NEST, Istituto Nanoscienze-CNR and Scuola Normale Superiore, Piazza San Silvestro 12 , 56127 Pisa, Italy.
Sci Rep. 2013;3:1141. doi: 10.1038/srep01141. Epub 2013 Jan 25.
Lectin-like ox-LDL receptors (LOX-1) play a crucial role in the ox-LDL-induced pathological transformation of vessel-wall components, a crucial early step in atherogenesis. LOX-1 dynamics is quantitatively investigated in human endothelial cells (HUVECs) exposed to environmental nanotopographies. We demonstrate distinct nanotopography-induced cell phenotypes, characterized by different morphology, LOX-1 diffusivity and oligomerization state: HUVECs on flat surfaces exhibit the behavior found in pro-atherogenic conditions, while growth on nanogratings can interfere with LOX-1 dynamics and lead to a behavior characteristic of normal, non-pathological conditions.
凝集素样氧化型低密度脂蛋白受体(LOX-1)在氧化型低密度脂蛋白(ox-LDL)诱导的血管壁成分病理转化中发挥关键作用,这是动脉粥样硬化形成的关键早期步骤。本文定量研究了 LOX-1 在暴露于环境纳米形貌的人血管内皮细胞(HUVEC)中的动力学。我们证明了不同纳米形貌诱导的细胞表型,其特征在于不同的形态、LOX-1 扩散性和寡聚状态:在平面上的 HUVEC 表现出在促动脉粥样硬化条件下发现的行为,而在纳米光栅上的生长可以干扰 LOX-1 动力学,并导致正常、非病理条件下的特征行为。