1Research Center, Ste-Justine Hospital, 3175 Côte Ste-Catherine, Montréal, QC, Canada, H3T 1C5.
FASEB J. 2014 Apr;28(4):1910-23. doi: 10.1096/fj.13-240168. Epub 2013 Dec 26.
The scavenger receptor CD36 plays a central role in lipid metabolism by promoting macrophage cholesterol efflux with the potential to reduce atherosclerotic lesions. However, the effect of CD36 on de novo cholesterol synthesis is not known. Here, we describe the cellular mechanism by which CD36 activation induces cholesterol depletion in HepG2 cells. Using the CD36 ligand hexarelin, we found a rapid phosphorylation of HMG-CoA reductase Ser-872 in treated cells, resulting in inactivation of the rate-limiting enzyme in sterol synthesis. Degradation of HMG-CoA reductase by the ubiquitin-proteasome pathway was also enhanced by hexarelin, through an increased recruitment of the anchor proteins insulin-induced gene (Insig)-1 and Insig-2. Genes encoding key enzymes involved in cholesterol synthesis and under the control of transcription factor sterol regulatory element-binding protein (SREBP)-2 remained unresponsive to sterol depletion, due to retention of the SREBP-2 escort protein Scap by Insig-1/2. Insig1 and Insig2 gene expression was also increased through activation of nuclear receptor peroxisome-proliferator activating receptor γ (PPARγ) by CD36, which lifted the inhibitory effect of PPARγ1 Ser-84 phosphorylation. Recruitment of coactivator peroxisome proliferator-activated receptor-γ coactivator 1α (PGC1α) to activated AMPKα was also promoted, resulting in PGC-1α transcriptional activation through Sirt1-mediated deacetylation, increased recruitment of PPARγ, and up-regulation of Insig-1/2, revealing a regulatory role of CD36 on PGC-1α signaling. Our data identify CD36 as a novel regulator of HMG-CoA reductase function and Insig-1/2 expression, 2 critical steps regulating cholesterol synthesis in hepatocytes.
清道夫受体 CD36 通过促进巨噬细胞胆固醇外流在脂质代谢中发挥核心作用,有可能减少动脉粥样硬化病变。然而,CD36 对从头合成胆固醇的影响尚不清楚。在这里,我们描述了 CD36 激活诱导 HepG2 细胞胆固醇耗竭的细胞机制。使用 CD36 配体 hexarelin,我们发现处理细胞中 HMG-CoA 还原酶 Ser-872 的快速磷酸化,导致胆固醇合成限速酶失活。通过增加锚蛋白胰岛素诱导基因 (Insig)-1 和 Insig-2 的募集,hexarelin 还增强了 HMG-CoA 还原酶通过泛素-蛋白酶体途径的降解。胆固醇合成关键酶的编码基因受转录因子固醇调节元件结合蛋白 (SREBP)-2 控制,由于 Insig-1/2 保留了 SREBP-2 伴侣蛋白 Scap,因此对胆固醇耗竭无反应。Insig1 和 Insig2 基因表达也通过 CD36 激活核受体过氧化物酶体增殖物激活受体 γ (PPARγ) 而增加,这解除了 PPARγ1 Ser-84 磷酸化的抑制作用。还促进了辅激活因子过氧化物酶体增殖物激活受体-γ 共激活因子 1α (PGC1α) 与激活的 AMPKα 的募集,导致通过 Sirt1 介导的去乙酰化、PPARγ 的募集增加以及 Insig-1/2 的上调来实现 PGC-1α 的转录激活,揭示了 CD36 对 PGC-1α 信号转导的调节作用。我们的数据将 CD36 鉴定为 HMG-CoA 还原酶功能和 Insig-1/2 表达的新型调节剂,这是调节肝细胞胆固醇合成的 2 个关键步骤。