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Nano- to microscale dynamics of P-selectin detachment from leukocyte interfaces. I. Membrane separation from the cytoskeleton
被引:112
作者:
Evans, E
[1
]
Heinrich, V
Leung, A
Kinoshita, K
机构:
[1] Boston Univ, Boston, MA 02215 USA
[2] Univ British Columbia, Dept Pathol, Vancouver, BC V6T 2B5, Canada
[3] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V6T 2B5, Canada
关键词:
D O I:
10.1529/biophysj.104.051698
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
We have used a biomembrane force probe decorated with P-selectin to form point attachments with PSGL-1 receptors on a human neutrophil (PMN) in a calcium-containing medium and then to quantify the forces experienced by the attachment during retraction of the PMN at fixed speed. From first touch to final detachment, the typical force history exhibited the following sequence of events: i), an initial linear-elastic displacement of the PMN surface, ii), an abrupt crossover to viscoplastic flow that signaled membrane separation from the interior cytoskeleton and the beginning of a membrane tether, and iii), the final detachment from the probe tip by usually one precipitous step of P-selectin: PSGL-1 dissociation. In this first article I, we focus on the initial elastic response and its termination by membrane separation from the cytoskeleton, initiating tether formation. Quantifying membrane unbinding forces for rates of loading ( force/time) in the elastic regime from 240 pN/s to 38,000 pN/s, we discovered that the force distributions agreed well with the theory for kinetically limited failure of a weak bond. The kinetic rate for membrane unbinding was found to increase as an exponential function of the pulling force, characterized by an e-fold scale in force of; 17 pN and a preexponential factor, or apparent unstressed off rate, of similar to1/s. The rheological properties of tether growth subsequent to the membrane unbinding events are presented in a companion article II.
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页码:2288 / 2298
页数:11
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