Duprez D, Bell E J, Richardson M K, Archer C W, Wolpert L, Brickell P M, Francis-West P H
Department of Molecular Pathology, University College London Medical School, UK.
Mech Dev. 1996 Jul;57(2):145-57. doi: 10.1016/0925-4773(96)00540-0.
Bone morphogenetic proteins are members of the transforming growth factor beta (TGF beta) superfamily which are involved in a range of developmental processes including modelling of the skeleton. We show here that Bmp-2 is expressed in mesenchyme surrounding early cartilage condensations in the developing chick limb, and that Bmp-4 is expressed in the perichondrium of developing cartilage elements. To investigate their roles during cartilage development, BMP-2 and BMP-4 were expressed ectopically in developing chick limbs using retroviral vectors. Over-expression of BMP-2 or BMP-4 led to a dramatic increase in the volume of cartilage elements, altered their shapes and led to joint fusions. This increase in volume appeared to result from an increase in the amount of matrix and in the number of chondrocytes. The latter did not appear to be due to increased proliferation of chondrocytes, suggesting that it may result from increased recruitment of precursors. BMP-2 and BMP-4 also delayed hypertrophy of chondrocytes and formation of the osteogenic periosteum. These data provide insights into how BMP-2 and BMP-4 may model and control the growth of skeletal elements during normal embryonic development, suggesting roles for both molecules in recruiting non-chondrogenic precursors to chondrogenic fate.
骨形态发生蛋白是转化生长因子β(TGFβ)超家族的成员,参与一系列发育过程,包括骨骼的塑形。我们在此表明,Bmp-2在发育中的鸡胚肢体早期软骨凝聚周围的间充质中表达,而Bmp-4在发育中的软骨元件的软骨膜中表达。为了研究它们在软骨发育过程中的作用,使用逆转录病毒载体在发育中的鸡胚肢体中异位表达BMP-2和BMP-4。BMP-2或BMP-4的过表达导致软骨元件体积急剧增加,改变其形状并导致关节融合。这种体积增加似乎是由于基质数量和软骨细胞数量增加所致。后者似乎不是由于软骨细胞增殖增加,这表明它可能是由于前体细胞招募增加所致。BMP-2和BMP-4还延迟了软骨细胞的肥大和成骨骨膜的形成。这些数据为BMP-2和BMP-4在正常胚胎发育过程中如何塑造和控制骨骼元件的生长提供了见解,表明这两种分子在将非软骨生成前体细胞招募到软骨生成命运中发挥作用。