Pizette S, Niswander L
Memorial Sloan-Kettering Cancer Center, Molecular Biology Program and Howard Hughes Medical Institute, New York, New York, 10021, USA.
Dev Biol. 2000 Mar 15;219(2):237-49. doi: 10.1006/dbio.2000.9610.
Formation of the long bones requires a cartilage template. Cartilage formation (chondrogenesis) proceeds through determination of cells and their aggregation into prechondrogenic condensations, differentiation into chondrocytes, and later maturation. Several studies indicate that members of the bone morphogenetic protein (BMP) family promote cartilage formation, but the exact step(s) in which BMPs are involved during this process remains undefined. To resolve this issue, we have used a retroviral vector to misexpress the BMP antagonist Noggin in the embryonic chick limb. Unlike previous reports, we have characterized the resulting phenotype in depth, analyzing histological and early chondrogenic markers, as well as the patterns of cell death and proliferation. Misexpression of Noggin prior to the onset of chondrogenesis leads to the total absence of skeletal elements, as previously reported (J. Capdevila and R. L. Johnson, 1998, Dev. Biol. 197, 205-217). Noggin inhibits cartilage formation at two distinct steps. First, we demonstrate that mesenchymal cells do not aggregate into prechondrogenic condensations, and additional results suggest that these cells persist in an undifferentiated state. Second, we show that differentiation of chondroprogenitors into chondrocytes can also be blocked, concurrent with expanded expression of a presumptive joint region marker. In addition, we observed alterations in muscle and tendon morphogenesis, and the potential role of BMPs in these processes will be discussed. Our studies therefore provide in vivo evidence that BMPs are necessary for different steps of chondrogenesis: chondroprogenitor determination and/or condensation and subsequent differentiation into chondrocytes.
长骨的形成需要一个软骨模板。软骨形成(软骨发生)过程包括细胞的决定及其聚集形成前软骨凝聚物、分化为软骨细胞,随后成熟。多项研究表明,骨形态发生蛋白(BMP)家族成员促进软骨形成,但在此过程中BMP参与的确切步骤仍不明确。为了解决这个问题,我们使用逆转录病毒载体在胚胎鸡肢体中错误表达BMP拮抗剂Noggin。与之前的报道不同,我们深入研究了由此产生的表型,分析了组织学和早期软骨形成标志物,以及细胞死亡和增殖模式。如先前报道(J. Capdevila和R. L. Johnson,1998,《发育生物学》197,205 - 217),在软骨形成开始之前错误表达Noggin会导致骨骼元素完全缺失。Noggin在两个不同步骤抑制软骨形成。首先,我们证明间充质细胞不会聚集形成前软骨凝聚物,其他结果表明这些细胞维持在未分化状态。其次,我们表明软骨祖细胞向软骨细胞的分化也会被阻断,同时假定关节区域标志物的表达会扩大。此外,我们观察到肌肉和肌腱形态发生的改变,并将讨论BMP在这些过程中的潜在作用。因此,我们的研究提供了体内证据,表明BMP对于软骨发生的不同步骤是必需的:软骨祖细胞的决定和/或凝聚以及随后向软骨细胞的分化。