Mularski Anna, Marie-Anaïs Florence, Mazzolini Julie, Niedergang Florence
Inserm, U1016, Institut Cochin, Paris, France.
CNRS, UMR 8104, Paris, France.
Methods Mol Biol. 2018;1784:165-175. doi: 10.1007/978-1-4939-7837-3_16.
Complementary methods to observe frustrated phagocytosis and phagosome closure using total internal reflection fluorescence microscopy (TIRFM) are described here. Frustrated phagocytosis occurs when phagocytic cells are exposed to an opsonized surface and spread as if trying to engulf it, allowing for the observation of phagocytic spreading and the biochemical events that directly precede it. Phagosome formation and closure is an inherently three-dimensional process though, and cannot be studied in the "frustrated" situation. Here we describe a method to visualize with unprecedented high-resolution phagosome formation and closure in three dimensions. It allows for observation of the base of the phagocytic cup, the extending pseudopods, as well as the precise site of phagosome scission.
本文介绍了使用全内反射荧光显微镜(TIRFM)观察受挫吞噬作用和吞噬体封闭的补充方法。当吞噬细胞暴露于调理素化表面并展开时,就会发生受挫吞噬作用,就好像试图吞噬它一样,从而可以观察到吞噬细胞的展开以及直接在此之前发生的生化事件。然而,吞噬体的形成和封闭是一个固有的三维过程,无法在“受挫”情况下进行研究。在这里,我们描述了一种以前所未有的高分辨率在三维空间中可视化吞噬体形成和封闭的方法。它可以观察吞噬杯的底部、延伸的伪足以及吞噬体分裂的确切位置。