Abstract

Osteoarthritis (OA) is a kind of degenerative disease, which is caused by many factors such as aging, obesity, strain, trauma, congenital joint abnormalities, joint deformities. Exosomes are mainly derived from the invagination of intracellular lysosomes, which are released into the extracellular matrix after fusion of the outer membrane of multi vesicles with the cell membrane. Exosomes mediate intercellular communication and regulate the biological activity of receptor cells by carrying non-coding RNA, long noncoding RNAs (lncRNAs), microRNAs (miRNAs), proteins and lipids. Evidences show that exosomes are involved in the pathogenesis of OA. In view of the important roles of exosomes in OA, this paper systematically reviewed the roles of exosomes in the pathogenesis of OA, including the roles of exosomes in OA diagnosis, the regulatory mechanisms of exosomes in the pathogenesis, and the intervention roles of exosomes in the treatment of OA. Reviewing the roles of exosomes in OA will help to clarify the pathogenesis of OA and explore new diagnostic biomarkers and therapeutic targets.

Highlights

  • Exosomes are small membrane bubbles (40–150 nm) containing complex RNAs and proteins

  • We reviewed the role of exosomes in the pathogenesis of OA, which will help to clarify the pathogenesis of OA and explore new diagnostic biomarkers and therapeutic targets

  • In exosomes derived from synovial fibroblasts, overexpressed miR-126-3p inhibits the chondrocyte inflammation and cartilage degradation in OA model rats, which may have certain therapeutic value for OA patients (Zhou et al, 2021)

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Summary

Introduction

Exosomes are small membrane bubbles (40–150 nm) containing complex RNAs and proteins. Synovial fluid derived exosomes recruit inflammatory cells, inhibit cartilage proliferation and promote joint degeneration. MiR-320c in the induced exosomes promotes the proliferation of OA chondrocytes and down-regulates the MMP13 expression more than that in control group.

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