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通过诱导 Nkx3.2 的出生后表达来抑制骨关节炎的进展。

Suppression of Osteoarthritis progression by post-natal Induction of Nkx3.2.

机构信息

Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.

Department of Medical Biotechnology, Dongguk University-Seoul, Seoul, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2021 Sep 24;571:188-194. doi: 10.1016/j.bbrc.2021.07.074. Epub 2021 Jul 27.

Abstract

Osteoarthritis (OA) is an incurable joint disease affecting 240 million elderly population, and major unmet medical needs exist for better therapeutic options for OA. During skeletal development, Nkx3.2 has been shown to promote chondrocyte differentiation and survival, but to suppress cartilage hypertrophy and blood vessel invasion. Here we show that Nkx3.2 plays a key role in osteoarthritis (OA) pathogenesis. Marked reduction of Nkx3.2 expression was observed in three different murine OA models. Consistent with these findings, analyses of surgery-induced and age-driven OA models revealed that cartilage-specific post-natal induction of Nkx3.2 can suppress OA progression in mice. These results suggest that Nkx3.2 may serve as a promising target for OA drug development.

摘要

骨关节炎(OA)是一种影响 2.4 亿老年人群体的无法治愈的关节疾病,对于更好的 OA 治疗方法存在着重大的未满足的医疗需求。在骨骼发育过程中,Nkx3.2 已被证明可促进软骨细胞的分化和存活,但可抑制软骨肥大和血管侵袭。在这里,我们表明 Nkx3.2 在骨关节炎(OA)发病机制中起关键作用。在三种不同的小鼠 OA 模型中均观察到 Nkx3.2 表达的明显减少。与这些发现一致,对手术诱导和年龄驱动的 OA 模型的分析表明,软骨特异性的 Nkx3.2 出生后诱导可抑制小鼠的 OA 进展。这些结果表明,Nkx3.2 可能成为 OA 药物开发的有希望的靶点。

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