Biomimetic Liposomes for G-Protein-Coupled Receptor 120 Exo/Endogenous Coactivation to Reprogram Lipid Metabolism in Obesity-Associated Osteoarthritis
Osteoarthritis (OA) associated with obesity is increasingly recognized as a distinct phenotype, driven by lipid metabolic imbalance and related inflammation. A particularly troublesome issue is that even after successfully correcting obesity, OA progression and lipid metabolic imbalance persist within the joint microenvironment, suggesting local lipid metabolism regulation as a potential treatment option. G-protein-coupled receptor 120 (GPR120), a primary receptor for long-chain fatty acids (including docosahexaenoic acid, DHA), has recently been found to play a pivotal role in regulating lipid homeostasis and suppressing inflammation. Here, we present ChD-FL/sgGPR, enabling dual endogenous-exogenous GPR120 activation. ChD-FL/sgGPR is a chondrocyte-biomimetic, fluorinated phenylboronic acid (FPBA)-modified ionizable liposome that codelivers DHA and a CRISPRa system comprising GPR120-specific sgRNA (single guide RNA) and dCas9-VPR mRNA (dead Cas9 fused to VP64-p65-Rta activator domain). Specifically, FPBA modification of liposomes enhances lysosomal escape and nuclear entry of RNA, while coextrusion with chondrocyte membranes facilitates cartilage-targeted delivery. In the coculture system of adipocytes and OA chondrocytes, ChD-FL/sgGPR significantly boosts chondrocytes GPR120 expression, facilitates lipid clearance via PPARγ signaling, and diminishes inflammatory mediators. In obese rat OA models, intra-articular injection of ChD-FL/sgGPR prolongs local retention, inhibits cartilage catabolism, and mitigates subchondral bone deterioration, collectively decelerating OA progression. By integrating CRISPR-mediated gene upregulation with DHA-induced receptor stimulation, this platform rebalances lipid metabolism in OA cartilage, offering a promising, mechanism-driven therapy for obesity-associated OA.
Authors
- Huiqi Xie (ORCID: https://orcid.org/0000-0003-0760-0853)
- Yi Zeng (ORCID: https://orcid.org/0000-0003-0473-2746)
- Changyang Gong (ORCID: https://orcid.org/0000-0002-2913-0891)
- Bin Shen (ORCID: https://orcid.org/0000-0002-9632-7221)
- Rui Wang (ORCID: https://orcid.org/0000-0003-4340-2977)
- Haibo Si (ORCID: https://orcid.org/0000-0002-4697-5597)
- Mingyang Li (ORCID: https://orcid.org/0000-0003-1766-7867)
- Hang Li (ORCID: https://orcid.org/0000-0002-6221-6195)
- Xiaoting Chen (ORCID: https://orcid.org/0000-0002-3782-3962)
- Yuangang Wu (ORCID: https://orcid.org/0000-0003-3516-4120)
- Jiehao Chen (ORCID: https://orcid.org/0009-0006-8843-0639)
- Mingjie Xu (ORCID: https://orcid.org/0000-0003-0419-7587)
- Limin Wu (ORCID: https://orcid.org/0009-0003-2803-0447)
- Qinjie Wu (ORCID: https://orcid.org/0000-0001-9229-9529)
- Meiling Shen
Institutions
- Sichuan University (CN)
- West China Hospital of Sichuan University (CN)
- China Animal Disease Control Center (CN)
- State Key Laboratory of Biotherapy
Publication Details
- Journal
- ACS Nano
- Published
- 2025-05-30
- DOI
- https://doi.org/10.1021/acsnano.5c02515
- Citations
- 5
- Primary Topic
- RNA Interference and Gene Delivery
- Type
- article
- Field-Weighted Citation Impact
- 4.03
Funders
- National Natural Science Foundation of China
- China Postdoctoral Science Foundation
- Department of Science and Technology of Sichuan Province
- Natural Science Foundation of Sichuan Province
- West China Hospital, Sichuan University