NIR-enhanced Pt single atom/g-C3N4 nanozymes as SOD/CAT mimics to rescue ATP energy crisis by regulating oxidative phosphorylation pathway for delaying osteoarthritis progression

Bibliographic Details
Title: NIR-enhanced Pt single atom/g-C3N4 nanozymes as SOD/CAT mimics to rescue ATP energy crisis by regulating oxidative phosphorylation pathway for delaying osteoarthritis progression
Authors: Jianhui Xiang, Xin Yang, Manli Tan, Jianfeng Guo, Yuting Ye, Jiejia Deng, Zhangrui Huang, Hanjie Wang, Wei Su, Jianwen Cheng, Li Zheng, Sijia Liu, Jingping Zhong, Jinmin Zhao
Source: Bioactive Materials, Vol 36, Iss , Pp 1-13 (2024)
Publisher Information: KeAi Communications Co., Ltd., 2024.
Publication Year: 2024
Collection: LCC:Materials of engineering and construction. Mechanics of materials
LCC:Biology (General)
Subject Terms: ATP energy crisis, Osteoarthritis progression, Oxidative phosphorylation pathway, Nanozymes, Materials of engineering and construction. Mechanics of materials, TA401-492, Biology (General), QH301-705.5
More Details: Osteoarthritis (OA) progresses due to the excessive generation of reactive oxygen and nitrogen species (ROS/RNS) and abnormal ATP energy metabolism related to the oxidative phosphorylation pathway in the mitochondria. Highly active single-atom nanozymes (SAzymes) can help regulate the redox balance and have shown their potential in the treatment of inflammatory diseases. In this study, we innovatively utilised ligand-mediated strategies to chelate Pt4+ with modified g-C3N4 by π–π interaction to prepare g–C3N4–loaded Pt single-atom (Pt SA/C3N4) nanozymes that serve as superoxide dismutase (SOD)/catalase (CAT) mimics to scavenge ROS/RNS and regulate mitochondrial ATP production, ultimately delaying the progression of OA. Pt SA/C3N4 exhibited a high loading of Pt single atoms (2.45 wt%), with an excellent photothermal conversion efficiency (54.71%), resulting in tunable catalytic activities under near-infrared light (NIR) irradiation. Interestingly, the Pt–N6 active centres in Pt SA/C3N4 formed electron capture sites for electron holes, in which g-C3N4 regulated the d-band centre of Pt, and the N-rich sites transferred electrons to Pt, leading to the enhanced adsorption of free radicals and thus higher SOD- and CAT-like activities compared with pure g-C3N4 and g–C3N4–loaded Pt nanoparticles (Pt NPs/C3N4). Based on the use of H2O2-induced chondrocytes to simulate ROS-injured cartilage in vitro and an OA joint model in vivo, the results showed that Pt SA/C3N4 could reduce oxidative stress-induced damage, protect mitochondrial function, inhibit inflammation progression, and rebuild the OA microenvironment, thereby delaying the progression of OA. In particular, under NIR light irradiation, Pt SA/C3N4 could help reverse the oxidative stress-induced joint cartilage damage, bringing it closer to the state of the normal cartilage. Mechanistically, Pt SA/C3N4 regulated the expression of mitochondrial respiratory chain complexes, mainly NDUFV2 of complex 1 and MT-ATP6 of ATP synthase, to reduce ROS/RNS and promote ATP production. This study provides novel insights into the design of artificial nanozymes for treating oxidative stress-induced inflammatory diseases.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2452-199X
Relation: http://www.sciencedirect.com/science/article/pii/S2452199X2400063X; https://doaj.org/toc/2452-199X
DOI: 10.1016/j.bioactmat.2024.02.018
Access URL: https://doaj.org/article/857dc020bda448f9b038c92956d508ce
Accession Number: edsdoj.857dc020bda448f9b038c92956d508ce
Database: Directory of Open Access Journals
More Details
ISSN:2452199X
DOI:10.1016/j.bioactmat.2024.02.018
Published in:Bioactive Materials
Language:English