Role of glucose in the repair of cell membrane damage during squeeze distortion of erythrocytes in microfluidic capillaries.

The rapid development of portable precision detection methods and the crisis of insufficient blood supply worldwide has led scientists to study mechanical visualization features beyond the biochemical properties of erythrocytes. Combined evaluation of currently known biochemical biomarkers and mechanical morphological biomarkers will become the mainstream of single-cell detection in the future. To explore the mechanical morphology of erythrocytes, a microfluidic capillary system was constructed in vitro, with flow velocity and glucose concentration as the main variables, and the morphology and ability of erythrocytes to recover from deformation as the main objects of analysis. We showed the mechanical distortion of erythrocytes under various experimental conditions. Our results showed that glucose plays important roles in improving the ability of erythrocytes to recover from deformation and in repairing the damage caused to the cell membrane during the repeated squeeze process. These protective effects were also confirmed in in vivo experiments. Our results provide visual detection markers for single-cell chips and may be useful for future studies in cell aging.

[1]  Yu Sun,et al.  Stiffness and ATP recovery of stored red blood cells in serum , 2019, Microsystems & Nanoengineering.

[2]  N. M. Geekiyanage,et al.  A coarse-grained red blood cell membrane model to study stomatocyte-discocyte-echinocyte morphologies , 2019, PloS one.

[3]  Yi Zhang,et al.  Ultrafast water harvesting and transport in hierarchical microchannels , 2018, Nature Materials.

[4]  P. Schultz,et al.  A metabolite-derived protein modification integrates glycolysis with KEAP1-NRF2 signaling , 2018, Nature.

[5]  D. Yoon,et al.  A highly permselective electrochemical glucose sensor using red blood cell membrane. , 2018, Biosensors & bioelectronics.

[6]  Shuhong Liu,et al.  Lactic Dehydrogenase in the In Vitro Evaluation of Hemolytic Properties of Ventricular Assist Device , 2017, Artificial organs.

[7]  Lin Sun,et al.  Red cell distribution width as a significant indicator of medication and prognosis in type 2 diabetic patients , 2017, Scientific Reports.

[8]  E. Pretorius,et al.  The stabilizing effect of an oligomeric proanthocyanidin on red blood cell membrane structure of poorly controlled Type II diabetes , 2017, Nutrition & diabetes.

[9]  I. Melnik,et al.  Mechanism of changing adaptation potential and morpho-biochemical parameters of erythrocytes in students with different modes of daily activity after physical loading , 2017 .

[10]  B. Palsson,et al.  Biomarkers defining the metabolic age of red blood cells during cold storage. , 2016, Blood.

[11]  E. Pretorius,et al.  Erythrocytes and their role as health indicator: Using structure in a patient-orientated precision medicine approach. , 2016, Blood reviews.

[12]  Deyuan Zhang,et al.  Continuous directional water transport on the peristome surface of Nepenthes alata , 2016, Nature.

[13]  G. Lippi,et al.  Red blood cell distribution width and cardiovascular disorders. Does it really matter which comes first, the chicken or the egg? , 2016, International journal of cardiology.

[14]  H. Zimmermann,et al.  Study of SEM preparation artefacts with correlative microscopy: Cell shrinkage of adherent cells by HMDS-drying. , 2016, Scanning.

[15]  Antonio Cassinese,et al.  Microconfined flow behavior of red blood cells. , 2016, Medical engineering & physics.

[16]  J. Zimring Established and theoretical factors to consider in assessing the red cell storage lesion. , 2015, Blood.

[17]  Bernie Hansen,et al.  Red blood cell storage lesion. , 2015, Journal of veterinary emergency and critical care.

[18]  M. Gladwin,et al.  Towards microfluidic-based depletion of stiff and fragile human red cells that accumulate during blood storage. , 2014, Lab on a chip.

[19]  L. Zolla,et al.  Label-free quantitation of phosphopeptide changes in erythrocyte membranes: towards molecular mechanisms underlying deformability alterations in stored red blood cells , 2014, Haematologica.

[20]  Fumihito Arai,et al.  Red blood cell fatigue evaluation based on the close-encountering point between extensibility and recoverability. , 2014, Lab on a chip.

[21]  L. D. Da Costa,et al.  Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders. , 2013, Blood reviews.

[22]  Alison M. Forsyth,et al.  Red blood cell dynamics: from cell deformation to ATP release. , 2011, Integrative biology : quantitative biosciences from nano to macro.

[23]  Gabriel Popescu,et al.  Measurement of red blood cell mechanics during morphological changes , 2010, Proceedings of the National Academy of Sciences.

[24]  C. Lindsell,et al.  Evidence for Interindividual Heterogeneity in the Glucose Gradient Across the Human Red Blood Cell Membrane and Its Relationship to Hemoglobin Glycation , 2008, Diabetes.

[25]  Sergey S Shevkoplyas,et al.  Direct measurement of the impact of impaired erythrocyte deformability on microvascular network perfusion in a microfluidic device. , 2006, Lab on a chip.

[26]  E. Friedman,et al.  Association of reduced red blood cell deformability and diabetic nephropathy. , 2005, Kidney international.

[27]  N. White,et al.  Abnormal blood flow and red blood cell deformability in severe malaria. , 2000, Parasitology today.

[28]  G. Whitesides,et al.  Fabrication of microfluidic systems in poly(dimethylsiloxane) , 2000, Electrophoresis.

[29]  A. Pries,et al.  Biophysical aspects of blood flow in the microvasculature. , 1996, Cardiovascular research.

[30]  T. Secomb,et al.  Analysis of red blood cell motion through cylindrical micropores: effects of cell properties. , 1996, Biophysical journal.

[31]  R. Skalak,et al.  Flow of axisymmetric red blood cells in narrow capillaries , 1986, Journal of Fluid Mechanics.