Modeling of Biomechanics and Biorheology of Red Blood Cells in Type 2 Diabetes Mellitus

• Published in: Biophysical journal Vol. 113; no. 2; pp. 481 - 490
• Main Authors: Chang, Hung-Yu, Li, Xuejin, Karniadakis, George Em
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 25.07.2017; Biophysical Society; The Biophysical Society
• Subjects: Biomechanical Phenomena; Biomechanics; Blood flow; Cell Biophysics; Cell Membrane - physiology; Cell size; Computer applications; Computer Simulation; Deformability; Deformation; Diabetes; Diabetes mellitus; Diabetes Mellitus, Type 2 - blood; Diabetes Mellitus, Type 2 - pathology; Diabetes Mellitus, Type 2 - physiopathology; Elastic Modulus; Elasticity; Erythrocyte Deformability - physiology; Erythrocytes; Erythrocytes - pathology; Erythrocytes - physiology; Formability; Humans; Membranes; Microfluidics; Models, Cardiovascular; Patients; Rheological properties; Rheology; Shear flow; Simulation; Stiffening; Viscoelasticity; Viscosity
• ISSN: 0006-3495; 1542-0086; 1542-0086
• DOI: 10.1016/j.bpj.2017.06.015

Erythrocytes in patients with type-2 diabetes mellitus (T2DM) are associated with reduced cell deformability and elevated blood viscosity, which contribute to impaired blood flow and other pathophysiological aspects of diabetes-related vascular complications. In this study, by using a two-component red blood cell (RBC) model and systematic parameter variation, we perform detailed computational simulations to probe the alteration of the biomechanical, rheological, and dynamic behavior of T2DM RBCs in response to morphological change and membrane stiffening. First, we examine the elastic response of T2DM RBCs subject to static tensile forcing and their viscoelastic relaxation response upon release of the stretching force. Second, we investigate the membrane fluctuations of T2DM RBCs and explore the effect of cell shape on the fluctuation amplitudes. Third, we subject the T2DM RBCs to shear flow and probe the effects of cell shape and effective membrane viscosity on their tank-treading movement. In addition, we model the cell dynamic behavior in a microfluidic channel with constriction and quantify the biorheological properties of individual T2DM RBCs. Finally, we simulate T2DM RBC suspensions under shear and compare the predicted viscosity with experimental measurements. Taken together, these simulation results and their comparison with currently available experimental data are helpful in identifying a specific parametric model—the first of its kind, to our knowledge—that best describes the main hallmarks of T2DM RBCs, which can be used in future simulation studies of hematologic complications of T2DM patients.