Cavendish Laboratory, University of Cambridge, Cambridge, United Kingdom.
Biophys J. 2013 Sep 3;105(5):1143-50. doi: 10.1016/j.bpj.2013.07.036.
A complete understanding of phagocytosis requires insight into both its biochemical and physical aspects. One of the ways to explore the physical mechanism of phagocytosis is to probe whether and how the target properties (e.g., size, shape, surface states, stiffness, etc.) affect their uptake. Here we report an imaging-based method to explore phagocytosis kinetics, which is compatible with real-time imaging and can be used to validate existing reports using fixed and stained cells. We measure single-event engulfment time from a large number of phagocytosis events to compare how size and shape of targets determine their engulfment. The data shows an increase in the average engulfment time for increased target size, for spherical particles. The uptake time data on nonspherical particles confirms that target shape plays a more dominant role than target size for phagocytosis: Ellipsoids with an eccentricity of 0.954 and much smaller surface areas than spheres were taken up five times more slowly than spherical targets.
要全面了解吞噬作用,需要深入了解其生化和物理方面。探索吞噬作用物理机制的一种方法是探究目标属性(例如大小、形状、表面状态、刚性等)是否以及如何影响它们的摄取。在这里,我们报告了一种基于成像的方法来探索吞噬作用动力学,该方法与实时成像兼容,可用于验证使用固定和染色细胞的现有报告。我们从大量吞噬作用事件中测量单次吞噬作用时间,以比较目标大小和形状如何决定它们的吞噬作用。数据显示,球形颗粒的目标尺寸增加,平均吞噬作用时间增加。非球形颗粒的摄取时间数据证实,对于吞噬作用,目标形状比目标尺寸起更主导作用:长半轴为 0.954 的椭圆体和比球体小得多的表面积的摄取速度比球形靶标慢五倍。