右旋糖酐
内吞循环
细胞生物学
胞浆
细胞质
化学
荧光
细胞器
内吞作用
膜
溶酶体
生物物理学
染色
细胞
荧光染色
生物化学
生物
物理
遗传学
量子力学
酶
作者
Anne‐Marie Ellegaard,Marja Jäättelä,Jesper Nylandsted
出处
期刊:CSH Protocols
[Cold Spring Harbor Laboratory]
日期:2015-10-01
卷期号:2015 (10): pdb.prot086173-pdb.prot086173
被引量:15
标识
DOI:10.1101/pdb.prot086173
摘要
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.
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