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