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使用新型光学设备TAXIScan对嗜酸性粒细胞趋化性进行定量分析。

Quantitative analysis of eosinophil chemotaxis tracked using a novel optical device -- TAXIScan.

作者信息

Nitta Nao, Tsuchiya Tomoko, Yamauchi Akira, Tamatani Takuya, Kanegasaki Shiro

机构信息

Central Lab, Effector Cell Institute, Inc., 4-7-7, Aobadai, Meguro-ku, Tokyo 153-0042, Japan.

出版信息

J Immunol Methods. 2007 Mar 30;320(1-2):155-63. doi: 10.1016/j.jim.2006.12.010. Epub 2007 Jan 22.

DOI:10.1016/j.jim.2006.12.010
PMID:17289072
Abstract

We have reported previously the development of an optically accessible, horizontal chemotaxis apparatus, in which migration of cells in the channel from a start line can be traced with time-lapse intervals using a CCD camera (JIM 282, 1-11, 2003). To obtain statistical data of migrating cells, we have developed quantitative methods to calculate various parameters in the process of chemotaxis, employing human eosinophil and CXCL12 as a model cell and a model chemoattractant, respectively. Median values of velocity and directionality of each cell within an experimental period could be calculated from the migratory pathway data obtained from time-lapse images and the data were expressed as Velocity-Directionality (VD) plot. This plot is useful for quantitatively analyzing multiple migrating cells exposed to a certain chemoattractant, and can distinguish chemotaxis from random migration. Moreover precise observation of cell migration revealed that each cell had a different lag period before starting chemotaxis, indicating variation in cell sensitivity to the chemoattractant. Thus lag time of each cell before migration, and time course of increment of the migrating cell ratio at the early stages could be calculated. We also graphed decrement of still moving cell ratio at the later stages by calculating the duration time of cell migration of each cell. These graphs could distinguish different motion patterns of chemotaxis of eosinophils, in response to a range of chemoattractants; PGD(2), fMLP, CCL3, CCL5 and CXCL12. Finally, we compared parameters of eosinophils from normal volunteers, allergy patients and asthma patients and found significant difference in response to PGD(2). The quantitative methods described here could be applicable to image data obtained with any combination of cells and chemoattractants and useful not only for basic studies of chemotaxis but also for diagnosis and for drug screening.

摘要

我们之前报道过一种光学可及的水平趋化性装置,在该装置中,通道内细胞从起始线开始的迁移可以使用电荷耦合器件(CCD)相机以时间间隔进行追踪(《日本免疫学会杂志》282卷,1 - 11页,2003年)。为了获得迁移细胞的统计数据,我们开发了定量方法来计算趋化过程中的各种参数,分别使用人类嗜酸性粒细胞和CXCL12作为模型细胞和模型趋化因子。实验期间每个细胞的速度和方向性的中位数可以根据从延时图像获得的迁移路径数据计算得出,这些数据以速度 - 方向性(VD)图表示。该图对于定量分析暴露于特定趋化因子的多个迁移细胞很有用,并且可以区分趋化性和随机迁移。此外,对细胞迁移的精确观察表明,每个细胞在开始趋化之前都有不同的延迟期,这表明细胞对趋化因子的敏感性存在差异。因此,可以计算每个细胞迁移前的延迟时间以及早期迁移细胞比例增加的时间进程。我们还通过计算每个细胞的迁移持续时间来绘制后期仍在移动的细胞比例的下降图。这些图可以区分嗜酸性粒细胞对一系列趋化因子(前列腺素D2、甲酰甲硫氨酸 - 亮氨酸 - 苯丙氨酸、CCL3、CCL5和CXCL12)的不同趋化运动模式。最后,我们比较了正常志愿者、过敏患者和哮喘患者的嗜酸性粒细胞参数,发现它们对前列腺素D2的反应存在显著差异。这里描述的定量方法可适用于通过细胞和趋化因子的任何组合获得的图像数据,不仅对趋化性的基础研究有用,而且对诊断和药物筛选也有用。

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