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本文引用的文献

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MicroRNA modulation of lipid metabolism and oxidative stress in cardiometabolic diseases.微小 RNA 对代谢综合征相关心血管疾病中心血管疾病的脂质代谢和氧化应激的调控作用。
Free Radic Biol Med. 2013 Sep;64:31-9. doi: 10.1016/j.freeradbiomed.2013.07.014. Epub 2013 Jul 17.
2
MicroRNA-144 regulates hepatic ATP binding cassette transporter A1 and plasma high-density lipoprotein after activation of the nuclear receptor farnesoid X receptor.微小 RNA-144 调节核受体法尼醇 X 受体激活后的肝 ATP 结合盒转运蛋白 A1 和血浆高密度脂蛋白。
Circ Res. 2013 Jun 7;112(12):1602-12. doi: 10.1161/CIRCRESAHA.112.300648. Epub 2013 Mar 21.
3
Control of cholesterol metabolism and plasma high-density lipoprotein levels by microRNA-144.miRNA-144 对胆固醇代谢和血浆高密度脂蛋白水平的调控作用。
Circ Res. 2013 Jun 7;112(12):1592-601. doi: 10.1161/CIRCRESAHA.112.300626. Epub 2013 Mar 21.
4
Functional interplay between RNA-binding protein HuR and microRNAs.RNA 结合蛋白 HuR 与 microRNAs 之间的功能相互作用。
Curr Protein Pept Sci. 2012 Jun;13(4):372-9. doi: 10.2174/138920312801619394.
5
Post-transcriptional regulation in metabolic diseases.代谢疾病中的转录后调控。
RNA Biol. 2012 Jun;9(6):772-80. doi: 10.4161/rna.20091. Epub 2012 Jun 1.
6
RNA-binding protein HuD controls insulin translation.RNA 结合蛋白 HuD 控制胰岛素的翻译。
Mol Cell. 2012 Mar 30;45(6):826-35. doi: 10.1016/j.molcel.2012.01.016. Epub 2012 Mar 1.
7
The oncogenic RNA-binding protein Musashi1 is regulated by HuR via mRNA translation and stability in glioblastoma cells.致癌 RNA 结合蛋白 Musashi1 通过 HuR 在神经胶质瘤细胞中的 mRNA 翻译和稳定性进行调节。
Mol Cancer Res. 2012 Jan;10(1):143-55. doi: 10.1158/1541-7786.MCR-11-0208.
8
HuR function in disease.HuR 在疾病中的功能。
Front Biosci (Landmark Ed). 2012 Jan 1;17(1):189-205. doi: 10.2741/3921.
9
MiR-106b impairs cholesterol efflux and increases Aβ levels by repressing ABCA1 expression.miR-106b 通过抑制 ABCA1 的表达来损害胆固醇外排并增加 Aβ 水平。
Exp Neurol. 2012 Jun;235(2):476-83. doi: 10.1016/j.expneurol.2011.11.010. Epub 2011 Nov 18.
10
Genomic analyses of the RNA-binding protein Hu antigen R (HuR) identify a complex network of target genes and novel characteristics of its binding sites.对 RNA 结合蛋白 Hu 抗原 R (HuR) 的基因组分析确定了其靶基因的复杂网络和其结合位点的新特征。
J Biol Chem. 2011 Oct 28;286(43):37063-6. doi: 10.1074/jbc.C111.266882. Epub 2011 Sep 2.

RNA结合蛋白HuR调节ABCA1的表达。

RNA binding protein HuR regulates the expression of ABCA1.

作者信息

Ramírez Cristina M, Lin Chin Sheng, Abdelmohsen Kotb, Goedeke Leigh, Yoon Je-Hyun, Madrigal-Matute Julio, Martin-Ventura Jose L, Vo Dat T, Uren Philip J, Penalva Luiz O, Gorospe Myriam, Fernández-Hernando Carlos

机构信息

Vascular Biology and Therapeutics Program, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06520 Departments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016.

Departments of Medicine and Cell Biology, New York University School of Medicine, New York, NY 10016 Division of Cardiology, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

J Lipid Res. 2014 Jun;55(6):1066-76. doi: 10.1194/jlr.M044925. Epub 2014 Apr 11.

DOI:10.1194/jlr.M044925
PMID:24729624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4031938/
Abstract

ABCA1 is a major regulator of cellular cholesterol efflux and plasma HDL biogenesis. Even though the transcriptional activation of ABCA1 is well established, the posttranscriptional regulation of ABCA1 expression is poorly understood. Here, we investigate the potential contribution of the RNA binding protein (RBP) human antigen R (HuR) on the posttranscriptional regulation of ABCA1 expression. RNA immunoprecipitation assays demonstrate a direct interaction between HuR and ABCA1 mRNA. We found that HuR binds to the 3' untranslated region of ABCA1 and increases ABCA1 translation, while HuR silencing reduces ABCA1 expression and cholesterol efflux to ApoA1 in human hepatic (Huh-7) and monocytic (THP-1) cells. Interestingly, cellular cholesterol levels regulate the expression, intracellular localization, and interaction between HuR and ABCA1 mRNA. Finally, we found that HuR expression was significantly increased in macrophages from human atherosclerotic plaques, suggesting an important role for this RBP in controlling macrophage cholesterol metabolism in vivo. In summary, we have identified HuR as a novel posttranscriptional regulator of ABCA1 expression and cellular cholesterol homeostasis, thereby opening new avenues for increasing cholesterol efflux from atherosclerotic foam macrophages and raising circulat-ing HDL cholesterol levels.

摘要

ABCA1是细胞胆固醇流出和血浆高密度脂蛋白(HDL)生物合成的主要调节因子。尽管ABCA1的转录激活已得到充分证实,但对其表达的转录后调控却知之甚少。在此,我们研究了RNA结合蛋白(RBP)人抗原R(HuR)对ABCA1表达转录后调控的潜在作用。RNA免疫沉淀试验证明HuR与ABCA1 mRNA之间存在直接相互作用。我们发现HuR与ABCA1的3'非翻译区结合并增加ABCA1的翻译,而HuR沉默则降低人肝细胞(Huh-7)和单核细胞(THP-1)中ABCA1的表达以及向载脂蛋白A1的胆固醇流出。有趣的是,细胞胆固醇水平调节HuR与ABCA1 mRNA之间的表达、细胞内定位及相互作用。最后,我们发现人动脉粥样硬化斑块中的巨噬细胞中HuR表达显著增加,表明该RBP在体内控制巨噬细胞胆固醇代谢中起重要作用。总之,我们已确定HuR是ABCA1表达和细胞胆固醇稳态的新型转录后调节因子,从而为增加动脉粥样硬化泡沫巨噬细胞的胆固醇流出及提高循环HDL胆固醇水平开辟了新途径。