Targeting regulation of stem cell exosomes: Exploring novel strategies for aseptic loosening of joint prosthesis

Periprosthetic osteolysis is a major long-term complication of total joint replacement. A series of biological reactions caused by the interaction of wear particles at the prosthesis bone interface and surrounding bone tissue cells after artificial joint replacement are vital reasons for aseptic loo...

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Published inFrontiers in bioengineering and biotechnology Vol. 10; p. 925841
Main Authors Ma, Tian-Liang, Chen, Jing-Xian, Ke, Zhuo-Ran, Zhu, Peng, Hu, Yi-He, Xie, Jie
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 10.08.2022
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Summary:Periprosthetic osteolysis is a major long-term complication of total joint replacement. A series of biological reactions caused by the interaction of wear particles at the prosthesis bone interface and surrounding bone tissue cells after artificial joint replacement are vital reasons for aseptic loosening. Disorder of bone metabolism and aseptic inflammation induced by wear particles are involved in the occurrence and development of aseptic loosening of the prosthesis. Promoting osteogenesis and angiogenesis and mediating osteoclasts and inflammation may be beneficial in preventing the aseptic loosening of the prosthesis. Current research about the prevention and treatment of aseptic loosening of the prosthesis focuses on drug, gene, and stem cell therapy and has not yet achieved satisfactory clinical efficacy or has not been used in clinical practice. Exosomes are a kind of typical extracellular vehicle. In recent years, stem cell exosomes (Exos) have been widely used to regulate bone metabolism, block inflammation, and have broad application prospects in tissue repair and cell therapy.
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Edited by: Jun Li, University of Pennsylvania, United States
This article was submitted to Preclinical Cell and Gene Therapy, a section of the journal Frontiers in Bioengineering and Biotechnology
Reviewed by: Wonsae Lee, University of Pennsylvania, United States
These authors have contributed equally to this work
Ming-Hsien Chan, Academia Sinica, Taiwan
ISSN:2296-4185
2296-4185
DOI:10.3389/fbioe.2022.925841