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配体诱导多形核白细胞硬化的细胞转运分析

Cell transit analysis of ligand-induced stiffening of polymorphonuclear leukocytes.

作者信息

Nossal R

机构信息

Laboratory of Integrative and Medical Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Biophys J. 1998 Sep;75(3):1541-52. doi: 10.1016/S0006-3495(98)74073-1.

Abstract

A mathematical treatment of the mechanical behavior of transiently bonded polymer networks is used to interpret measurements of the pressure-induced passage of plant cells through microporous membranes. Cell transit times are inferred to be proportional to the instantaneous shear modulus of the cell cortex, a parameters that we then relate to properties of the cortical F-actin matrix. These theoretical results are used to analyze published data on chemoattractant-induced changes of rigidity of polymorphonuclear leukocytes. We thereby rationalize previously noted, peculiar, power-law logarithmic dependences of transit time on ligand concentration. As a consequence, we are able to deduce a linear relationship between the extent of F-actin polymerization and the logarithm of the chemoattractant concentration. The latter is examined with regard to the G-protein activation that is known to occur when chemoattractants bind to receptors on the surfaces of polymorphonuclear cells.

摘要

对瞬态键合聚合物网络的力学行为进行数学处理,以解释对植物细胞通过微孔膜的压力诱导通过的测量结果。推断细胞通过时间与细胞皮层的瞬时剪切模量成正比,我们随后将该参数与皮层F-肌动蛋白基质的特性联系起来。这些理论结果用于分析已发表的关于趋化因子诱导的多形核白细胞刚性变化的数据。由此,我们使先前注意到的通过时间对配体浓度的奇特幂律对数依赖性合理化。因此,我们能够推断出F-肌动蛋白聚合程度与趋化因子浓度对数之间的线性关系。后者针对已知在趋化因子与多形核细胞表面受体结合时发生的G蛋白激活进行了研究。

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本文引用的文献

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Small actin-binding proteins: the beta-thymosin family.小肌动蛋白结合蛋白:β-胸腺素家族
Curr Opin Cell Biol. 1993 Feb;5(1):56-62. doi: 10.1016/s0955-0674(05)80008-0.
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