Influence of technical and maternal-infant factors on the measurement and expression of extracellular miRNA in human milk

小RNA 细胞外 表达式(计算机科学) 生物 细胞外小泡 细胞生物学 计算生物学 医学 遗传学 计算机科学 基因 程序设计语言
作者
Elizabeth A. Holzhausen,Allison Kupsco,Bridget Chalifour,William B. Patterson,Kelsey A. Schmidt,Pari Mokhtari,Andrea Baccarelli,Michael I. Goran,Tanya L. Alderete
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:14 被引量:6
标识
DOI:10.3389/fimmu.2023.1151870
摘要

Breast milk contains thousands of bioactive compounds including extracellular vesicle microRNAs (EV-miRNAs), which may regulate pathways such as infant immune system development and metabolism. We examined the associations between the expression of EV-miRNAs and laboratory variables (i.e., batch effects, sample characteristics), sequencing quality indicators, and maternal-infant characteristics. The study included 109 Latino mother-infant dyads from the Southern California Mother's Milk Study. Mothers were age 28.0 ± 5.6 and 23-46 days postpartum. We used principal components analysis to evaluate whether EV-miRNA expression was associated with factors of interest. Then, we used linear models to estimate relationships between these factors and specific EV-miRNA counts and analyzed functional pathways associated with those EV-miRNAs. Finally, we explored which maternal-infant characteristics predicted sequencing quality indicators. Sequencing quality indicators, predominant breastfeeding, and breastfeedings/day were associated with EV-miRNA principal components. Maternal body mass index and breast milk collection timing predicted proportion of unmapped reads. Expression of 2 EV-miRNAs were associated with days postpartum, 23 EV-miRNAs were associated with breast milk collection time, 23 EV-miRNAs were associated with predominant breastfeeding, and 38 EV-miRNAs were associated with breastfeedings/day. These EV-miRNAs were associated with pathways including Hippo signaling pathway and ECM-receptor interaction, among others. This study identifies several important factors that may contribute to breast milk EV-miRNA expression. Future studies should consider these findings in the design and analysis of breast milk miRNA research.

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