致动脉粥样硬化饮食加速弹性假黄瘤小鼠模型的异位矿化。

Jing-Yi Zhao, Joshua Kingman, Ida Joely Jacobs, Jouni Uitto, Yi Cao, Qiao-Li Li
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引用次数: 1

摘要

目的:弹性假黄瘤(PXE)是一种由Abcc6基因突变引起的多系统遗传性疾病。这种疾病的特征是皮肤、眼睛和动脉血管的异位矿化。先前的研究表明PXE患者的心血管并发症部分是由过早的动脉粥样硬化引起的。本研究的目的是确定致动脉粥样硬化饮食对异位矿化的影响。方法:以Abcc6 tm1JfK小鼠(Abcc6 -/-小鼠)作为PXE的临床前模型。4周龄子代分为两组,分别饲喂实验室标准对照饲料(对照组)和致动脉粥样硬化饲料。测定血清脂质和胆汁酸,分别用组织病理学分析和化学钙定量法评价脂肪变性和组织矿化。结果:致动脉粥样硬化饮食50 ~ 58周后,致动脉粥样硬化饮食组Abcc6 -/-小鼠的总胆固醇、低密度脂蛋白/极低密度脂蛋白胆固醇和胆汁酸浓度(分别为180.9±14.8 g/L、145.9±12.9 g/L和9.7±1.4 μmol/L)显著高于对照组Abcc6 -/-小鼠(分别为85.2±4.8 g/L、25.1±5.5 g/L和3.3±0.5 μmol/L) (P P P)。这些观察结果表明,致动脉粥样硬化饮食导致Abcc6 -/-小鼠高胆固醇血症和加速异位矿化。我们的研究结果对PXE患者具有临床意义,PXE是一种目前难治性疾病,具有相当高的发病率和偶尔的死亡率。
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Atherogenic Diet Accelerates Ectopic Mineralization in a Mouse Model of Pseudoxanthoma Elasticum.

Objective: Pseudoxanthoma elasticum (PXE) is a multisystem heritable disorder caused by mutations in the Abcc6 gene. The disease is characterized by ectopic mineralization of the skin, eyes, and arterial blood vessels. Previous studies have suggested that cardiovascular complications in patients with PXE are caused in part by premature atherosclerosis. The aim of this study is to determine the effect of an atherogenic diet on ectopic mineralization.

Methods: We used Abcc6 tm1JfK mice (Abcc6 -/- mice) as an established preclinical model of PXE. The offspring at age of 4 weeks were divided into two groups and fed the standard control laboratory diet (control group) and the atherogenic diet. Serum lipid profiles and bile acids were measured, and steatosis and tissue mineralization were evaluated by histopathologic analysis and chemical calcium quantification assay, respectively.

Results: After 50-58 weeks of feeding an atherogenic diet, the concentrations of total cholesterol, low-density lipoprotein/very-low-density lipoprotein cholesterol, and bile acids were significantly higher in the Abcc6 -/- mice on the atherogenic diet (180.9 ± 14.8 g/L, 145.9 ± 12.9 g/L, and 9.7 ± 1.4 μmol/L, respectively) than in Abcc6 -/- mice on a control diet (85.2 ± 4.8 g/L, 25.1 ± 5.5 g/L, and 3.3 ± 0.5 μmol/L, respectively) (P < 0.001). Hypercholesterolemia was accompanied by extensive lipid accumulation in the liver and aorta, a characteristic feature of steatosis. The direct calcium assay demonstrated significantly increased mineralization of the muzzle skin containing the dermal sheath of vibrissae (57.2 ± 4.4 μmol Ca/gram tissue on the atherogenic diet and 43.9 ± 2.2 μmol Ca/gram tissue on control diet; P < 0.01), a reproducible biomarker of the ectopic mineralization process in these mice. An increased frequency of mineralization was also observed in the kidneys and eyes of mice on the atherogenic diet (P < 0.01).

Conclusion: These observations suggest that the atherogenic diet caused hypercholesterolemia and accelerated ectopic mineralization in the Abcc6 -/- mice. Our findings have clinical implications for patients with PXE, a currently intractable disorder with considerable morbidity and occasional mortality.

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