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1.
J Artif Organs ; 24(2): 135-145, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33420875

ABSTRACT

Microparticles are produced by various cells due to a number of different stimuli in the circulatory system. Shear stress has been shown to injure red blood cells resulting in hemolysis or non-reversible sub-hemolytic damage. We hypothesized that, in the sub-hemolytic shear range, there exist sufficient mechanical stimuli for red blood cells to respond with production of microparticles. Red blood cells isolated from blood of healthy volunteers were exposed to high shear stress in a microfluidic channel to mimic mechanical trauma similar to that occurring in ventricular assist devices. Utilizing flow cytometry techniques, both an increase of shear rate and exposure time showed higher concentrations of red blood cell microparticles. Controlled shear rate exposure shows that red blood cell microparticle concentration may be indicative of sub-hemolytic damage to red blood cells. In addition, properties of these red blood cell microparticles produced by shear suggest that mechanical trauma may underlie some complications for cardiovascular patients.


Subject(s)
Cell-Derived Microparticles , Erythrocytes , Heart-Assist Devices/adverse effects , Stress, Mechanical , Hemolysis , Humans
2.
Sci Rep ; 9(1): 19443, 2019 12 19.
Article in English | MEDLINE | ID: mdl-31857631

ABSTRACT

Red blood cells (RBCs) passing through heart pumps, prosthetic heart valves and other cardiovascular devices undergo early senescence attributed to non-physiologic forces. We hypothesized that mechanical trauma accelerates aging by deformation of membrane proteins to cause binding of naturally occurring IgG. RBCs isolated from blood of healthy volunteers were exposed to high shear stress in a viscometer or microfluidics channel to mimic mechanical trauma and then incubated with autologous plasma. Increased binding of IgG was observed indicating forces caused conformational changes in a membrane protein exposing an epitope(s), probably the senescent cell antigen of band 3. The binding of immunoglobulin suggests it plays a role in the premature sequestration and phagocytosis of RBCs in the spleen. Measurement of IgG holds promise as a marker foreshadowing complications in cardiovascular patients and as a means to improve the design of medical devices in which RBCs are susceptible to sublethal trauma.


Subject(s)
Autoimmunity , Blood Viscosity , Erythrocytes/pathology , Heart Valve Prosthesis/adverse effects , Heart-Assist Devices/adverse effects , Autoantibodies/immunology , Autoantibodies/metabolism , Blood Circulation , Cardiovascular Diseases/surgery , Cardiovascular Surgical Procedures/adverse effects , Cardiovascular Surgical Procedures/instrumentation , Cell Membrane/immunology , Cell Membrane/metabolism , Epitopes/immunology , Epitopes/metabolism , Erythrocyte Aging/immunology , Erythrocytes/cytology , Erythrocytes/immunology , Humans , Immunoglobulin G/immunology , Immunoglobulin G/metabolism , Membrane Proteins/immunology , Membrane Proteins/metabolism , Prosthesis Design , Shear Strength , Stress, Mechanical
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