Runx1缓解衰老小鼠骨关节炎的进展。

Pub Date : 2024-06-01 Epub Date: 2023-11-15 DOI:10.1080/01478885.2023.2281790
Haoran Chen, Caixia Pi, Mingyang Chen, Xinmei Du, Yujia Cui, Demao Zhang, Qiang Guo, Jing Xie, Xuedong Zhou
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引用次数: 0

摘要

随着年龄的增长,骨关节炎(OA)的发病率迅速增长,是老年人慢性残疾的最常见原因。与骨关节炎相关的不适和运动减少对生活质量有重大影响,并且没有已知的解决方案。runt相关转录因子1(Runx1)已被证明通过促进软骨形成在骨关节炎的发展中发挥保护作用。采用前交叉韧带横断法(ACLT)建立了老龄骨关节炎小鼠模型,并分析了关节内注射腺相关病毒/Runx1 (AAV/Runx1)对模型的影响。结果显示,注射AAV- runx1后,AAV/ runx1组比OA组保持了更好的关节软骨完整性,保留了更多的蛋白多糖。与软骨病理变化相关的标志物下调,而与软骨生理变化相关的标志物上调。这表明Runx1可能会阻碍衰老小鼠膝关节的OA进展,可能在OA中发挥保护作用,并可能成为未来老年患者骨关节炎的治疗靶点。
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Runx1 alleviates osteoarthritis progression in aging mice.

With rates growing quickly with age, osteoarthritis (OA) is the most common cause of chronic disability in aging persons. The discomfort and reduced motion associated with osteoarthritis have a significant impact on quality of life, and there is no known solution. Runt-related transcription factor 1(Runx1) has been shown to play a protective role in the development of osteoarthritis by promoting chondrogenesis. We had created models of ageing mice with osteoarthritis by anterior cruciate ligament transection (ACLT) and analyzed the effects of intra-articular injection of adeno-associated virus/Runx1 (AAV/Runx1) on the models. The results showed that the AAV/Runx1-group maintained better articular cartilage integrity and retained more proteoglycan than the OA group after injection of AAV-Runx1. The markers related to pathological changes in cartilage were downregulated, while the markers related to physiological changes in cartilage were upregulated. This suggests that Runx1 may impede OA progression on the knee joint of ageing mice, potentially playing a protective role in OA and becoming a probable treatment target for osteoarthritis among ageing patients in the future.

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