| Literature DB >> 31016653 |
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.Entities:
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