Nandi Seema, Brown Ashley C
Joint Department of Biomedical Engineering, North Carolina State University and The University of North Carolina - Chapel Hill; Comparative Medicine Institute, North Carolina State University.
Joint Department of Biomedical Engineering, North Carolina State University and The University of North Carolina - Chapel Hill; Comparative Medicine Institute, North Carolina State University;
J Vis Exp. 2017 Aug 16(126):56099. doi: 10.3791/56099.
Currently, most in vitro models of wound healing, such as well-established scratch assays, involve studying cell migration and wound closure on two-dimensional surfaces. However, the physiological environment in which in vivo wound healing takes place is three-dimensional rather than two-dimensional. It is becoming increasingly clear that cell behavior differs greatly in two-dimensional vs. three-dimensional environments; therefore, there is a need for more physiologically relevant in vitro models for studying cell migration behaviors in wound closure. The method described herein allows for the study of cell migration in a three-dimensional model that better reflects physiological conditions than previously established two-dimensional scratch assays. The purpose of this model is to evaluate cell outgrowth via the examination of cell migration away from a spheroid body embedded within a fibrin matrix in the presence of pro- or anti-migratory factors. Using this method, cell outgrowth from the spheroid body in a three-dimensional matrix can be observed and is easily quantifiable over time via brightfield microscopy and analysis of spheroid body area. The effect of pro-migratory and/or inhibitory factors on cell migration can also be evaluated in this system. This method provides researchers with a simple method of analyzing cell migration in three-dimensional wound associated matrices in vitro, thus increasing the relevance of in vitro cell studies prior to the use of in vivo animal models.
目前,大多数伤口愈合的体外模型,如成熟的划痕试验,都涉及在二维表面上研究细胞迁移和伤口闭合。然而,体内伤口愈合发生的生理环境是三维的而非二维的。越来越明显的是,细胞在二维和三维环境中的行为有很大差异;因此,需要更具生理相关性的体外模型来研究伤口闭合中的细胞迁移行为。本文所述的方法允许在三维模型中研究细胞迁移,该模型比先前建立的二维划痕试验能更好地反映生理状况。该模型的目的是通过在存在促迁移或抗迁移因子的情况下,检查细胞从嵌入纤维蛋白基质中的球体迁移出去的情况,来评估细胞生长。使用这种方法,可以观察到三维基质中球体的细胞生长情况,并且通过明场显微镜和球体面积分析,随着时间的推移很容易进行量化。促迁移和/或抑制因子对细胞迁移的影响也可以在这个系统中进行评估。这种方法为研究人员提供了一种在体外三维伤口相关基质中分析细胞迁移的简单方法,从而在使用体内动物模型之前提高了体外细胞研究的相关性。