| Literature DB >> 31602419 |
Stefanos Aivazidis1, Colin C Anderson1, James R Roede1.
Abstract
Disruption in redox signaling and control of cellular processes has emerged as a key player in many pathologies including neurodegeneration. As protein aggregations are a common hallmark of several neuronal pathologies, a firm understanding of the interplay between redox signaling, oxidative and free radical stress, and proteinopathies is required to sort out the complex mechanisms in these diseases. Fortunately, models of toxicant-induced neurodegeneration can be utilized to evaluate and report mechanistic alterations in the proteostasis network (PN). The epidemiological links between environmental toxicants and neurological disease gives further credence into characterizing the toxicant-mediated PN disruptions observed in these conditions. Reviewed here are examples of mechanistic interaction between oxidative or free radical stress and PN alterations. Additionally, investigations into toxicant-mediated PN disruptions, specifically focusing on environmental metals and pesticides, are discussed. Finally, we emphasize the need to distinguish whether the presence of protein aggregations are contributory to phenotypes related to neurodegeneration, or if they are a byproduct of PN deficiencies.Entities:
Keywords: Environmental Toxicants; Neurodegeneration; Oxidative Stress; Protein Aggregation; Proteostasis Network; Redox Proteome
Year: 2018 PMID: 31602419 PMCID: PMC6785977 DOI: 10.1016/j.cotox.2018.12.007
Source DB: PubMed Journal: Curr Opin Toxicol ISSN: 2468-2020