MiRNA profiling of plasma-derived exosomes from dairy cows during gestation

被引:21
|
作者
Zhao, Gan [1 ]
Guo, Shuai [1 ]
Jiang, Kangfeng [1 ]
Zhang, Tao [1 ]
Wu, Haichong [1 ]
Qiu, Changwei [1 ]
Deng, Ganzhen [1 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, Dept Clin Vet Med, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
Pregnancy; Exosomes; miRNAs; RNA-seq; PREGNANCY-ASSOCIATED MICRORNAS; PLACENTAL EXOSOMES; MATERNAL CIRCULATION; EXTRACELLULAR VESICLES; SIGNALING PATHWAY; 1ST TRIMESTER; FETAL; IDENTIFICATION; EXPRESSION; PI3K/AKT;
D O I
10.1016/j.theriogenology.2019.03.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exosomes, one kind of extracellular vesicles, are released under abnormal and normal physiological conditions. An understanding of plasma-derived exosomal microRNA (miRNA) profiles during pregnancy will significantly contribute to knowledge of maternal-fetal communication in ruminants. In this study, we isolated plasma-derived exosomes from dairy cows during early (similar to 60 days, gestational day (G_D) 60), mid (similar to 150 days, G_D 150) and late (similar to 240 days, G_D 240) pregnancy. Exosomal miRNA profiles were revealed using RNA sequencing technology, and the abundance of exosomal miRNAs between each stage were compared. In the G_D150 vs. G_D60, G_D240 vs. G_D60 and G_D240 vs. G_D150stages, there were 23, 32 and 29 miRNAs, respectively, significantly differentially enriched. Significant annotations for protein binding and transport-or immunoregulatory-related categories or pathways were found for the predicted target genes of these miRNAs. In addition, we further identified specific exosomal miRNAs for each pregnancy stage, including the following: bta-miR-499, bta-miR-16a, bta-miR-20a, bta-miR-223, and bta-miR-128 in the G_D60 stage; bta-miR-493, bta-miR-127, and bta-miR-143 in the G_D150 stage; and bta-miR-122, bta-miR-182, bta-miR-183, bta-miR-200b, and bta-miR-200c in the G_D240 stage. Our findings provide new insight into maternal-fetal communication during pregnancy. Future studies will use these data to identify and characterize specific exosomal miRNA regulatory mechanisms in the maternal-fetal immune response. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 98
页数:10
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