Injectable Microgels with Hybrid Exosomes of Chondrocyte‐Targeted FGF18 Gene‐Editing and Self‐Renewable Lubrication for Osteoarthritis Therapy

Author:

Chen Manyu12,Lu Yan12,Liu Yuhan3,Liu Quanying4,Deng Siyan12,Liu Yuan5,Cui Xiaolin67,Liang Jie128,Zhang Xingdong12,Fan Yujiang12,Wang Qiguang12ORCID

Affiliation:

1. National Engineering Research Center for Biomaterials Sichuan University 29 Wangjiang Road Chengdu 610064 P. R. China

2. College of Biomedical Engineering Sichuan University 29 Wangjiang Road Chengdu 610064 P. R. China

3. The Third Affiliated Hospital of Jinzhou Medical University Jinzhou Liaoning 121000 P. R. China

4. Institute of Rocket Force Medicine State Key Laboratory of Trauma Burns and Combined Injury Third Military Medical University (Army Medical University) Chongqing 400038 P. R. China

5. Orthopedics Research Institute Department of Orthopedics West China Hospital Sichuan University Chengdu 610041 P. R. China

6. School of medicine the Chinese University of Hong Kong Shenzhen 518172 P. R. China

7. Department of Orthopedic Surgery & Musculoskeletal Medicine Centre for Bioengineering & Nanomedicine University of Otago Christchurch 8140 New Zealand

8. Sichuan Testing Center for Biomaterials and Medical Devices Sichuan University 29 Wangjiang Road Chengdu 610064 P. R. China

Abstract

AbstractAbnormal silencing of fibroblast growth factor (FGF) signaling significantly contributes to joint dysplasia and osteoarthritis (OA); However, the clinical translation of FGF18‐based protein drugs is hindered by their short half‐life, low delivery efficiency and the need for repeated articular injections. This study proposes a CRISPR/Cas9‐based approach to effectively activate the FGF18 gene of OA chondrocytes at the genome level in vivo, using chondrocyte‐affinity peptide (CAP) incorporated hybrid exosomes (CAP/FGF18‐hyEXO) loaded with an FGF18‐targeted gene‐editing tool. Furthermore, CAP/FGF18‐hyEXO are encapsulated in methacrylic anhydride‐modified hyaluronic (HAMA) hydrogel microspheres via microfluidics and photopolymerization to create an injectable microgel system (CAP/FGF18‐hyEXO@HMs) with self‐renewable hydration layers to provide persistent lubrication in response to frictional wear. Together, the injectable CAP/FGF18‐hyEXO@HMs, combined with in vivo FGF18 gene editing and continuous lubrication, have demonstrated their capacity to synergistically promote cartilage regeneration, decrease inflammation, and prevent ECM degradation both in vitro and in vivo, holding great potential for clinical translation.

Funder

National Natural Science Foundation of China

Higher Education Discipline Innovation Project

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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