Takahara Masatoshi, Harada Mikio, Guan Dehong, Otsuji Miwako, Naruse Takuji, Takagi Michiaki, Ogino Toshihiko
Department of Orthopaedic Surgery, Yamagata University School of Medicine, Yamagata 990-9585, Japan.
Bone. 2004 Nov;35(5):1069-76. doi: 10.1016/j.bone.2004.06.020.
Growth/differentiation factor 5 (GDF5) is a member of the bone morphogenetic protein (BMP) family, which has been implicated in several skeletogenic events including cartilage and bone formation. To study the role of GDF5, we analyzed digit development in brachypodism (bp) mice, which carry functional null mutations of the Gdf5 gene and exhibit a reduction in the length of digit bones and loss of the middle phalanges. In situ detection of apoptosis and whole-mount detection of cell death showed abnormal apoptosis in the developing phalanges of bp mice. In situ hybridization in bp mice showed overexpression of Gdf5 mRNA in the developing phalanges where apoptotic cells were increased. In addition, bp mice exhibited excessive apoptosis in the interdigital regions. The condensed mesenchymal cells were progressively decreased in the developing phalanges and failed to form cartilage models of the middle phalanges. These findings show that excessive apoptosis in the absence of GDF5 results in developmental failure of the phalanges. We conclude that GDF5 is essential for maintenance and growth of the developing phalanges.
生长/分化因子5(GDF5)是骨形态发生蛋白(BMP)家族的成员,它与包括软骨和骨形成在内的多个骨骼发生事件有关。为了研究GDF5的作用,我们分析了短肢(bp)小鼠的指发育情况,这些小鼠携带Gdf5基因的功能性无效突变,表现为指骨长度缩短和中节指骨缺失。凋亡的原位检测和细胞死亡的整体检测显示,bp小鼠发育中的指骨存在异常凋亡。bp小鼠的原位杂交显示,在凋亡细胞增加的发育中的指骨中,Gdf5 mRNA过度表达。此外,bp小鼠在指间区域表现出过度凋亡。在发育中的指骨中,浓缩的间充质细胞逐渐减少,无法形成中节指骨的软骨模型。这些发现表明,在缺乏GDF5的情况下,过度凋亡导致指骨发育失败。我们得出结论,GDF5对于发育中手指的维持和生长至关重要。