Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, CA 92121, USA.
Science. 2012 May 11;336(6082):717-21. doi: 10.1126/science.1215157. Epub 2012 Apr 5.
Osteoarthritis (OA) is a degenerative joint disease that involves the destruction of articular cartilage and eventually leads to disability. Molecules that promote the selective differentiation of multipotent mesenchymal stem cells (MSCs) into chondrocytes may stimulate the repair of damaged cartilage. Using an image-based high-throughput screen, we identified the small molecule kartogenin, which promotes chondrocyte differentiation (median effective concentration = 100 nM), shows chondroprotective effects in vitro, and is efficacious in two OA animal models. Kartogenin binds filamin A, disrupts its interaction with the transcription factor core-binding factor β subunit (CBFβ), and induces chondrogenesis by regulating the CBFβ-RUNX1 transcriptional program. This work provides new insights into the control of chondrogenesis that may ultimately lead to a stem cell-based therapy for osteoarthritis.
骨关节炎(OA)是一种退行性关节疾病,涉及关节软骨的破坏,最终导致残疾。促进多能间充质干细胞(MSCs)选择性分化为软骨细胞的分子可能会刺激受损软骨的修复。我们使用基于图像的高通量筛选方法,鉴定出了小分子卡托辛,它能促进软骨细胞分化(半数有效浓度=100nM),在体外具有软骨保护作用,并且在两种 OA 动物模型中有效。卡托辛与细丝蛋白 A 结合,破坏其与转录因子核心结合因子 β 亚基(CBFβ)的相互作用,并通过调节 CBFβ-RUNX1 转录程序诱导软骨生成。这项工作为控制软骨生成提供了新的见解,这可能最终导致基于干细胞的骨关节炎治疗方法。