Hoffmann Andrea, Czichos Stefan, Kaps Christian, Bächner Dietmar, Mayer Hubert, Kurkalli Basan Gowda, Zilberman Yoram, Turgeman Gadi, Pelled Gadi, Gross Gerhard, Gazit Dan
Osteo-Angiogenesis Group, Gesellschaft für Biotechnologische Forschung (GBF), Mascheroder Weg 1, 38124 Braunschweig, Germany.
J Cell Sci. 2002 Feb 15;115(Pt 4):769-81. doi: 10.1242/jcs.115.4.769.
The BMP2-dependent onset of osteo/chondrogenic differentiation in the acknowledged pluripotent murine mesenchymal stem cell line (C3H10T1/2) is accompanied by the immediate upregulation of Fibroblast Growth Factor Receptor 3 (FGFR3) and a delayed response by FGFR2. Forced expression of FGFR3 in C3H10T1/2 is sufficient for chondrogenic differentiation, indicating an important role for FGF-signaling during the manifestation of the chondrogenic lineage in this cell line. Screening for transcription factors exhibiting a chondrogenic capacity in C3H10T1/2 identified that the T-box containing transcription factor Brachyury is upregulated by FGFR3-mediated signaling. Forced expression of Brachyury in C3H10T1/2 was sufficient for differentiation into the chondrogenic lineage in vitro and in vivo after transplantation into muscle. A dominant-negative variant of Brachyury, consisting of its DNA-binding domain (T-box), interferes with BMP2-mediated cartilage formation. These studies indicate that BMP-initiated FGF-signaling induces a novel type of transcription factor for the onset of chondrogenesis in a mesenchymal stem cell line. A potential role for this T-box factor in skeletogenesis is further delineated from its expression profile in various skeletal elements such as intervertebral disks and the limb bud at late stages (18.5 d.p.c.) of murine embryonic development.
在公认的多能小鼠间充质干细胞系(C3H10T1/2)中,骨/软骨生成分化的BMP2依赖性起始伴随着成纤维细胞生长因子受体3(FGFR3)的立即上调以及FGFR2的延迟反应。在C3H10T1/2中强制表达FGFR3足以实现软骨生成分化,这表明FGF信号在该细胞系软骨生成谱系的表现过程中发挥重要作用。对在C3H10T1/2中表现出软骨生成能力的转录因子进行筛选,发现含T盒的转录因子Brachyury通过FGFR3介导的信号上调。在C3H10T1/2中强制表达Brachyury足以使其在体外分化为软骨生成谱系,并在移植到肌肉后在体内实现分化。由其DNA结合结构域(T盒)组成的Brachyury显性负变体干扰BMP2介导的软骨形成。这些研究表明,BMP启动的FGF信号诱导一种新型转录因子,以启动间充质干细胞系中的软骨生成。从该T盒因子在小鼠胚胎发育后期(18.5天胚龄)的各种骨骼元件(如椎间盘和肢芽)中的表达谱进一步描绘了其在骨骼发生中的潜在作用。