GAPDH inhibition mediated by thiol oxidation in human airway epithelial cells exposed to an environmental peroxide.
In: Redox biology, Jg. 73 (2024-07-01), S. 103199
Online
academicJournal
Zugriff:
Intracellular redox homeostasis in the airway epithelium is closely regulated through adaptive signaling and metabolic pathways. However, inhalational exposure to xenobiotic stressors such as secondary organic aerosols (SOA) can alter intracellular redox homeostasis. Isoprene hydroxy hydroperoxide (ISOPOOH), a ubiquitous volatile organic compound derived from the atmospheric photooxidation of biogenic isoprene, is a major contributor to SOA. We have previously demonstrated that exposure of human airway epithelial cells (HAEC) to ISOPOOH induces oxidative stress through multiple mechanisms including lipid peroxidation, glutathione oxidation, and alterations of glycolytic metabolism. Using dimedone-based reagents and copper catalyzed azo-alkynyl cycloaddition to tag intracellular protein thiol oxidation, we demonstrate that exposure of HAEC to micromolar levels of ISOPOOH induces reversible oxidation of cysteinyl thiols in multiple intracellular proteins, including GAPDH, that was accompanied by a dose-dependent loss of GAPDH enzymatic activity. These results demonstrate that ISOPOOH induces an oxidative modification of intracellular proteins that results in loss of GAPDH activity, which ultimately impacts the dynamic regulation of the intracellular redox homeostatic landscape in HAEC.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2024. Published by Elsevier B.V.)
Titel: |
GAPDH inhibition mediated by thiol oxidation in human airway epithelial cells exposed to an environmental peroxide.
|
---|---|
Autor/in / Beteiligte Person: | Masood, S ; Kim, HH ; Pennington, ER ; Tallman, KA ; Porter, NA ; Bromberg, PA ; Rice, RL ; Gold, A ; Zhang, Z ; Samet, JM |
Link: | |
Zeitschrift: | Redox biology, Jg. 73 (2024-07-01), S. 103199 |
Veröffentlichung: | [Amsterdam]: Elsevier, B.V., [2013]-, 2024 |
Medientyp: | academicJournal |
ISSN: | 2213-2317 (electronic) |
DOI: | 10.1016/j.redox.2024.103199 |
Schlagwort: |
|
Sonstiges: |
|