Natural Morin-Based Metal Organic Framework Nanoenzymes Modulate Articular Cavity Microenvironment to Alleviate Osteoarthritis

Author:

Cai Jinhong12,Liu Lian-feng13,Qin Zainen12,Liu Shuhan12,Wang Yonglin14,Chen Zhengrong25,Yao Yi25,Zheng Li12,Zhao Jinmin124,Gao Ming12

Affiliation:

1. Collaborative Innovation Centre of Regenerative Medicine and Medical Bioresource Development and Application Co-constructed by the Province and Ministry, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.

2. Guangxi Engineering Center in Biomedical Materials for Tissue and Organ Regeneration, Guangxi Key Laboratory of Regenerative Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.

3. Department of Ultrasound, Guangxi Medical University Cancer Hospital, Nanning, 530021, China.

4. Department of Orthopedics, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.

5. Life Sciences Institute, Guangxi Medical University, Nanning, 530021, China.

Abstract

Osteoarthritis (OA) is always characterized as excessive reactive oxygen species (ROS) inside articular cavity. Mimicking natural metalloenzymes with metal ions as the active centers, stable metal organic framework (MOF) formed by natural polyphenols and metal ions shows great potential in alleviating inflammatory diseases. Herein, a series of novel copper-morin-based MOF (CuMHs) with different molar ratios of Cu 2+ and MH were employed to serve as ROS scavengers for OA therapy. As a result, CuMHs exhibited enhanced dispersion in aqueous solution, improved biocompatibility, and efficient ROS-scavenging ability compared to MH. On the basis of H 2 O 2 -stimulated chondrocytes, intracellular ROS levels were efficiently declined and cell death was prevented after treated by Cu 6 MH (Cu 2+ and MH molar ratio of 6:1). Meanwhile, Cu 6 MH also exhibited efficient antioxidant and anti-inflammation function by down-regulating the expression of IL6, MMP13, and MMP3, and up-regulating cartilage specific gene expression as well. Importantly, Cu 6 MH could repair mitochondrial function by increasing mitochondrial membrane potential, reducing the accumulation of calcium ions, as well as promoting ATP content production. In OA joint model, intra-articular (IA) injected Cu 6 MH suppressed the progression of OA. It endowed that Cu 6 MH might be promising nanoenzymes for the prevention and treatment of various inflammatory diseases.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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