Lin Francis
Laboratory of Immunology and Vascular Biology, Department of Pathology, School of Medicine, Stanford University, Stanford, California, USA.
Methods Enzymol. 2009;461:333-47. doi: 10.1016/S0076-6879(09)05415-9.
Leukocyte trafficking in tissues mediates cellular immune responses and can be directed by chemotactic factors such as chemokines. Understanding chemotactic responses of leukocytes to chemoattractant gradients is of great interest and importance to both basic science and clinical research. Conventional methods for studying leukocyte migration and chemotaxis generally lack the ability to maintain and manipulate gradient profiles. In contrast, microfluidic devices can generate well-defined stable chemical gradients and can precisely modify gradient conditions in space and time. Previously, microfluidic gradient-generating devices have been used to investigate various aspects of leukocyte migration in different chemoattractant fields with the focus on human blood neutrophils. Recently, chemotaxis of human blood T cells in chemokine gradients was successfully demonstrated in a microfluidic device. In this chapter, the detailed method of analyzing the migration of human blood neutrophils and T cells in chemoattractant gradients with microfluidic devices is described.
白细胞在组织中的迁移介导细胞免疫反应,并可由趋化因子(如趋化因子)引导。了解白细胞对趋化因子梯度的趋化反应对基础科学和临床研究都具有极大的兴趣和重要性。研究白细胞迁移和趋化性的传统方法通常缺乏维持和操纵梯度分布的能力。相比之下,微流控装置可以产生定义明确的稳定化学梯度,并能在空间和时间上精确改变梯度条件。此前,微流控梯度生成装置已被用于研究白细胞在不同趋化因子场中迁移的各个方面,重点是人类血液中的中性粒细胞。最近,在微流控装置中成功证明了人类血液T细胞在趋化因子梯度中的趋化性。在本章中,描述了使用微流控装置分析人类血液中性粒细胞和T细胞在趋化因子梯度中迁移的详细方法。