Jin Eun-Jung, Park Kwang Sook, Bang Ok-Sun, Kang Shin-Sung
Department of Biology, College of Natural Sciences (BK21), Kyungpook National University, Daegu 702-701, Korea.
J Cell Biochem. 2007 Sep 1;102(1):252-61. doi: 10.1002/jcb.21430.
Endochondral ossification is initiated by the differentiation of mesenchymal precursor cells to chondrocytes. This process is characterized by a strong interdependence of cell shape and cytoskeletal organization accompanying the onset of chondrogenic gene expression, but the molecular mechanisms mediating these interactions are not known. In this study, we hypothesized that the activation of matrix metalloproteinase (MMP)-2 would be involved in the reorganization of the actin cytoskeleton and that this would require an Akt-dependent signaling pathway in chick wing bud mesenchymal cells. The pharmacological inhibition of Akt signaling resulted in decreased glycosaminoglycan synthesis and reduced the level of active MMP-2, leading to suppressed cortical actin organization which is characteristic of differentiated chondrocytes. In addition, the exposure of cells to bafilomycin A1 reversed these chondro-inhibitory effects induced by inhibition of Akt signaling. In conclusion, our data indicate that Akt signaling is involved in the activation of MMP-2 and that this Akt-induced activation of MMP-2 is responsible for reorganization of the actin cytoskeleton into a cortical pattern with parallel rounding of chondrogenic competent cells.
软骨内骨化是由间充质前体细胞向软骨细胞的分化启动的。这一过程的特点是,伴随着软骨生成基因表达的开始,细胞形状与细胞骨架组织之间存在强烈的相互依存关系,但介导这些相互作用的分子机制尚不清楚。在本研究中,我们假设基质金属蛋白酶(MMP)-2的激活会参与肌动蛋白细胞骨架的重组,并且这在鸡翼芽间充质细胞中需要一条Akt依赖的信号通路。对Akt信号的药理学抑制导致糖胺聚糖合成减少,并降低了活性MMP-2的水平,从而导致分化软骨细胞特有的皮质肌动蛋白组织受到抑制。此外,将细胞暴露于巴弗洛霉素A1可逆转由Akt信号抑制诱导的这些软骨抑制作用。总之,我们的数据表明,Akt信号参与了MMP-2的激活,并且这种由Akt诱导的MMP-2激活负责将肌动蛋白细胞骨架重组为具有平行变圆的软骨生成能力细胞的皮质模式。