Investigation on the effects of variable shear stress on monocyte cell morphology

Author(s):  
Semra Z. Birol ◽  
Rana Fucucuoglu ◽  
Sertac Cadirci ◽  
Ayca S. Yazgan ◽  
Levent Trabzon
2017 ◽  
Vol 12 (11) ◽  
pp. 881-885 ◽  
Author(s):  
Semra Zuhal Birol ◽  
Rana Fucucuoglu ◽  
Sertac Cadirci ◽  
Ayca Sayi‐Yazgan ◽  
Levent Trabzon

2019 ◽  
Vol 11 (10) ◽  
pp. 999-1003 ◽  
Author(s):  
Michael R Levitt ◽  
Christian Mandrycky ◽  
Ashley Abel ◽  
Cory M Kelly ◽  
Samuel Levy ◽  
...  

ObjectivesTo study the correlation between wall shear stress and endothelial cell expression in a patient-specific, three-dimensional (3D)-printed model of a cerebral aneurysm.Materials and methodsA 3D-printed model of a cerebral aneurysm was created from a patient’s angiogram. After populating the model with human endothelial cells, it was exposed to media under flow for 24 hours. Endothelial cell morphology was characterized in five regions of the 3D-printed model using confocal microscopy. Endothelial cells were then harvested from distinct regions of the 3D-printed model for mRNA collection and gene analysis via quantitative polymerase chain reaction (qPCR.) Cell morphology and mRNA measurement were correlated with computational fluid dynamics simulations.ResultsThe model was successfully populated with endothelial cells, which survived under flow for 24 hours. Endothelial morphology showed alignment with flow in the proximal and distal parent vessel and aneurysm neck, but disorganization in the aneurysm dome. Genetic analysis of endothelial mRNA expression in the aneurysm dome and distal parent vessel was compared with the proximal parent vessels. ADAMTS-1 and NOS3 were downregulated in the aneurysm dome, while GJA4 was upregulated in the distal parent vessel. Disorganized morphology and decreased ADAMTS-1 and NOS3 expression correlated with areas of substantially lower wall shear stress and wall shear stress gradient in computational fluid dynamics simulations.ConclusionsCreating 3D-printed models of patient-specific cerebral aneurysms populated with human endothelial cells is feasible. Analysis of these cells after exposure to flow demonstrates differences in both cell morphology and genetic expression, which correlate with areas of differential hemodynamic stress.


Author(s):  
В.Г. Кульков ◽  
А.А. Сыщиков

AbstractA model of internal friction at a grain boundary containing equidistant parallel cylindrical pores is presented. Variable shear stress induces a mutual displacement of the interfacial regions matched at the segments between pores depending on their position. The values of scattered energy at each segment and total internal friction are determined. The temperature dependence of the internal friction has a form of a wide peak.


Author(s):  
Leonie Rouleau ◽  
Monica Farcas ◽  
Jean-Claude Tardif ◽  
Rosaire Mongrain ◽  
Richard Leask

Endothelial cell (EC) dysfunction has been linked to atherosclerosis through their response to hemodynamic forces. Flow in stenotic vessels creates complex spatial gradients in wall shear stress. In vitro studies examining the effect of shear stress on endothelial cells have used unrealistic and simplified models, which cannot reproduce physiological conditions. The objective of this study was to expose endothelial cells to the complex shear shear pattern created by an asymmetric stenosis. Endothelial cells were grown and exposed for different times to physiological steady flow in straight dynamic controls and in idealized asymmetric stenosis models. Cells subjected to 1D flow aligned with flow direction and had a spindle-like shape when compared to static controls. Endothelial cell morphology was noticeable different in the regions with a spatial gradient in wall shear stress, being more randomly oriented and of cobblestone shape. This occurred despite the presence of an increased magnitude in shear stress. No other study to date has described this morphology in the presence of a positive wall shear stress gradient or gradient of significant shear magnitude. This technique provides a more realistic model to study endothelial cell response to spatial and temporal shear stress gradients that are present in vivo and is an important advancement towards a better understanding of the mechanisms involved in coronary artery disease.


2006 ◽  
Vol 34 (3) ◽  
pp. 436-445 ◽  
Author(s):  
Susan M. McCormick ◽  
Vikas Saini ◽  
Yigit Yazicioglu ◽  
Zoe N. Demou ◽  
Thomas J. Royston

PLoS ONE ◽  
2013 ◽  
Vol 8 (2) ◽  
pp. e57004 ◽  
Author(s):  
Joseph S. Uzarski ◽  
Edward W. Scott ◽  
Peter S. McFetridge

2017 ◽  
Vol 19 (4) ◽  
Author(s):  
David Barata ◽  
Giulia Spennati ◽  
Cristina Correia ◽  
Nelson Ribeiro ◽  
Björn Harink ◽  
...  

2017 ◽  
Vol 9 (4) ◽  
pp. 362-374 ◽  
Author(s):  
Jackson G. DeStefano ◽  
Ashley Williams ◽  
Alexa Wnorowski ◽  
Nahom Yimam ◽  
Peter C. Searson ◽  
...  

Real-time quantification of endothelial cell morphology and activity under applied shear stress.


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