Department of Ocean and Mechanical Engineering, Florida Atlantic University.
Department of Ocean and Mechanical Engineering, Florida Atlantic University; Center for SMART Health, Florida Atlantic University;
J Vis Exp. 2023 Oct 13(200). doi: 10.3791/65897.
Red blood cells (RBCs) are known for their remarkable deformability. They repeatedly undergo considerable deformation when passing through the microcirculation. Reduced deformability is seen in physiologically aged RBCs. Existing techniques to measure cell deformability cannot easily be used for measuring fatigue, the gradual degradation in cell membranes caused by cyclic loads. We present a protocol to evaluate mechanical degradation in RBCs from cyclic shear stresses using amplitude shift keying (ASK) modulation-based electrodeformation in a microfluidic channel. Briefly, the interdigitated electrodes in the microfluidic channel are excited with a low voltage alternating current at radio frequencies using a signal generator. RBCs in suspension respond to the electric field and exhibit positive dielectrophoresis (DEP), which moves cells to the electrode edges. Cells are then stretched due to the electrical forces exerted on the two cell halves, resulting in uniaxial stretching, known as electrodeformation. The level of shear stress and the resultant deformation can be easily adjusted by changing the amplitude of the excitation wave. This enables quantifications of nonlinear deformability of RBCs in response to small and large deformations at high throughput. Modifying the excitation wave with the ASK strategy induces cyclic electrodeformation with programmable loading rates and frequencies. This provides a convenient way for the characterization of RBC fatigue. Our ASK-modulated electrodeformation approach enables, for the first time, a direct measurement of RBC fatigue from cyclic loads. It can be used as a tool for general biomechanical testing, for analyses of cell deformability and fatigue in other cell types and diseased conditions, and can also be combined with strategies to control the microenvironment of cells, such as oxygen tension and biological and chemical cues.
红细胞(RBCs)以其出色的变形能力而闻名。它们在通过微循环时会反复经历相当大的变形。生理老化的 RBC 的变形能力会降低。现有的测量细胞变形能力的技术不容易用于测量疲劳,即细胞膜由于循环载荷而逐渐降解。我们提出了一种使用基于幅度键控(ASK)调制的微流控通道中的电极变形来评估 RBC 从循环剪切应力引起的机械降解的方案。简而言之,微流控通道中的叉指电极使用信号发生器在射频上用低电压交流电激励。悬浮中的 RBC 对电场做出反应并表现出正介电泳(DEP),将细胞移动到电极边缘。然后,由于作用在两个细胞半部分上的电力,细胞被拉伸,导致细胞发生单轴拉伸,即电极变形。通过改变激励波的幅度,可以轻松调整剪切应力水平和产生的变形。这使得能够以高通量对 RBC 对小和大变形的非线性变形能力进行定量。通过 ASK 策略修改激励波可以诱导具有可编程加载速率和频率的循环电极变形。这为 RBC 疲劳的表征提供了一种便捷的方法。我们的 ASK 调制电极变形方法首次能够直接测量来自循环载荷的 RBC 疲劳。它可以用作通用生物力学测试的工具,用于分析其他细胞类型和疾病条件下的细胞变形能力和疲劳,并且还可以与控制细胞微环境的策略结合使用,例如氧张力和生物和化学线索。