Extracellular Vesicles Functional “Brick‐Cement” Bio‐Integrated System for Annulus Fibrosus Repair

Author:

Shen Yifan1,Pang Libin2,Jiang Chao1,Jin Jiale1,Zhang Yijian3,Xing Hongyuan1,Li Jiafeng4,Wu Honghao1,Chen Jingyao5,Guan Ming1,Zhu Tonghe6,Gao Zhongyang1,Cui Wenguo2ORCID,Wang Yue1

Affiliation:

1. Spine lab, Department of Orthopedic Surgery The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou 310003 P. R. China

2. Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China

3. Department of Orthopedics The First Affiliated Hospital of Soochow University Soochow University Suzhou 215006 P. R. China

4. Department of Orthopedic Surgery The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou 310003 P. R. China

5. Core Facilities Zhejiang University School of Medicine Hangzhou 310058 P. R. China

6. School of Chemistry and Chemical Engineering Institute for Frontier Medical Technology Shanghai University of Engineering Science Shanghai 201620 P. R. China

Abstract

AbstractDue to the deficiency of mechanical supporting after discectomy and weak proliferative capacity of annulus fibrosus (AF) cells, the AF defect repair remains a clinical challenge. Herein, a myofibroblasts derived extracellular vesicles (M‐EVs) functional “brick‐cement” bio‐integrated system (M‐EVs@PGBgel) is developed to repair AF defect. The modified Poly(glycerol‐sebacate) (PGBS), “bio‐brick” layer, exhibited excellent support features on account of its elastomeric mechanical properties. The loaded M‐EVs in the “bio‐cement” layer activated ITGA6/PI3K/AKT pathway, regulated M2 macrophage polarization, thus synergistically promoting AF cell proliferation and migration. The “bio‐cement” layer integrated PGBS and remnant tissue at the defect through the Schiff base reaction and aided M‐EVs’ sustained release. This study demonstrated that M‐EVs@PGBgel significantly improved the disc's biological and mechanical properties in the AF defect microenvironments and promoted AF regeneration in vivo. The M‐EVs@PGBgel shows promise as an effective strategy to simultaneously address the mechanical imbalance and biological disruptions resulting from AF defect.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

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