Jani Vivek P, Lucas Alfredo, Jani Vinay P, Munoz Carlos, Williams Alexander T, Ortiz Daniel, Yalcin Ozlem, Cabrales Pedro
School of Medicine, Johns Hopkins University, Baltimore, MD, United States.
Functional Cardiovascular Engineering, Department of Bioengineering, University of California, San Diego, San Diego, CA, United States.
Front Physiol. 2020 Jan 23;10:1562. doi: 10.3389/fphys.2019.01562. eCollection 2019.
The mechanical properties and deformability of Red Blood Cells (RBCs) are important determinants of blood rheology and microvascular hemodynamics. The objective of this study is to quantify the mechanical properties and wall shear stress experienced by the RBC membrane during capillary plug flow utilizing high speed video recording from intravital microscopy, biomechanical modeling, and computational methods. Capillaries were imaged in the rat cremaster muscle pre- and post-RBC transfusion of stored RBCs for 2-weeks. RBC membrane contours were extracted utilizing image processing and parametrized. RBC parameterizations were used to determine updated deformation gradient and Lagrangian Green strain tensors for each point along the parametrization and for each frame during plug flow. The updated Lagrangian Green strain and Displacement Gradient tensors were numerically fit to the Navier-Lame equations along the parameterized boundary to determined Lame's constants. Mechanical properties and wall shear stress were determined before and transfusion, were grouped in three populations of erythrocytes: native cells (NC) or circulating cells before transfusion, and two distinct population of cells after transfusion with stored cells (SC1 and SC2). The distinction, between the heterogeneous populations of cells present after the transfusion, SC1 and SC2, was obtained through principle component analysis (PCA) of the mechanical properties along the membrane. Cells with the first two principle components within 3 standard deviations of the mean, were labeled as SC1, and those with the first two principle components greater than 3 standard deviations from the mean were labeled as SC2. The calculated shear modulus average was 1.1±0.2, 0.90±0.15, and 12 ± 8 MPa for NC, SC1, and SC2, respectively. The calculated young's modulus average was 3.3±0.6, 2.6±0.4, and 32±20 MPa for NC, SC1, and SC2, respectively. o our knowledge, the methods presented here are the first estimation of the erythrocyte mechanical properties and shear stress during capillary plug flow. In summary, the methods introduced in this study may provide a new avenue of investigation of erythrocyte mechanics in the context of hematologic conditions that adversely affect erythrocyte mechanical properties.
红细胞(RBC)的力学性能和变形能力是血液流变学和微血管血液动力学的重要决定因素。本研究的目的是利用活体显微镜的高速视频记录、生物力学建模和计算方法,量化毛细血管栓流过程中红细胞膜所经历的力学性能和壁面剪应力。在大鼠提睾肌中,对储存2周的红细胞输血前后的毛细血管进行成像。利用图像处理提取红细胞膜轮廓并进行参数化。红细胞参数化用于确定栓塞流期间沿参数化的每个点以及每个帧的更新变形梯度和拉格朗日格林应变张量。更新后的拉格朗日格林应变和位移梯度张量沿参数化边界数值拟合到纳维-拉梅方程,以确定拉梅常数。在输血前后测定力学性能和壁面剪应力,将红细胞分为三个群体:天然细胞(NC)或输血前的循环细胞,以及输血后储存细胞的两个不同群体(SC1和SC2)。通过对沿膜的力学性能进行主成分分析(PCA),区分输血后出现的异质细胞群体SC1和SC2。前两个主成分在平均值的3个标准差范围内的细胞标记为SC1,前两个主成分大于平均值3个标准差的细胞标记为SC2。计算得出,NC、SC1和SC2的剪切模量平均值分别为1.1±0.2、0.90±0.15和12±8MPa。计算得出,NC、SC1和SC2的杨氏模量平均值分别为3.3±0.6、2.6±0.4和32±20MPa。据我们所知,这里介绍的方法是首次对毛细血管栓流过程中的红细胞力学性能和剪应力进行估计。总之,本研究中引入的方法可能为在不利影响红细胞力学性能的血液学条件下研究红细胞力学提供一条新途径。