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体外侧视成像技术及人T白血病细胞在剪切流中与细胞间黏附分子-1黏附的分析

In vitro side-view imaging technique and analysis of human T-leukemic cell adhesion to ICAM-1 in shear flow.

作者信息

Cao J, Donell B, Deaver D R, Lawrence M B, Dong C

机构信息

Bioengineering Program, The Pennsylvania State University, University Park, Pennsylvania, 16802, USA.

出版信息

Microvasc Res. 1998 Mar;55(2):124-37. doi: 10.1006/mvre.1997.2064.

Abstract

The objective of the present study is to apply a novel side-view imaging technique to investigate T-leukemic Jurkat cell adhesion to a surface-immobilized ICAM-1 in shear flow, a ligand for leukocyte LFA-1. Images have revealed that Jurkat cell adhesion on ICAM-1 under flow conditions in vitro is quasistatic. The cell-substrate contact length steadily increased with time during the initial cell attachment to the ICAM-1-coated surface and subsequently decreased with time as the trailing edge of the cell membrane peeled away from the substrate under the influence of fluid shear forces. Changes in flow shear stresses, cell deformability, or substrate ligand strength resulted in a significant change in the characteristic adhesion binding time and contact length. A 3-D flow field with shear stresses acting on an adherent cell was calculated by using finite element methods based on cell shapes obtained from the in vitro images. The maximum shear stress acting on an actual cell body was found to be 3-5 times greater than the upstream inlet wall shear stress and was influenced by the extent of cell deformation within the flow channel. Therefore, the application of such a side-view imaging technique has provided a practical assay to study the mechanics of cell-surface adhesion in 3-D. The elongation of cells in shear flow tempers hydrodynamic shear forces on the cell, which affects the transients in cell-surface adhesion.

摘要

本研究的目的是应用一种新型侧视成像技术,以研究T淋巴细胞白血病Jurkat细胞在剪切流中与表面固定的细胞间黏附分子-1(ICAM-1,白细胞淋巴细胞功能相关抗原-1的配体)的黏附情况。图像显示,体外流动条件下Jurkat细胞在ICAM-1上的黏附是准静态的。在细胞最初附着于ICAM-1包被表面的过程中,细胞-底物接触长度随时间稳步增加,随后随着细胞膜后缘在流体剪切力作用下从底物上剥离,接触长度随时间减少。流动剪切应力、细胞变形能力或底物配体强度的变化导致特征性黏附结合时间和接触长度发生显著变化。基于从体外图像获得的细胞形状,使用有限元方法计算了作用于黏附细胞的具有剪切应力的三维流场。发现作用于实际细胞体的最大剪切应力比上游入口壁剪切应力大3至5倍,并且受流动通道内细胞变形程度的影响。因此,这种侧视成像技术的应用为研究三维细胞-表面黏附力学提供了一种实用的检测方法。剪切流中细胞的伸长缓和了作用于细胞的流体动力剪切力,这影响了细胞-表面黏附的瞬态过程。

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