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人脐带间充质干细胞通过抑制疾病早期阶段NLRP3介导的滑膜炎症来抑制骨关节炎的进展。

Human Umbilical Cord Mesenchymal Stem Cells Inhibit the Progression of Osteoarthritis by Suppressing NLRP3-Mediated Synovial Inflammation in the Early Stages of the Disease.

作者信息

Li Yu, Ouyang Yu, Lang Ruibo, He Jing, Zheng Shuo, Ao Chunchun, Jiang Yijia, Xiao Huan, Li Mao, Li Changyong, Wu Dongcheng

机构信息

R&D Center, Wuhan Hamilton Biotechnology Co. Ltd, Wuhan, Hubei, China.

School of Public Health, Hubei University of Medicine, Shiyan, Hubei, China.

出版信息

Stem Cells Int. 2025 Aug 30;2025:7558817. doi: 10.1155/sci/7558817. eCollection 2025.

DOI:10.1155/sci/7558817
PMID:40919498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12413943/
Abstract

Osteoarthritis (OA) is the leading joint disease that causes joint pain and disability. Despite increasing progress regarding the therapeutic potential of human umbilical cord mesenchymal stem cells (UC-MSCs) for OA, effective strategies for the treatment of OA using UC-MSCs have not yet been developed in clinical practice. Our present study has proven that the early stage in OA rats is the main development stage of nod-like receptor heat protein domain protein 3 (NLRP3)-mediated synovial inflammation. The middle stage in OA rats is the main development stage of chondrocyte apoptosis. The late stage in OA rats is the main development stage of synovial fibrosis. The treatment of UC-MSCs in the early and middle stages of OA significantly reduced cartilage damage in rats, and improved the pathological structure of the knee joint. In comparison, UC-MSCs effectively reduced chondrocyte apoptosis in the early and middle stages of OA rats, but they only effectively reduced NLRP3-mediated synovial inflammation in the early stages of OA rats. Experiments in vitro showed that UC-MSCs could inhibit NLRP3-mediated pyroptosis of rat primary synovial cells (Rat-scs). In conclusion, our findings suggest that UC-MSCs exert therapeutic effects on OA, at least in part, through inhibiting NLRP3-mediated synovial inflammation in the early stage of OA.

摘要

骨关节炎(OA)是导致关节疼痛和残疾的主要关节疾病。尽管人类脐带间充质干细胞(UC-MSCs)治疗OA的潜在疗效取得了越来越多的进展,但在临床实践中尚未开发出使用UC-MSCs治疗OA的有效策略。我们目前的研究证明,OA大鼠的早期是核苷酸结合寡聚化结构域样受体热蛋白结构域相关蛋白3(NLRP3)介导的滑膜炎症的主要发展阶段。OA大鼠的中期是软骨细胞凋亡的主要发展阶段。OA大鼠的晚期是滑膜纤维化的主要发展阶段。在OA的早期和中期用UC-MSCs治疗可显著减少大鼠的软骨损伤,并改善膝关节的病理结构。相比之下,UC-MSCs在OA大鼠的早期和中期有效减少软骨细胞凋亡,但仅在OA大鼠的早期有效减少NLRP3介导的滑膜炎症。体外实验表明,UC-MSCs可抑制大鼠原代滑膜细胞(Rat-scs)的NLRP3介导的焦亡。总之,我们的研究结果表明,UC-MSCs至少部分地通过抑制OA早期NLRP3介导的滑膜炎症对OA发挥治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/9c1bcb329bdc/SCI2025-7558817.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/477d13f2918a/SCI2025-7558817.001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/e8756c60e6f5/SCI2025-7558817.003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/9c1bcb329bdc/SCI2025-7558817.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/477d13f2918a/SCI2025-7558817.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/ca5ed0371fa9/SCI2025-7558817.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/e8756c60e6f5/SCI2025-7558817.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/6056177c044f/SCI2025-7558817.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/ac1283d21a66/SCI2025-7558817.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a2d/12413943/9c1bcb329bdc/SCI2025-7558817.006.jpg

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本文引用的文献

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Stem Cell Res Ther. 2025 Mar 7;16(1):122. doi: 10.1186/s13287-025-04252-2.
2
Mesenchymal stem cells for chronic knee pain secondary to osteoarthritis: A systematic review and meta-analysis of randomized trials.间充质干细胞治疗骨关节炎所致慢性膝关节疼痛的随机对照试验的系统评价和荟萃分析。
Osteoarthritis Cartilage. 2024 Oct;32(10):1207-1219. doi: 10.1016/j.joca.2024.04.021. Epub 2024 May 20.
3
DDIT3/CHOP promotes LPS/ATP-induced pyroptosis in osteoblasts via mitophagy inhibition.
DDIT3/CHOP通过抑制线粒体自噬促进LPS/ATP诱导的成骨细胞焦亡。
Biochim Biophys Acta Mol Cell Res. 2024 Apr;1871(4):119712. doi: 10.1016/j.bbamcr.2024.119712. Epub 2024 Mar 22.
4
Inflammatory Fibroblast-Like Synoviocyte-Derived Exosomes Aggravate Osteoarthritis via Enhancing Macrophage Glycolysis.炎性成纤维样滑膜细胞衍生的外泌体通过增强巨噬细胞糖酵解加重骨关节炎。
Adv Sci (Weinh). 2024 Apr;11(14):e2307338. doi: 10.1002/advs.202307338. Epub 2024 Feb 11.
5
Na1.7 as a chondrocyte regulator and therapeutic target for osteoarthritis.作为软骨细胞调节剂和骨关节炎治疗靶点的 Na1.7。
Nature. 2024 Jan;625(7995):557-565. doi: 10.1038/s41586-023-06888-7. Epub 2024 Jan 3.
6
MiR-146b-5p enriched bioinspired exosomes derived from fucoidan-directed induction mesenchymal stem cells protect chondrocytes in osteoarthritis by targeting TRAF6.富马酸诱导间充质干细胞来源的 miR-146b-5p 富集仿生外泌体通过靶向 TRAF6 保护骨关节炎软骨细胞。
J Nanobiotechnology. 2023 Dec 18;21(1):486. doi: 10.1186/s12951-023-02264-9.
7
Engineering exosomes derived from subcutaneous fat MSCs specially promote cartilage repair as miR-199a-3p delivery vehicles in Osteoarthritis.工程化来源于皮下脂肪间充质干细胞的外泌体作为 miR-199a-3p 的递送载体专门促进骨关节炎中的软骨修复。
J Nanobiotechnology. 2023 Sep 22;21(1):341. doi: 10.1186/s12951-023-02086-9.
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J Nanobiotechnology. 2023 Sep 16;21(1):332. doi: 10.1186/s12951-023-02087-8.
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10
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Sci Adv. 2023 Jul 21;9(29):eadh4054. doi: 10.1126/sciadv.adh4054.