB1) and metabolism (DLK1, CYP2A6 and GATM) were significantly influenced by CS. Notably, serum TNF-α and IFN-γ were remarkably up-regulated in the CS infants (p = 5.0 × 10-4 and 3.0 × 10-3, respectively) compared to the VD infants. It is biologically plausible that CS may exert adverse impacts on offspring health through influencing expression of genes in the above processes. These findings will help understand the potential underlying mechanisms of the adverse health impacts of CS and identify biomarkers for future health of offspring born with different delivery modes.

Supplementary information: The online version contains supplementary material available at 10.1007/s43657-022-00086-7.

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