Fondazione G. Monasterio CNR-Regione Toscana, Via Moruzzi n° 1, 56100, Pisa, Italy,
Mol Cell Biochem. 2013 Nov;383(1-2):223-30. doi: 10.1007/s11010-013-1770-z. Epub 2013 Aug 11.
The development of atherosclerosis is caused by the accumulation of lipid, inflammatory cytokine production, and the large amount of inflammatory cells in the arterial wall. It is now established that the presence of oxidized low-density lipoproteins (ox-LDL) has an important role in the pathogenesis of the disease. There are many scavenger receptors for ox-LDL, among which LOX-1 seems to be important for the induction of endothelial dysfunction and the other subsequent events that lead to the formation of atheromatous plaque. Our findings indicate the presence of a regulatory role induced by the presence of ox-LDL on LOX-1 through the amplification of IL-6 synthesis. This mechanism contributes to the upregulation of the ORL-1 gene expression in presence of risk factors. Many authors have shown the possibility to use LOX-1 as a good marker for the diagnosis and prognosis of coronary artery disease because it is easy to measure and more sensitive than other markers commonly used in the routine of laboratory medicine.
动脉粥样硬化的发展是由脂质的积累、炎性细胞因子的产生以及动脉壁中大量炎性细胞引起的。现在已经确定,氧化型低密度脂蛋白(ox-LDL)的存在在疾病的发病机制中具有重要作用。ox-LDL 有许多清道夫受体,其中 LOX-1 似乎对诱导内皮功能障碍和导致动脉粥样硬化斑块形成的其他后续事件很重要。我们的研究结果表明,ox-LDL 通过放大 IL-6 合成对 LOX-1 存在诱导的调节作用。这种机制有助于在存在危险因素的情况下上调 ORL-1 基因的表达。许多作者已经表明,LOX-1 可以作为诊断和预测冠状动脉疾病的良好标志物,因为它易于测量,并且比实验室医学常规中常用的其他标志物更敏感。