小RNA
初乳
免疫系统
生物
微泡
微阵列
外体
微阵列分析技术
计算生物学
免疫学
遗传学
抗体
基因表达
基因
作者
Poonam Verma,Niharika Mohanty,Babita Pruseth,Sonali Sahoo,Amit Katiyar,Harpreet Singh,Saubhagya Kumar Jena,Rashmi Ranjan Das,Tapas Som,Sanjeeb Kumar Sahoo,Pranati Nanda,Amit Ghosh
出处
期刊:MicroRNA
日期:2022-07-04
卷期号:11 (3): 216-226
被引量:4
标识
DOI:10.2174/2211536611666220630102316
摘要
The fetus grows in a sterile womb environment. After birth, the newborn immune system has two immediate hurdles to clear. First immediate suppression of the womb compatible immune system and turn on the immune system of the newborn that can counter the antigenic world. The underlying mechanism of immune fluctuation by milk microRNAs (miRNAs) can be crucial for the treatment of critical or premature newborn.We collected fourteen samples of each colostrum and mature milk from lactating mothers, four samples of each were used for microarray analysis, and the other ten were used for miRNA expression profiling by real-time PCR.From the microarray, 154 differentially expressed miRNAs were identified, whereas 49 miRNAs were revealed as immune-related miRNAs based on a literature study. Among the 49 miRNAs, 33 were already shown as strongly validated immune-related miRNAs (validated by qPCR, Western Blot, and Luciferase assay) and were considered for further analysis. Twenty-two miRNA expressions were analysed by real-time PCR as their Ct values were within considerable limits. Twelve numbers of miRNAs were significantly downregulated in mature milk compared to colostrum, which were again subjected to bioinformatics analysis to predict the biological mechanisms behind the differentially expressed miRNAs.This study shed light on the human milk exosome miRNA expression dynamics during lactation and their possible role in the gradual skewing of the newborns' immune system. The information is crucial for the development and onset of sepsis in premature newborns in the NICU.
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