Research Centre for Nanometer-Scale Science and Advanced Materials, NANOSAM, Faculty of Physics, Astronomy, and Applied Computer Science, Jagiellonian University, Reymonta 4, 30-059 Krakow, Poland.
Cardiovasc Diabetol. 2013 Jun 27;12:96. doi: 10.1186/1475-2840-12-96.
Glycemic memory of endothelial cells is an effect of long-lasting hyperglycemia and is a cause of various diabetics complications, that arises despite of the treatment targeted towards returning low glucose level in blood system. On the other hand, endothelial dysfunction, which is believed to be a main cause of cardiovascular complications, is exhibited in the changes of mechanical properties of cells. Although formation of the glycemic memory was widely investigated, its impact on the mechanical properties of endothelial cells has not been studied yet.
In this study, nanoindentaion with a tip of an atomic force microscope was used to probe the long-term changes (through 26 passages, c.a. 80 days) in mechanical properties of EA.hy926 endothelial cells cultured in hyperglycemic conditions. As a complementary method, alterations in the structure of actin cytoskeleton were visualized by fluorescent staining of F-actin.
We observed a gradual stiffening of the cells up to 20th passage for cells cultured in high glucose (25 mM). Fluorescence imaging has revealed that this behavior resulted from systematic remodeling of the actin cytoskeleton. In further passages, a drop in stiffness had occurred. The most interesting finding was recorded for cells transferred after 14 passages from high glucose to normal glucose conditions (5mM). After the transfer, the initial drop in stiffness was followed by a return of the cell stiffness to the value previously observed for cells cultured constantly in high glucose
Our results indicate that glycemic memory causes irreversible changes in stiffness of endothelial cells. The formation of the observed "stiffness memory" could be important in the context of vascular complications which develop despite the normalization of the glucose level.
内皮细胞的血糖记忆是长期高血糖的一种效应,是各种糖尿病并发症的原因之一,尽管治疗的目的是使血液系统中的葡萄糖水平恢复正常,但这些并发症仍然会出现。另一方面,内皮功能障碍被认为是心血管并发症的主要原因,其表现为细胞机械性能的变化。虽然血糖记忆的形成已经得到了广泛的研究,但它对内皮细胞机械性能的影响尚未得到研究。
在这项研究中,使用原子力显微镜的针尖进行纳米压痕,来探测在高糖条件下培养的 EA.hy926 内皮细胞的机械性能的长期变化(经过 26 个传代,约 80 天)。作为一种补充方法,通过对 F-肌动蛋白进行荧光染色来可视化肌动蛋白细胞骨架结构的变化。
我们观察到在高葡萄糖(25mM)培养的细胞中,细胞逐渐变硬,直到第 20 代。荧光成像显示,这种行为是由于肌动蛋白细胞骨架的系统重塑所致。在进一步的传代中,细胞硬度下降。最有趣的发现记录在从高葡萄糖转移到正常葡萄糖条件(5mM)的 14 代后培养的细胞中。转移后,细胞硬度最初下降,随后恢复到以前在高葡萄糖中培养的细胞所观察到的硬度值。
我们的结果表明,血糖记忆导致内皮细胞硬度的不可逆变化。所观察到的“硬度记忆”的形成可能在尽管葡萄糖水平正常化但仍发展的血管并发症的背景下很重要。