Akiyama Haruhiko, Stadler H Scott, Martin James F, Ishii Takahiro M, Beachy Philip A, Nakamura Takashi, de Crombrugghe Benoit
Department of Orthopaedics, Kyoto University, Kyoto 606-8507, Japan.
Matrix Biol. 2007 May;26(4):224-33. doi: 10.1016/j.matbio.2006.12.002. Epub 2006 Dec 8.
Our previous studies have demonstrated the essential roles of the transcription factor Sox9 in the commitment of mesenchymal cells to a chondrogenic cell lineage and in overt chondrogenesis during limb bud development. However, it remains unknown if Sox9 induces chondrogenesis in mesenchyme ectopically in vivo as a master regulator of chondrogenesis. In this study, we first generated mutant mice in which Sox9 was misexpressed in the limb bud mesenchyme. The mutant mouse embryos exhibited polydactyly in limb buds in association with ectopic expression of Sox5 and Sox6 although markers for the different axes of limb bud development showed a normal pattern of expression. Misexpression of Sox9 stimulated cell proliferation in limb bud mesenchyme, suggesting that Sox9 has a role in recruiting mesenchymal cells to mesenchymal condensation. Second, despite the facts that misexpression of Sonic hedgehog (Shh) induces polydactyly in a number of mutant mice and Shh-null mutants have severely defective cartilage elements in limb buds, misexpression of Sox9 did not restore limb bud phenotypes in Shh-null mutants. Rather, there was no expression of Sox9 in digit I of Hoxa13Hd mutant embryos, and Sox9 partially rescued hypodactyly in Hoxa13Hd mutant embryos. These results provide evidence that Sox9 induces ectopic chondrogenesis in mesenchymal cells and strongly suggest that its expression may be regulated by Hox genes during limb bud development.
我们之前的研究已经证明,转录因子Sox9在间充质细胞向软骨细胞谱系的定向分化以及肢体芽发育过程中的明显软骨形成中起着至关重要的作用。然而,Sox9作为软骨形成的主要调节因子,在体内是否能异位诱导间充质细胞发生软骨形成仍不清楚。在本研究中,我们首先构建了Sox9在肢体芽间充质中错误表达的突变小鼠。突变小鼠胚胎的肢体芽出现多指畸形,伴有Sox5和Sox6的异位表达,尽管肢体芽发育不同轴的标志物显示出正常的表达模式。Sox9的错误表达刺激了肢体芽间充质中的细胞增殖,这表明Sox9在将间充质细胞募集到间充质凝聚中发挥作用。其次,尽管 Sonic hedgehog(Shh)的错误表达在许多突变小鼠中诱导多指畸形,并且Shh基因敲除突变体的肢体芽软骨元件存在严重缺陷,但Sox9的错误表达并未恢复Shh基因敲除突变体的肢体芽表型。相反,在Hoxa13Hd突变胚胎的第一指中没有Sox9的表达,并且Sox9部分挽救了Hoxa13Hd突变胚胎的少指畸形。这些结果提供了证据,表明Sox9可诱导间充质细胞发生异位软骨形成,并强烈表明其表达在肢体芽发育过程中可能受Hox基因调控。