Ceria Nanoparticles as Copper Chaperones that Activate SOD1 for Synergistic Antioxidant Therapy to Treat Ischemic Vascular Diseases

© 2023 Wiley-VCH GmbH.

Détails bibliographiques
Publié dans:Advanced materials (Deerfield Beach, Fla.). - 1998. - 35(2023), 16 vom: 11. Apr., Seite e2208989
Auteur principal: Im, Gwang-Bum (Auteur)
Autres auteurs: Kim, Young Geon, Yoo, Tae Yong, Kim, Yeong Hwan, Kim, Kang, Hyun, Jiyu, Soh, Min, Hyeon, Taeghwan, Bhang, Suk Ho
Format: Article en ligne
Langue:English
Publié: 2023
Accès à la collection:Advanced materials (Deerfield Beach, Fla.)
Sujets:Journal Article anti-inflammation antioxidants nanozymes oxidative stress superoxide dismutase 1 Antioxidants Copper 789U1901C5 Superoxide Dismutase-1 plus... EC 1.15.1.1 Reactive Oxygen Species SOD1 protein, human
Description
Résumé:© 2023 Wiley-VCH GmbH.
All exogenous nanomaterials undergo rapid biotransformation once injected into the body and fall short of executing the intended purpose. Here, it is reported that copper-deposited ceria nanoparticles (CuCe NPs) exhibit enhanced antioxidant effects over pristine ceria nanoparticles, as the released copper buffers the depletion of glutathione while providing the bioavailable copper as a cofactor for the antioxidant enzyme, superoxide dismutase 1. The upregulated intracellular antioxidants along with the ceria nanoparticles synergistically scavenge reactive oxygen species and promote anti-inflammation and M2 polarization of macrophages by modulating signal transducer and activator of transcription 1 and 6 (STAT1 and STAT6). The therapeutic effect of CuCe NPs is demonstrated in ischemic vascular diseases (i.e., murine models of hindlimb ischemia and myocardial infarction) in which the copper-deposition affords increased perfusion and alleviation in tissue damage. The results provide rationale that metal oxide nanomaterials can be designed in a way to induce the upregulation of specific biological factors for optimal therapeutic performance
Description:Date Completed 21.04.2023
Date Revised 21.04.2023
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202208989