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探测溶酶体膜通透性的方法。

Methods for Probing Lysosomal Membrane Permeabilization.

作者信息

Jäättelä Marja, Nylandsted Jesper

机构信息

Unit for Cell Death and Metabolism, Center for Autophagy, Recycling and Disease, Danish Cancer Society Research Center, Strandboulevarden 49, DK-2100 Copenhagen, Denmark.

出版信息

Cold Spring Harb Protoc. 2015 Nov 2;2015(11):975-8. doi: 10.1101/pdb.top070367.

Abstract

Cell death triggered by lysosomal membrane permeabilization (LMP) is gaining increased interest as target for cancer therapy, but the death pathway also plays an important role in normal physiology (e.g., during involution of the mammary gland). LMP-induced cell death is triggered by release of hydrolases including cysteine cathepsin proteases from the lysosomal lumen into the cytosol. Limited release of proteases to the cytoplasm induces apoptosis or apoptosis-like cell death, whereas massive LMP results in rapid cellular necrosis. Here we introduce three complementary methods for quantifying and visualizing LMP: (i) monitoring LMP by immunocytochemistry, (ii) visualizing LMP by fluorescent dextran release, and (iii) quantification of LMP by activity measurements of lysosomal enzymes in digitonin-extracted cytosol.

摘要

由溶酶体膜通透性(LMP)引发的细胞死亡作为癌症治疗靶点正日益受到关注,但其死亡途径在正常生理过程(如乳腺退化期间)中也起着重要作用。LMP诱导的细胞死亡是由包括半胱氨酸组织蛋白酶在内的水解酶从溶酶体腔释放到细胞质中引发的。蛋白酶向细胞质的有限释放会诱导细胞凋亡或凋亡样细胞死亡,而大量的LMP则会导致细胞迅速坏死。在这里,我们介绍三种用于量化和可视化LMP的互补方法:(i)通过免疫细胞化学监测LMP,(ii)通过荧光葡聚糖释放可视化LMP,以及(iii)通过对皂角苷提取的细胞质中溶酶体酶的活性测量来量化LMP。

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