Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Georgstraße 11, D-32545, Bad Oeynhausen, Germany.
University Eye Clinic Maastricht, Maastricht University Medical Center, 6202, AZ, Maastricht, The Netherlands.
Lipids Health Dis. 2019 Jan 5;18(1):2. doi: 10.1186/s12944-018-0943-x.
ATP-binding cassette (ABC) transporters are involved in a huge range of physiological processes. Mutations in the ABCC6 gene cause pseudoxanthoma elasticum, a metabolic disease with progressive soft tissue calcification.
The aim of the present study was to analyze gene expression levels of selected ABC transporters associated with cholesterol homeostasis in metabolic active tissues, such as the liver, kidney and white adipose tissue (WAT) of Abcc6 mice from an early and late disease stage (six-month-old and 12-month-old mice).
The strongest regulation of ABC transporter genes was observed in the liver tissue of six-month-old Abcc6 mice. Here, we found a significant increase of mRNA expression levels of phospholipid, bile salt and cholesterol/sterol transporters Abcb1b, Abcb11, Abcg1, Abcg5 and Abcg8. Abcd2 mRNA expression was increased by 3.2-fold in the liver tissue. We observed strong upregulation of Abca3 and Abca1 mRNA expression up to 3.3-fold in kidney and WAT, and a 2-fold increase of Abca9 mRNA in the WAT of six-month-old Abcc6 knockout mice. Gene expression levels of Abcb1b and Abcg1 remained increased in the liver tissue after an age-related disease progression, while we observed lower mRNA expression of Abca3 and Abca9 in the kidney and WAT of 12-month-old Abcc6 mice.
These data support previous findings that Abcc6 deficiency leads to an altered gene expression of other ABC transporters depending on the status of disease progression. The increased expression of fatty acid, bile salt and cholesterol/sterol transporters may be linked to an altered cholesterol and lipoprotein metabolism due to a loss of Abcc6 function.
ATP 结合盒(ABC)转运蛋白参与了广泛的生理过程。ABCC6 基因突变会导致假黄瘤弹性组织营养不良,这是一种具有进行性软组织钙化的代谢性疾病。
本研究旨在分析与胆固醇稳态相关的选定 ABC 转运蛋白的基因表达水平,这些转运蛋白存在于代谢活跃的组织中,如 Abcc6 小鼠的肝脏、肾脏和白色脂肪组织(WAT),这些 Abcc6 小鼠来自早期和晚期疾病阶段(6 月龄和 12 月龄小鼠)。
在 6 月龄 Abcc6 小鼠的肝组织中观察到 ABC 转运蛋白基因的最强调节。在这里,我们发现磷脂、胆汁盐和胆固醇/固醇转运蛋白 Abcb1b、Abcb11、Abcg1、Abcg5 和 Abcg8 的 mRNA 表达水平显著增加。Abcd2mRNA 在肝组织中的表达增加了 3.2 倍。我们观察到 Abca3 和 Abca1mRNA 在肾脏和 WAT 中的表达上调高达 3.3 倍,Abca9mRNA 在 6 月龄 Abcc6 敲除小鼠的 WAT 中增加了 2 倍。Abcb1b 和 Abcg1 的基因表达水平在与年龄相关的疾病进展后仍在肝组织中增加,而我们在 12 月龄 Abcc6 小鼠的肾脏和 WAT 中观察到 Abca3 和 Abca9mRNA 的表达降低。
这些数据支持先前的发现,即 Abcc6 缺乏会导致其他 ABC 转运蛋白的基因表达发生改变,这取决于疾病进展的状态。脂肪酸、胆汁盐和胆固醇/固醇转运蛋白的表达增加可能与 Abcc6 功能丧失导致的胆固醇和脂蛋白代谢改变有关。