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Article ; Online: Chronic arsenic exposure suppresses proteasomal and autophagic protein degradation.

Augenstein, Isabell I / Nail, Alexandra N / Ferragut Cardoso, Ana P / States, J Christopher / Banerjee, Mayukh

Environmental toxicology and pharmacology

2024  Volume 107, Page(s) 104398

Abstract: Ubiquitin Proteasomal System (UPS) and autophagy dysregulation initiate cancer. These pathways are regulated by zinc finger proteins. Trivalent inorganic arsenic (iAs) displaces zinc from zinc finger proteins disrupting functions of important cellular ... ...

Abstract Ubiquitin Proteasomal System (UPS) and autophagy dysregulation initiate cancer. These pathways are regulated by zinc finger proteins. Trivalent inorganic arsenic (iAs) displaces zinc from zinc finger proteins disrupting functions of important cellular proteins. The effect of chronic environmental iAs exposure (100 nM) on UPS has not been studied. We tested the hypothesis that environmental iAs exposure suppresses UPS, activating autophagy as a compensatory mechanism. We exposed skin (HaCaT and Ker-CT; independent quadruplicates) and lung (BEAS-2B; independent triplicates) cell cultures to 0 or 100 nM iAs for 7 or 8 weeks. We quantified ER stress (XBP1 splicing employing Reverse Transcriptase -Polymerase Chain Reaction), proteasomal degradation (immunoblots), and initiation and completion of autophagy (immunoblots). We demonstrate that chronic iAs exposure suppresses UPS, initiates autophagy, but suppresses autophagic protein degradation in skin and lung cell lines. Our data suggest that chronic iAs exposure inhibits autophagy which subsequently suppresses UPS.
MeSH term(s) Arsenic/toxicity ; Proteolysis ; Arsenicals ; Proteasome Endopeptidase Complex ; Autophagy
Chemical Substances Arsenic (N712M78A8G) ; Arsenicals ; Proteasome Endopeptidase Complex (EC 3.4.25.1)
Language English
Publishing date 2024-02-23
Publishing country Netherlands
Document type Journal Article
ZDB-ID 1318302-3
ISSN 1872-7077 ; 1382-6689
ISSN (online) 1872-7077
ISSN 1382-6689
DOI 10.1016/j.etap.2024.104398
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