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受体介导的细胞附着与脱离动力学。II. 径向流脱离试验的实验模型研究。

Receptor-mediated cell attachment and detachment kinetics. II. Experimental model studies with the radial-flow detachment assay.

作者信息

Cozens-Roberts C, Quinn J A, Lauffenburger D A

机构信息

Department of Chemical Engineering, University of Pennsylvania, Philadelphia 19104.

出版信息

Biophys J. 1990 Oct;58(4):857-72. doi: 10.1016/S0006-3495(90)82431-0.

Abstract

Quantitative information regarding the kinetics of receptor-mediated cell adhesion to a ligand-coated surface are crucial for understanding the role of certain key parameters in many physiological and biotechnology-related processes. Here, we use the probabilistic attachment and detachment models developed in the preceding paper to interpret transient data from well-defined experiments. These data are obtained with a simple model cell system that consists of receptor-coated latex beads (prototype cells) and a Radial-Flow Detachment Assay (RFDA) using a ligand-coated glass disc. The receptors and ligands used in this work are complementary antibodies. The beads enable us to examine transient behavior with particles that possess fairly uniform properties that can be varied systematically, and the RFDA is designed for direct observation of adhesion to the ligand-coated glass surface over a range of shear stresses. Our experiments focus on the effects of surface shear stress, receptor density, and ligand density. These data provide a crucial test of the probabilistic framework. We show that these data can be explained with the probabilistic analyses, whereas they cannot be readily interpreted on the basis of a deterministic analysis. In addition, we examine transient data on cell adhesion reported from other assays, demonstrating the consistency of these data with the predictions of the probabilistic models.

摘要

关于受体介导的细胞与配体包被表面的黏附动力学的定量信息,对于理解某些关键参数在许多生理和生物技术相关过程中的作用至关重要。在此,我们使用前文所开发的概率性附着和脱离模型来解释明确实验中的瞬态数据。这些数据是通过一个简单的模型细胞系统获得的,该系统由受体包被的乳胶珠(原型细胞)和使用配体包被玻璃盘的径向流脱离测定法(RFDA)组成。本研究中使用的受体和配体是互补抗体。这些珠子使我们能够用具有相当均匀性质且可系统变化的颗粒来研究瞬态行为,并且RFDA设计用于在一系列剪切应力下直接观察对配体包被玻璃表面的黏附。我们的实验聚焦于表面剪切应力、受体密度和配体密度的影响。这些数据为概率框架提供了关键检验。我们表明这些数据能用概率分析来解释,而基于确定性分析则难以解释。此外,我们研究了其他测定法所报告的细胞黏附瞬态数据,证明这些数据与概率模型的预测一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4075/1281032/a3fa8548a02b/biophysj00122-0048-a.jpg

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