Literature DB >> 31016653

Necrosome Formation and Necroptosis in Experimental Cholestasis.

Marta B Afonso1, Cecília M P Rodrigues2.   

Abstract

Necroptosis is emerging as a critical pathogenic mechanism in several liver diseases, including cholestatic disorders. Necroptosis was recently described as a novel cell death subroutine, activated downstream of death receptor stimulation and dependent on receptor-interacting serine/threonine-protein kinase 3 activity and mixed lineage kinase domain-like oligomerization and translocation to cell membrane. Here, we describe a combination of methods to evaluate necroptosis triggering in in vitro and in vivo models of cholestasis. Particularly, we detail alternative protocols to isolate total and soluble/insoluble protein extracts from tissues and cell cultures, as well as in vitro receptor-interacting serine/threonine-protein kinase 3 kinase activity assays, and subsequent Western blot analysis.

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Keywords:  Cell death; Cell signaling; Cholestasis; Insoluble protein fractions; Mixed lineage kinase domain-like (MLKL); Necroptosis; Necrosome; Receptor-interacting serine/threonine-protein kinase 3 (RIPK3); Tumor necrosis factor-α (TNF-α); Western blot

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Year:  2019        PMID: 31016653     DOI: 10.1007/978-1-4939-9420-5_10

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Vitexin ameliorates glycochenodeoxycholate-induced hepatocyte injury through SIRT6 and JAK2/STAT3 pathways.

Authors:  Chuang Zhang; Suolin Li; Chi Sun; Lin Liu; Yanbin Fang; Xiaofeng Yang; Xingxin Pan; Ben Zhang
Journal:  Iran J Basic Med Sci       Date:  2021-12       Impact factor: 2.699

  1 in total

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