Riminucci M, Bradbeer J N, Corsi A, Gentili C, Descalzi F, Cancedda R, Bianco P
Dipartimento di Medicina Sperimentale, Università La Sapienza, Roma, Italy.; Dipartimento di Medicina Sperimentale, Università dell'Aquila, L' Aquila, Italy.
J Bone Miner Res. 1998 Dec;13(12):1852-61. doi: 10.1359/jbmr.1998.13.12.1852.
Bone formation throughout skeletal growth and remodeling always entails deposition of new bone onto a pre-existing mineralized surface. In contrast, the initial deposition of bone in development requires the formation, ex novo, of the first mineralized structure in a nonmineralized tissue. We investigated the cellular events associated with this initial bone formation, with specific reference to the respective role of cartilage and bone cells in bones which form via a cartilage model. The cellular architecture of initial osteogenic sites was investigated by light, confocal, and electron microscopy (EM) in the membranous ossification of fetal calvarial bones (not forming via a cartilage model) and in the membranous ossification of the bony collars of endochondral bones. Bone sialoprotein (BSP), which is expressed during early phases of bone deposition and has been proposed to be involved in the control of both mineral formation and bone cell-matrix interactions, was used as a marker of initial bone formation. We found that at all sites, BSP-producing cells (as identified by intracellular immunoreactivity) are arranged in a characteristic vis-à-vis (face to face) pattern prior to the appearance of the first mineralizing BSP-immunoreactive extracellular matrix. In perichondral osteogenesis, the vis-à-vis pattern comprises osteoblasts differentiating from the perichondrium/periosteum and early hypertrophic chondrocytes located at the lateral aspects of the rudiment. By EM, the first mineral and the first BSP-immunoreactive sites coincide temporally and spatially in the extracellular matrix at the boundary between cartilage and periosteum. We further showed that in an in vitro avian model of chondrocyte differentiation in vitro to osteoblast-like cells, early hypertrophic chondrocytes replated as adherent cells turned on the expression of high levels of BSP in conjunction with the switch to collagen type I synthesis and matrix mineralization. We propose a model for the priming of bone deposition, i.e., the formation of the first bone structure, in which the architectural layout of cells competent to deposit a mineralizing matrix (the vis-à-vis pattern) determines the polarized deposition of bone. For bones forming via a cartilage model, the priming of bone deposition involves and requires cells that differentiate from early hypertrophic chondrocytes.
在整个骨骼生长和重塑过程中,骨形成总是需要在预先存在的矿化表面上沉积新骨。相比之下,发育过程中骨的初始沉积需要在非矿化组织中从头形成第一个矿化结构。我们研究了与这种初始骨形成相关的细胞事件,特别参考了软骨和骨细胞在通过软骨模型形成的骨骼中的各自作用。通过光学显微镜、共聚焦显微镜和电子显微镜(EM)研究了胎儿颅骨膜内成骨(不通过软骨模型形成)和软骨内骨骨领膜内成骨中初始成骨部位的细胞结构。骨唾液蛋白(BSP)在骨沉积的早期阶段表达,并被认为参与矿物质形成和骨细胞 - 基质相互作用的控制,被用作初始骨形成的标志物。我们发现,在所有部位,产生BSP的细胞(通过细胞内免疫反应鉴定)在第一个矿化的BSP免疫反应性细胞外基质出现之前,以特征性的面对面模式排列。在软骨膜成骨中,面对面模式包括从软骨膜/骨膜分化而来的成骨细胞和位于原基侧面的早期肥大软骨细胞。通过电子显微镜观察,第一个矿物质和第一个BSP免疫反应性位点在软骨和骨膜之间边界处的细胞外基质中在时间和空间上重合。我们进一步表明,在体外软骨细胞分化为成骨样细胞的禽类模型中,重新接种为贴壁细胞的早期肥大软骨细胞在转换为I型胶原合成和基质矿化的同时开启了高水平BSP的表达。我们提出了一个骨沉积启动模型,即第一个骨结构的形成,其中能够沉积矿化基质的细胞的结构布局(面对面模式)决定了骨的极化沉积。对于通过软骨模型形成的骨骼,骨沉积的启动涉及并需要从早期肥大软骨细胞分化而来的细胞。