TY - JOUR
T1 - From Surface Protrusion to Tether Extraction
T2 - A Mechanistic Model
AU - Shao, Jin Yu
AU - Yu, Yan
AU - Oswald, Sara J.
N1 - Funding Information:
This work was supported by grants from NIH (R21HL108215) and AHA (10GRNT4020027).
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2017/11/13
Y1 - 2017/11/13
N2 - Human leukocyte rolling on the endothelium is essential for leukocyte emigration and it is a process regulated by many factors including shear stress, receptor-ligand kinetics, and mechanical properties of cells and molecules. During this process, both leukocytes and endothelial cells (ECs) are pulled by forces due to blood flow and both may experience surface protrusion and tether extraction. In this study, we established a two-scale (cellular and molecular) model of cellular deformation because of a point pulling force and illustrated how surface protrusion makes the transition to tether extraction, either gradually or abruptly. Our simulation results matched well with what was observed in the experiments conducted with the optical trap and the atomic force microscope. We found that, although the traditional method of determining the force loading rate and the protrusional stiffness were still reasonable, the crossover force should not be simply interpreted as the rupture force of the receptor-cytoskeleton linkage. With little modification, this model can be incorporated into any leukocyte rolling model as a module for more accurate and realistic simulation.
AB - Human leukocyte rolling on the endothelium is essential for leukocyte emigration and it is a process regulated by many factors including shear stress, receptor-ligand kinetics, and mechanical properties of cells and molecules. During this process, both leukocytes and endothelial cells (ECs) are pulled by forces due to blood flow and both may experience surface protrusion and tether extraction. In this study, we established a two-scale (cellular and molecular) model of cellular deformation because of a point pulling force and illustrated how surface protrusion makes the transition to tether extraction, either gradually or abruptly. Our simulation results matched well with what was observed in the experiments conducted with the optical trap and the atomic force microscope. We found that, although the traditional method of determining the force loading rate and the protrusional stiffness were still reasonable, the crossover force should not be simply interpreted as the rupture force of the receptor-cytoskeleton linkage. With little modification, this model can be incorporated into any leukocyte rolling model as a module for more accurate and realistic simulation.
KW - atomic force microscopy
KW - cell mechanics
KW - endothelial cells
KW - leukocyte rolling
KW - mathematical simulation
KW - optical trap
UR - http://www.scopus.com/inward/record.url?scp=85034106958&partnerID=8YFLogxK
U2 - 10.1021/acsbiomaterials.6b00553
DO - 10.1021/acsbiomaterials.6b00553
M3 - Article
AN - SCOPUS:85034106958
SN - 2373-9878
VL - 3
SP - 3036
EP - 3042
JO - ACS Biomaterials Science and Engineering
JF - ACS Biomaterials Science and Engineering
IS - 11
ER -