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2020 年骨关节炎年度回顾:生物学。

Osteoarthritis year in review 2020: biology.

机构信息

Experimental Rheumatology, Radboud university medical center Nijmegen, the Netherlands..

出版信息

Osteoarthritis Cartilage. 2021 Feb;29(2):143-150. doi: 10.1016/j.joca.2020.10.006. Epub 2020 Nov 24.


DOI:10.1016/j.joca.2020.10.006
PMID:33242602
Abstract

This year in review about osteoarthritis biology highlights a selection of articles published between the 2019 and 2020 Osteoarthritis Research Society International (OARSI) World Congress meetings, within the field of osteoarthritis biology. Highlights were selected from PubMed searches covering osteoarthritis (OA) cartilage, subchondral bone, synovium and aging. Subsequently, a personal selection was based on new and emerging themes together with common research topics that were studied by multiple groups. Themes discussed include novel insights into the inflammatory changes during OA, with a number of noteworthy publications concerning the role of macrophages in healthy and osteoarthritic joints. Next, the application of mesenchymal stem cells as OA-dampening therapy is discussed, including possible ways to improve their efficacy by pre-treatment. Other significant themes including treatment of OA with metformin, enhancing autophagy to alleviate OA and the involvement of the gastro-intestinal microbiome in development of OA symptoms and structural damage are discussed. An effort was made to connect the seemingly distant topics from which the overarching conclusion can be drawn that over the last year promising breakthroughs have been achieved in further understanding the biology of OA development and that new therapeutic possibilities have been explored.

摘要

本年度关于骨关节炎生物学的回顾重点介绍了在骨关节炎研究协会国际(OARSI)2019 年和 2020 年世界大会会议之间发表的一系列骨关节炎生物学领域的文章。重点是从涵盖骨关节炎(OA)软骨、软骨下骨、滑膜和衰老的 PubMed 搜索中选择的。随后,根据新出现的主题和多个小组研究的常见研究主题进行了个人选择。讨论的主题包括 OA 期间炎症变化的新见解,有许多关于巨噬细胞在健康和骨关节炎关节中作用的有价值的出版物。接下来,讨论了间充质干细胞作为 OA 抑制治疗的应用,包括通过预处理提高其疗效的可能方法。其他重要主题包括二甲双胍治疗 OA、增强自噬以缓解 OA 以及胃肠道微生物组在 OA 症状和结构损伤发展中的参与,都进行了讨论。我们努力将看似遥远的主题联系起来,从中可以得出这样的结论:在过去的一年里,人们在进一步了解 OA 发展的生物学方面取得了有希望的突破,并探索了新的治疗可能性。

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Protective effect of cartilage oligomeric matrix protein (COMP) on osteoarthritis-like chondrocytes based on the nuclear factor kappa B (NF-κB) pathway.

J Mol Histol. 2025-8-8

[2]
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Front Cell Infect Microbiol. 2025-7-16

[3]
Wet-electrospun porous freeform scaffold enhances colonisation of cells.

Mater Today Bio. 2025-6-16

[4]
Isoginkgetin protects chondrocytes and inhibits osteoarthritis through NF-κB and P21 signaling pathway.

Mol Med. 2025-6-22

[5]
Unveiling the potential of MSC extracellular vesicles: MiR-122-5p enhancing chondrocyte regeneration in osteoarthritis via autophagy mechanism.

Stem Cell Res Ther. 2025-6-7

[6]
OA-HybridCNN (OHC): An advanced deep learning fusion model for enhanced diagnostic accuracy in knee osteoarthritis imaging.

PLoS One. 2025-5-7

[7]
Macrophages-derived small extracellular vesicles regulate chondrocyte proliferation and affect osteoarthritis progression via upregulating Osteopontin expression.

J Cell Commun Signal. 2025-4-22

[8]
Recent applications of stimulus-responsive smart hydrogels for osteoarthritis therapy.

Front Bioeng Biotechnol. 2025-2-17

[9]
Extracecellulr vesicles (EVs) microRNAs (miRNAs) derived from mesenchymal stem cells (MSCs) in osteoarthritis (OA); detailed role in pathogenesis and possible therapeutics.

Heliyon. 2025-1-27

[10]
Silk fibroin-based hydrogels for cartilage organoids in osteoarthritis treatment.

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