Parkhurst M R, Saltzman W M
Department of Chemical Engineering, Johns Hopkins University, Baltimore, Maryland 21218.
Biophys J. 1992 Feb;61(2):306-15. doi: 10.1016/S0006-3495(92)81838-6.
Leukocytes must migrate through tissues to fulfill their role in the immune response, but direct methods for observing and quantifying cell motility have mostly been limited to migration on two-dimensional surfaces. We have now developed methods for examining neutrophil movement in a three-dimensional gel containing 0.1 to 0.7 mg/ml rat tail tendon collagen. Neutrophil-populated collagen gels were formed within flat glass capillary tubes, permitting direct observation with light microscopy. By following the tracks of individual cells over a 13.5-min observation period and comparing them to a stochastic model of cell movement, we quantified cell speed within a given gel by estimating a random motility coefficient (mu) and persistence time (P). The random motility coefficient changed significantly with collagen concentration in the gel, varying from 1.6 to 13.3 x 10(-9) cm2/s, with the maximum occurring at a collagen gel concentration of 0.3 mg/ml. The methods described may be useful for studying tissue dynamics and for evaluating the mechanism of cell movement in three-dimensional gels of extracellular matrix (ECM) molecules.
白细胞必须在组织中迁移以履行其在免疫反应中的作用,但观察和量化细胞运动的直接方法大多局限于在二维表面上的迁移。我们现已开发出在含有0.1至0.7mg/ml大鼠尾腱胶原蛋白的三维凝胶中检测中性粒细胞运动的方法。在扁平玻璃毛细管内形成充满中性粒细胞的胶原蛋白凝胶,以便用光镜直接观察。通过在13.5分钟的观察期内追踪单个细胞的轨迹,并将其与细胞运动的随机模型进行比较,我们通过估计随机运动系数(μ)和持续时间(P)来量化给定凝胶内的细胞速度。随机运动系数随凝胶中胶原蛋白浓度的变化而显著变化,范围从1.6至13.3×10^(-9) cm²/s,最大值出现在胶原蛋白凝胶浓度为0.3mg/ml时。所述方法可能有助于研究组织动力学以及评估细胞在细胞外基质(ECM)分子三维凝胶中的运动机制。