Ellegaard Anne-Marie, Jäättelä Marja, Nylandsted Jesper
Unit for Cell Death and Metabolism, Center for Autophagy, Recycling and Disease, Danish Cancer Society Research Center, DK-2100, Copenhagen, Denmark.
Cold Spring Harb Protoc. 2015 Oct 1;2015(10):900-3. doi: 10.1101/pdb.prot086173.
Lysosomal membrane permeabilization (LMP) is an effective programmed cell death pathway triggered in response to a variety of cytotoxic stimuli and cellular conditions. In the method presented here, LMP is monitored by first taking advantage of the steady endocytic capacity of cells to load fluorescent dextran into lysosomes, and then simply observing the translocation of lysosomally localized dextran into the cytosol after an LMP-inducing insult. Fluorescent dextran in healthy cells appears in punctate structures representing intact lysosomes, whereas after LMP, a diffuse staining pattern throughout the cytoplasm is observed. Using this method, LMP can be followed in real time using time-lapse imaging. The size of pores formed in the membrane during LMP by size exclusion can also be determined using dextrans of different sizes and colors.
溶酶体膜通透性(LMP)是一种有效的程序性细胞死亡途径,在多种细胞毒性刺激和细胞条件下被触发。在此介绍的方法中,监测LMP的过程如下:首先利用细胞稳定的内吞能力将荧光葡聚糖载入溶酶体,然后在LMP诱导性损伤后简单观察溶酶体定位的葡聚糖向细胞质的转运。健康细胞中的荧光葡聚糖呈点状结构,代表完整的溶酶体,而在LMP发生后,可观察到整个细胞质呈现弥漫性染色模式。使用该方法,可通过延时成像实时追踪LMP。通过使用不同大小和颜色的葡聚糖,还可以确定LMP过程中膜上形成的孔的大小。