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餐后循环 miRNA 对膳食脂肪挑战的响应。

Postprandial Circulating miRNAs in Response to a Dietary Fat Challenge.

机构信息

Laboratory of Epigenetics of Lipid Metabolism, Madrid Institute for Advanced Studies (IMDEA)-Food, CEI UAM + CSIC, 28049 Madrid, Spain.

Laboratory of Functional Foods, Madrid Institute for Advanced Studies (IMDEA)-Food, CEI UAM + CSIC, 28049 Madrid, Spain.

出版信息

Nutrients. 2019 Jun 13;11(6):1326. doi: 10.3390/nu11061326.

DOI:10.3390/nu11061326
PMID:31200481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6627817/
Abstract

Postprandial lipemia has many physiopathological effects, some of which increase the risk of cardiovascular disease. MicroRNAs (miRNAs) can be found in almost all biological fluids, but their postprandial kinetics are poorly described. We aimed to profile circulating miRNAs in response to a fat challenge. In total, 641 circulating miRNAs were assessed by real-time PCR in plasmas from mice two hours after lipid gavage. Mice with intestine-specific loss of Dicer were screened to identify potential miRNAs released by the intestine. A total of 68 miRNAs were selected for further validation. Ten circulating miRNAs were finally validated as responsive to postprandial lipemia, including miR-206-3p, miR-543-3p, miR-466c-5p, miR-27b-5p, miR-409-3p, miR-340-3p, miR-1941-3p, miR-10a-3p, miR-125a-3p, and miR-468-3p. Analysis of their possible tissues of origin/target showed an enrichment of selected miRNAs in liver, intestine, brain, or skeletal muscle. miR-206, miR-27b-5p, and miR-409-3p were validated in healthy humans. Analysis of their predicted target genes revealed their potential involvement in insulin/insulin like growth factor (insulin/IGF), angiogenesis, cholecystokinin B receptor signaling pathway (CCKR), inflammation or Wnt pathways for mice, and in platelet derived growth factor (PDGF) and CCKR signaling pathways for humans. Therefore, the current study shows that certain miRNAs are released in the circulation in response to fatty meals, proposing them as potential novel therapeutic targets of lipid metabolism.

摘要

餐后血脂异常有许多生理病理作用,其中一些会增加心血管疾病的风险。microRNAs(miRNAs)几乎存在于所有生物体液中,但它们的餐后动力学特征描述得很差。我们旨在研究脂肪刺激后循环 miRNA 的特征。我们通过实时 PCR 检测了脂餐后两小时小鼠血浆中 641 种循环 miRNA。筛选肠特异性缺失 Dicer 的小鼠,以鉴定潜在的由肠道释放的 miRNA。共选择了 68 个 miRNA 进行进一步验证。最终有 10 个循环 miRNA 被验证对餐后血脂异常有反应,包括 miR-206-3p、miR-543-3p、miR-466c-5p、miR-27b-5p、miR-409-3p、miR-340-3p、miR-1941-3p、miR-10a-3p、miR-125a-3p 和 miR-468-3p。对其可能的组织起源/靶位的分析表明,选定的 miRNA 在肝脏、肠道、大脑或骨骼肌中富集。miR-206、miR-27b-5p 和 miR-409-3p 在健康人中得到验证。对其预测靶基因的分析表明,它们可能参与胰岛素/胰岛素样生长因子(胰岛素/IGF)、血管生成、胆囊收缩素 B 受体信号通路(CCKR)、炎症或 Wnt 通路(对小鼠)和血小板衍生生长因子(PDGF)和 CCKR 信号通路(对人)。因此,本研究表明,某些 miRNA 会在脂肪餐后释放到循环中,这为脂质代谢的潜在新治疗靶点提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/e81dae34604f/nutrients-11-01326-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/8eb7b33e8970/nutrients-11-01326-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/2a9f1fe1b45d/nutrients-11-01326-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/11117685071c/nutrients-11-01326-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/1e4e2d0116c3/nutrients-11-01326-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/d75c12f2295a/nutrients-11-01326-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/e81dae34604f/nutrients-11-01326-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/8eb7b33e8970/nutrients-11-01326-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/2a9f1fe1b45d/nutrients-11-01326-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/11117685071c/nutrients-11-01326-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/1e4e2d0116c3/nutrients-11-01326-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/d75c12f2295a/nutrients-11-01326-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41a9/6627817/e81dae34604f/nutrients-11-01326-g006.jpg

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