Virus-inspired lipopeptide-derived nucleic acid delivery to cartilage for osteoarthritis therapy

Cartilage-targeted gene therapy is promising for osteoarthritis (OA) treatment, though its potency critically depends on the effectiveness of delivery vectors. Here, we modularly develop a series of non-pathogenic, virus-inspired lipopeptide-based nanoparticles (VPN) tailored to deliver nucleic acids to cartilage. The cationic moiety of lipopeptide with variable arginine and histidine residues is the key functional component, and screened by in vitro performance. The optimized VPN-2 with a moiety of -[(R)<sub>5</sub>-(H)<sub>4</sub>]<sub>2</sub>- facilitates sufficient endocytosis and effective lysosomal escape, achieving about 2.5-fold improvement in transfection potency over conventional lipid nanoparticles. To address the tradeoff between penetration and retention within articular cartilage, si-VPN-2 is further formulated into ROS-responsive nano-in-gel system, which turns out to alleviate cartilage degeneration in surgical ACTL mice, and further synergizes with methylprednisolone to implement superior joint protection in PTOA mice. Our study underscores the platform's potential of VPN as cartilage-targeted RNA delivery vector for innovative OA therapy.

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Publication Details

Journal
Nature Communications
Published
2025-10-16
DOI
https://doi.org/10.1038/s41467-025-64212-5
Citations
2
Primary Topic
Osteoarthritis Treatment and Mechanisms
Type
article
Field-Weighted Citation Impact
3.34

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article

Virus-inspired lipopeptide-derived nucleic acid delivery to cartilage for osteoarthritis therapy

Zhenlan Fu, Yulan Huang, Zhigang Xu, L. Wang et al.
2 citations
Nature Communications
Osteoarthritis Treatment and Mechanisms
3.34
article

Virus-inspired lipopeptide-derived nucleic acid delivery to cartilage for osteoarthritis therapy

Zhenlan Fu, Yulan Huang, Zhigang Xu, L. Wang, Zhongyi Ma, Yu-Chun Wu, Jiayun Jiang, Yu Fu, Xing Zhou, Chong Li, Yunjiao Wang, Robert J. Lee, Jing Xie, Wenyun Cai, Yaqin Tang
article en
2 citations

Abstract

Cartilage-targeted gene therapy is promising for osteoarthritis (OA) treatment, though its potency critically depends on the effectiveness of delivery vectors. Here, we modularly develop a series of non-pathogenic, virus-inspired lipopeptide-based nanoparticles (VPN) tailored to deliver nucleic acids to cartilage. The cationic moiety of lipopeptide with variable arginine and histidine residues is the key functional component, and screened by in vitro performance. The optimized VPN-2 with a moiety of -[(R)<sub>5</sub>-(H)<sub>4</sub>]<sub>2</sub>- facilitates sufficient endocytosis and effective lysosomal escape, achieving about 2.5-fold improvement in transfection potency over conventional lipid nanoparticles. To address the tradeoff between penetration and retention within articular cartilage, si-VPN-2 is further formulated into ROS-responsive nano-in-gel system, which turns out to alleviate cartilage degeneration in surgical ACTL mice, and further synergizes with methylprednisolone to implement superior joint protection in PTOA mice. Our study underscores the platform's potential of VPN as cartilage-targeted RNA delivery vector for innovative OA therapy.

Nature CommunicationsVol. 16(1)
Southwest University (CN), Army Medical University (CN), Fudan University (CN), Southwest Hospital (CN), Chongqing Medical and Pharmaceutical College (CN), Chongqing University of Technology (CN), The Ohio State University (US), Southern Medical University (CN)
National Natural Science Foundation of China, Southwest University, State Key Laboratory of Molecular Engineering of Polymers, Centre Scientifique et Technique du Bâtiment, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 7%
Osteoarthritis Treatment and Mechanisms
3.34
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