Higashi Yusuke, Sukhanov Sergiy, Parthasarathy Sampath, Delafontaine Patrice
Section of Cardiology, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Am J Physiol Heart Circ Physiol. 2008 Oct;295(4):H1684-9. doi: 10.1152/ajpheart.00548.2008. Epub 2008 Aug 22.
Oxidized low-density lipoprotein (LDL) is proatherogenic and induces smooth muscle cell apoptosis, which contributes to atherosclerotic plaque destabilization. We showed previously that oxidized LDL downregulates insulin-like growth factor-1 receptor in human smooth muscle cells and that this is critical for induction of apoptosis. To identify mechanisms, we exposed smooth muscle cells to 60 mug/ml oxidized LDL or native LDL and assessed insulin-like growth factor-1 receptor mRNA levels, protein synthesis rate, and receptor protein stability. Oxidized LDL decreased insulin-like growth factor-1 receptor mRNA levels by 30% at 8 h compared with native LDL, and this decrease was maintained for up to 20 h. However, insulin-like growth factor-1 receptor protein synthesis rate was not altered by oxidized LDL. Pulse-chase labeling experiments revealed that oxidized LDL reduced insulin-like growth factor-1 receptor protein half-life to 12.2+/-1.7 h from 24.4+/-4.7 h with native LDL. This destabilization of insulin-like growth factor-1 receptor protein was accompanied by enhanced receptor ubiquitination. Overexpression of dominant-negative Nedd4 prevented oxidized LDL-induced downregulation of insulin-like growth factor-1 receptor, suggesting that Nedd4 was the ubiquitin ligase that mediated receptor downregulation. However, the proteasome inhibitors lactacystin, MG-132, and proteasome inhibitor-1 failed to block oxidized LDL-induced downregulation of insulin-like growth factor-1 receptor. Thus oxidized LDL downregulates insulin-like growth factor-1 receptor by destabilizing the protein via Nedd4-enhanced ubiquitination, leading to degradation via a proteasome-independent pathway. This finding provides novel insights into oxidized LDL-triggered oxidant signaling and mechanisms of smooth muscle cell depletion that contribute to plaque destabilization and coronary events.
氧化型低密度脂蛋白(LDL)具有促动脉粥样硬化作用,并可诱导平滑肌细胞凋亡,这会导致动脉粥样硬化斑块不稳定。我们之前表明,氧化型LDL可下调人平滑肌细胞中的胰岛素样生长因子-1受体,而这对于诱导细胞凋亡至关重要。为了确定其机制,我们将平滑肌细胞暴露于60μg/ml的氧化型LDL或天然LDL中,并评估胰岛素样生长因子-1受体的mRNA水平、蛋白质合成速率和受体蛋白稳定性。与天然LDL相比,氧化型LDL在8小时时使胰岛素样生长因子-1受体mRNA水平降低了30%,并且这种降低持续了长达20小时。然而,氧化型LDL并未改变胰岛素样生长因子-1受体的蛋白质合成速率。脉冲追踪标记实验表明,氧化型LDL使胰岛素样生长因子-1受体蛋白的半衰期从天然LDL的24.4±4.7小时缩短至12.2±1.7小时。胰岛素样生长因子-1受体蛋白的这种不稳定伴随着受体泛素化增强。显性负性Nedd4的过表达可阻止氧化型LDL诱导的胰岛素样生长因子-1受体下调,这表明Nedd4是介导受体下调的泛素连接酶。然而,蛋白酶体抑制剂乳胞素、MG-132和蛋白酶体抑制剂-1未能阻断氧化型LDL诱导的胰岛素样生长因子-1受体下调。因此,氧化型LDL通过Nedd4增强的泛素化使蛋白质不稳定来下调胰岛素样生长因子-1受体,导致通过蛋白酶体非依赖途径降解。这一发现为氧化型LDL触发的氧化信号以及平滑肌细胞耗竭的机制提供了新的见解,这些机制有助于斑块不稳定和冠状动脉事件。