tether extraction
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2016 ◽  
Vol 3 (11) ◽  
pp. 3036-3042 ◽  
Author(s):  
Jin-Yu Shao ◽  
Yan Yu ◽  
Sara J. Oswald

Author(s):  
Jin-Yu Shao ◽  
Baoyu Liu

During leukocyte rolling on the endothelium, membrane tethers can be extracted simultaneously from both leukocytes and endothelial cells because of the force imposed by the blood flow [1]. Tether extraction has been shown to stabilize leukocyte rolling by increasing the lifetime of the adhesive selectin-ligand bonds that mediate leukocyte rolling [2]. Over the past two decades, tether extraction has been studied extensively, both experimentally and theoretically. In contrast, much less is known about tether retraction.


2011 ◽  
Vol 101 (1) ◽  
pp. 43-52 ◽  
Author(s):  
B. Pontes ◽  
N.B. Viana ◽  
L.T. Salgado ◽  
M. Farina ◽  
V. Moura Neto ◽  
...  

2010 ◽  
Vol 38 (12) ◽  
pp. 3756-3765 ◽  
Author(s):  
Yong Chen ◽  
Da-Kang Yao ◽  
Jin-Yu Shao

2008 ◽  
Vol 295 (5) ◽  
pp. C1434-C1444 ◽  
Author(s):  
Gang Xu ◽  
Jin-Yu Shao

Mechanical properties of neutrophils have been recognized as key contributors to stabilizing neutrophil rolling on the endothelium during the inflammatory response. In particular, accumulating evidence suggests that surface protrusion and tether extraction from neutrophils facilitate stable rolling by relieving the disruptive forces on adhesive bonds. Using a customized optical trap setup, we applied piconewton-level pulling forces on targeted receptors that were located either on the microvillus tip (CD162) or intermicrovillus surface of neutrophils (CD18 and CD44). Under a constant force-loading rate, there always occurred an initial tent-like surface protrusion that was terminated either by rupture of the adhesion or by a “yield” or “crossover” to tether extraction. The corresponding protrusional stiffness of neutrophils was found to be between 0.06 and 0.11 pN/nm, depending on the force-loading rate and the cytoskeletal integrity, but not on the force location, the medium osmolality, nor the temperature increase from 22°C to 37°C. More importantly, we found that neutrophil surface protrusion was accompanied by force relaxation and hysteresis. In addition, the crossover force did not change much in the range of force-loading rates studied, and the protrusional stiffness of lymphocytes was similar to that of neutrophils. These results show that neutrophil surface protrusion is essentially viscoelastic, with a protrusional stiffness that stems primarily from the actin cortex, and the crossover force is independent of the receptor-cytoskeleton interaction.


2007 ◽  
Vol 292 (4) ◽  
pp. C1272-C1279 ◽  
Author(s):  
Yong Chen ◽  
Gaurav Girdhar ◽  
Jin-Yu Shao

Membrane tethers were found to be extracted from leukocytes and macrovascular endothelial cells (e.g., human umbilical vein endothelial cells or HUVECs) when a point pulling force was exerted. These tethers stabilize leukocyte rolling on the endothelium during the inflammatory response. However, little is known about tether extraction from other vascular cells like microvascular endothelial cells (MECs). In this study, we extracted tethers from both adult and neonatal dermal MECs with the micropipette aspiration technique. We found a linear relationship between the pulling force and tether growth velocity for both cell lines. This constitutive relationship is mainly determined by the membrane mechanical property and the underlying actin-based cytoskeleton for both attached and suspended endothelial cells. It is independent of cell surface receptor type, attachment state, cytokine stimulation, or cell lineage. For both types of MECs, the threshold forces are ∼50 pN and the effective viscosities are around 0.5 pN·s/μm. These results, which are close to what was obtained from HUVECs, indicate that homogeneity is preserved in terms of tether extraction among different types of endothelial cells, and simultaneous tethers are likely extracted when leukocytes roll on either microvascular or macrovascular surfaces.


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