Ohta Yuji, Otsuka Chie, Okamoto Hiroshi
Faculty of Human Life and Environmental Sciences, Ochanomizu University, 2-1-1 Otsuka, Bunkyo-ku, Tokyo 112-8610, Japan.
J Artif Organs. 2003;6(2):101-5. doi: 10.1007/s10047-003-0217-9.
Blood cells are subject to various kinds of stresses in flow fields. Hemolysis is the phenomenon in which a higher stress than normal damages the erythrocyte membrane and results in the leakage of its contents. Even if the stress is not strong enough to cause cell lysis, however, the cell membrane may sustain some damage. Therefore, to further improve the blood compatibility of artificial organs, the mechanisms of sublethal damage must be investigated. As a first step, we have analyzed the fine surface structure of sheared erythrocytes from a microscopic viewpoint by using an atomic force microscope (AFM) featuring nano meter-scale visualization. Sheep erythrocytes were sheared by a conventional cylindrical viscometer under sublethal shearing conditions. The duration of shear was set at 10 s, and the shearing rate was set at 0 (as control), 10000, and 50000/s. After being stressed, the cell surfaces were visualized by an AFM and the surface roughness was measured. As a result, the roughness value was found to increase with the shearing rate: 4.5 +/- 1.5 nm (0/s, control), 6.9 +/- 2.1 nm (10000/s, P < 0.01), and 10.1 +/- 2.4 nm (50000/s, P < 0.01).
血细胞在流场中会受到各种应力作用。溶血是指比正常情况更高的应力破坏红细胞膜并导致其内容物泄漏的现象。然而,即使应力不够强以至于不会导致细胞裂解,细胞膜也可能会受到一些损伤。因此,为了进一步提高人造器官的血液相容性,必须研究亚致死损伤的机制。作为第一步,我们使用具有纳米级可视化功能的原子力显微镜(AFM)从微观角度分析了剪切红细胞的精细表面结构。在亚致死剪切条件下,用传统的圆柱形粘度计对绵羊红细胞进行剪切。剪切持续时间设定为10秒,剪切速率设定为0(作为对照)、10000和50000/秒。在施加应力后,用AFM观察细胞表面并测量表面粗糙度。结果发现,粗糙度值随剪切速率的增加而增大:4.5±1.5纳米(0/秒,对照)、6.9±2.1纳米(10000/秒,P<0.01)和10.1±2.4纳米(50000/秒,P<0.01)。