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微环境在间充质干细胞治疗骨关节炎中的作用

Roles of Microenvironment on Mesenchymal Stem Cells Therapy for Osteoarthritis.

作者信息

Zhang Haiyan, Jin Chaoying, Hua Jiaqing, Chen Zuxiang, Gao Wenxin, Xu Wenting, Zhou Li, Shan Letian

机构信息

The Second Affiliated Hospital, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, People's Republic of China.

School of Medicine, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.

出版信息

J Inflamm Res. 2024 Oct 3;17:7069-7079. doi: 10.2147/JIR.S475617. eCollection 2024.

Abstract

Osteoarthritis (OA) induced microenvironmental alterations are a common and unavoidable phenomenon that greatly exacerbate the pathologic process of OA. Imbalances in the synthesis and degradation of cartilage extracellular matrix (ECM) have been reported to be associated with an adverse microenvironment. Stem cell therapy is a promising treatment for OA, and mesenchymal stem cells (MSCs) are the main cell sources for this therapy. With multispectral differentiation and immunomodulation, MSCs can effectively regulate the microenvironment of articular cartilage, ameliorate inflammation, promote regeneration of damaged cartilage, and ultimately alleviate OA symptoms. However, the efficacy of MSCs in the treatment of OA is greatly influenced by articular cavity microenvironments. This article reviews the five microenvironments of OA articular cavity, including inflammatory microenvironment, senescence microenvironment, hypoxic microenvironment, high glucose microenvironment and high lipid environment, focus on the positive and negative effects of OA microenvironments on the fate of MSCs. In this regard, we emphasize the mechanisms of the current use of MSCs in OA treatment, as well as its limitations and challenges.

摘要

骨关节炎(OA)引发的微环境改变是一种常见且不可避免的现象,会极大地加剧OA的病理进程。据报道,软骨细胞外基质(ECM)合成与降解的失衡与不良微环境有关。干细胞疗法是一种有前景的OA治疗方法,间充质干细胞(MSCs)是该疗法的主要细胞来源。通过多光谱分化和免疫调节,MSCs可有效调节关节软骨的微环境,减轻炎症,促进受损软骨再生,最终缓解OA症状。然而,MSCs治疗OA的疗效受关节腔微环境的影响很大。本文综述了OA关节腔的五种微环境,包括炎症微环境、衰老微环境、缺氧微环境、高糖微环境和高脂环境,重点探讨OA微环境对MSCs命运的正负影响。就此,我们强调了目前MSCs用于OA治疗的机制,以及其局限性和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8d6/11457791/eaf61f5c71c8/JIR-17-7069-g0001.jpg

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