From the Department of Neurology, Huashan Hospital, Fudan University, Shanghai 200032, China,; the Department of Neuroscience, Mayo Clinic, Jacksonville, Florida 32224, and.
the Department of Neuroscience, Mayo Clinic, Jacksonville, Florida 32224, and.
J Biol Chem. 2014 Apr 18;289(16):11282-11292. doi: 10.1074/jbc.M113.526095. Epub 2014 Mar 5.
Apolipoprotein E (apoE) is the major cholesterol transport protein in the brain. Among the three human APOE alleles (APOE2, APOE3, and APOE4), APOE4 is the strongest genetic risk factor for late-onset Alzheimer disease (AD). The accumulation of amyloid-β (Aβ) is a central event in AD pathogenesis. Increasing evidence demonstrates that apoE isoforms differentially regulate AD-related pathways through both Aβ-dependent and -independent mechanisms; therefore, modulating apoE secretion, lipidation, and function might be an attractive approach for AD therapy. We performed a drug screen for compounds that modulate apoE production in immortalized astrocytes derived from apoE3-targeted replacement mice. Here, we report that retinoic acid (RA) isomers, including all-trans-RA, 9-cis-RA, and 13-cis-RA, significantly increase apoE secretion to ~4-fold of control through retinoid X receptor (RXR) and RA receptor. These effects on modulating apoE are comparable with the effects recently reported for the RXR agonist bexarotene. Furthermore, all of these compounds increased the expression of the cholesterol transporter ABCA1 and ABCG1 levels and decreased cellular uptake of Aβ in an apoE-dependent manner. Both bexarotene and 9-cis-RA promote the lipidation status of apoE, in which 9-cis-RA promotes a stronger effect and exhibits less cytotoxicity compared with bexarotene. Importantly, we showed that oral administration of bexarotene and 9-cis-RA significantly increases apoE, ABCA1, and ABCG1 levels in mouse brains. Taken together, our results demonstrate that RXR/RA receptor agonists, including several RA isomers, are effective modulators of apoE secretion and lipidation and may be explored as potential drugs for AD therapy.
载脂蛋白 E(apoE)是大脑中主要的胆固醇转运蛋白。在人类的三个 APOE 等位基因(APOE2、APOE3 和 APOE4)中,APOE4 是晚发性阿尔茨海默病(AD)最强的遗传风险因素。淀粉样蛋白-β(Aβ)的积累是 AD 发病机制中的一个核心事件。越来越多的证据表明,apoE 异构体通过 Aβ 依赖和非依赖机制,差异调节 AD 相关途径;因此,调节 apoE 的分泌、脂质化和功能可能是 AD 治疗的一种有吸引力的方法。我们对从 apoE3 靶向替换小鼠衍生的永生化星形胶质细胞中调节 apoE 产生的化合物进行了药物筛选。在这里,我们报告视黄酸(RA)异构体,包括全反式 RA、9-顺式 RA 和 13-顺式 RA,通过视黄酸 X 受体(RXR)和 RA 受体显著增加 apoE 的分泌,达到对照的约 4 倍。这些调节 apoE 的作用与最近报道的 RXR 激动剂贝沙罗汀的作用相当。此外,所有这些化合物都以 apoE 依赖的方式增加了胆固醇转运蛋白 ABCA1 和 ABCG1 的表达,并减少了 Aβ 的细胞摄取。贝沙罗汀和 9-顺式 RA 均促进 apoE 的脂质化状态,其中 9-顺式 RA 比贝沙罗汀促进更强的效果,且细胞毒性较小。重要的是,我们表明贝沙罗汀和 9-顺式 RA 的口服给药可显著增加小鼠大脑中的 apoE、ABCA1 和 ABCG1 水平。总之,我们的研究结果表明,RXR/RA 受体激动剂,包括几种 RA 异构体,是 apoE 分泌和脂质化的有效调节剂,可能被探索作为 AD 治疗的潜在药物。