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本文引用的文献

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Metazoan MicroRNAs.后生动物 MicroRNAs。
Cell. 2018 Mar 22;173(1):20-51. doi: 10.1016/j.cell.2018.03.006.
2
Genetic Ablation of miR-33 Increases Food Intake, Enhances Adipose Tissue Expansion, and Promotes Obesity and Insulin Resistance.miR-33 基因缺失可增加食物摄入、增强脂肪组织扩张,并促进肥胖和胰岛素抵抗。
Cell Rep. 2018 Feb 20;22(8):2133-2145. doi: 10.1016/j.celrep.2018.01.074.
3
Genetic Dissection of the Impact of miR-33a and miR-33b during the Progression of Atherosclerosis.miR-33a 和 miR-33b 在动脉粥样硬化进展过程中影响的遗传剖析。
Cell Rep. 2017 Oct 31;21(5):1317-1330. doi: 10.1016/j.celrep.2017.10.023.
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MicroRNAs and lipid metabolism.微小RNA与脂质代谢
Curr Opin Lipidol. 2017 Jun;28(3):273-280. doi: 10.1097/MOL.0000000000000420.
5
Long-term therapeutic silencing of miR-33 increases circulating triglyceride levels and hepatic lipid accumulation in mice.长期抑制小鼠体内的miR-33会导致其循环甘油三酯水平升高和肝脏脂质蓄积。
EMBO Mol Med. 2014 Sep;6(9):1133-41. doi: 10.15252/emmm.201404046.
6
MicroRNA-33 regulates sterol regulatory element-binding protein 1 expression in mice.MicroRNA-33 调控小鼠固醇调节元件结合蛋白 1 的表达。
Nat Commun. 2013;4:2883. doi: 10.1038/ncomms3883.
7
Pharmacological inhibition of a microRNA family in nonhuman primates by a seed-targeting 8-mer antimiR.通过一种靶向种子的 8 个碱基的反 miRNA 抑制非人灵长类动物中的 microRNA 家族。
Sci Transl Med. 2013 Nov 20;5(212):212ra162. doi: 10.1126/scitranslmed.3006840.
8
MicroRNAs in metabolism and metabolic disorders.微小 RNA 在代谢和代谢紊乱中的作用。
Nat Rev Mol Cell Biol. 2012 Mar 22;13(4):239-50. doi: 10.1038/nrm3313.
9
Inhibition of miR-33a/b in non-human primates raises plasma HDL and lowers VLDL triglycerides.在非人类灵长类动物中抑制 miR-33a/b 可提高血浆高密度脂蛋白胆固醇并降低极低密度脂蛋白甘油三酯。
Nature. 2011 Oct 19;478(7369):404-7. doi: 10.1038/nature10486.

miR-33:代谢之谜。

miR-33: A Metabolic Conundrum.

机构信息

Harvard Medical School and Massachusetts General Hospital Cancer Center, Building 149, 13th Street, Charlestown, MA, USA.

出版信息

Trends Endocrinol Metab. 2018 Oct;29(10):667-668. doi: 10.1016/j.tem.2018.04.004. Epub 2018 Apr 21.

DOI:10.1016/j.tem.2018.04.004
PMID:29692333
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6151149/
Abstract

The miR-33 microRNAs (miRNAs) are crucial regulators of cholesterol/lipids, and may represent therapeutic targets for the treatment of atherosclerosis. A recent report by Price et al. showed that miR-33 knockout (KO) mice exhibit obesity, insulin resistance, and increased food intake, suggesting that metabolic regulation by miR-33 is more complex than was previously known.

摘要

miR-33 微 RNA(miRNAs)是胆固醇/脂质的关键调节因子,可能代表了动脉粥样硬化治疗的治疗靶点。Price 等人的最近报告表明,miR-33 敲除(KO)小鼠表现出肥胖、胰岛素抵抗和食物摄入增加,这表明 miR-33 的代谢调节比以前所知的更为复杂。