Chondrocyte-specific genomic editing enabled by hybrid exosomes for osteoarthritis treatment
|Corresponding Author||Duan，Li; Xia，Jiang|
Rationale: A cell-specific delivery vehicle is required to achieve gene editing of the disease-associated cells, so the hereditable genome editing reactions are confined within these cells without affecting healthy cells. A hybrid exosome-based nano-sized delivery vehicle derived by fusion of engineered exosomes and liposomes will be able to encapsulate and deliver CRISPR/Cas9 plasmids selectively to chondrocytes embedded in articular cartilage and attenuate the condition of cartilage damage. Methods: Chondrocyte-targeting exosomes (CAP-Exo) were constructed by genetically fusing a chondrocyte affinity peptide (CAP) at the N-terminus of the exosomal surface protein Lamp2b. Membrane fusion of the CAP-Exo with liposomes formed hybrid CAP-exosomes (hybrid CAP-Exo) which were used to encapsulate CRISPR/Cas9 plasmids. By intra-articular (IA) administration, hybrid CAP-Exo/Cas9 sgMMP-13 entered the chondrocytes of rats with cartilage damages that mimicked the condition of osteoarthritis. Results: The hybrid CAP-Exo entered the deep region of the cartilage matrix in arthritic rats on IA administration, delivered the plasmid Cas9 sgMMP-13 to chondrocytes, knocked down the matrix metalloproteinase 13 (MMP-13), efficiently ablated the expression of MMP-13 in chondrocytes, and attenuated the hydrolytic degradation of the extracellular matrix proteins in the cartilage. Conclusion: Chondrocyte-specific knockdown of MMP-13 mitigates or prevents cartilage degradation in arthritic rats, showing that hybrid CAP-Exo/Cas9 sgMMP-13 may alleviate osteoarthritis.
National Key R&D Program of China[2018YFA0903204] ; University Grants Committee of Hong Kong["14307218","14304320","N_CUHK422/18","AoE/M-09/12"] ; RIF grant[R5013-19] ; CUHK-University of Manchester Joint Grant[RAC-2019/20] ; National Natural Science Foundation of China["81972116","81972085","81772394","31900046"] ; Guangdong International Cooperation Project[2021A0505030011] ; Guangdong Basic and Applied Basic Research Foundation["2020A1515011581","2021A1515010985"] ; Shenzhen Science and Technology Projects["JCYJ20200109150700942","JCYJ20180306170922163","SGDX20201103095800003","GJHZ20200731095606019"] ; China Postdoctoral Science Foundation["2020M682907","2021M702286"]
|WOS Research Area|
Research & Experimental Medicine
Medicine, Research & Experimental
|WOS Accession No|
Web of Science
Cited Times [WOS]:12
|Document Type||Journal Article|
|Department||Department of Biomedical Engineering|
1.Department of Orthopedics,the First Affiliated Hospital of Shenzhen University,Shenzhen Second People's Hospital,Shenzhen,518035,China
2.Department of Chemistry,the Chinese University of Hong Kong,Shatin,Hong Kong
3.Department of Biomedical Engineering,South University of Science and Technology of China,Shenzhen,518055,China
4.Department of Biomedical Engineering,The Hong Kong Polytechnic University,Hong Kong
5.Research Institute of Smart Ageing,The Hong Kong Polytechnic University,Hong Kong
Liang，Yujie,Xu，Xiao,Xu，Limei,et al. Chondrocyte-specific genomic editing enabled by hybrid exosomes for osteoarthritis treatment[J]. Theranostics,2022,12(11):4866-4878.
Liang，Yujie.,Xu，Xiao.,Xu，Limei.,Iqbal，Zoya.,Ouyang，Kan.,...&Xia，Jiang.(2022).Chondrocyte-specific genomic editing enabled by hybrid exosomes for osteoarthritis treatment.Theranostics,12(11),4866-4878.
Liang，Yujie,et al."Chondrocyte-specific genomic editing enabled by hybrid exosomes for osteoarthritis treatment".Theranostics 12.11(2022):4866-4878.
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