Blumer Michael J F, Schwarzer Christoph, Pérez Maria Teresa, Konakci Kadriye Zeynep, Fritsch Helga
Department of Anatomy, Histology and Embryology, Division of Clinical and Functional Anatomy, Medical University of Innsbruck, Austria.
J Anat. 2006 Jun;208(6):695-707. doi: 10.1111/j.1469-7580.2006.00578.x.
Osteoblasts and osteocytes derive from the same precursors, and osteocytes are terminally differentiated osteoblasts. These two cell types are distinguishable by their morphology, localization and levels of expression of various bone cell-specific markers. In the present study on the chicken femur we investigated the properties of the mesenchymal cells within cartilage canals on their course into the secondary ossification centre (SOC). We examined several developmental stages after hatching by means of light microscopy, electron microscopy, immunohistochemistry and in situ hybridization. Cartilage canals appeared as extensions of the perichondrium into the developing distal epiphysis and they were arranged in a complex network. Within the epiphysis an SOC was formed and cartilage canals penetrated into it. In addition, they were successively incorporated into the SOC during its growth in the radial direction. Thus, the canals provided this centre with mesenchymal cells and vessels. It should be emphasized that regression of cartilage canals could never be observed in the growing bone. Outside the SOC the mesenchymal cells of the canals expressed type I collagen and periostin and thus these cells had the characteristics of preosteoblasts. Periostin was also expressed by numerous chondrocytes. Within the SOC the synthesis of periostin was down-regulated and the majority of osteoblasts were periostin negative. Furthermore, osteocytes did not secret this protein. Tissue-non-specific alkaline phosphatase (TNAP) staining was only detectable where matrix vesicles were present. These vesicles were found around the blind end of cartilage canals within the SOC where newly formed osteoid started to mineralize. The vesicles originated from osteoblasts as well as from late osteoblasts/preosteocytes and thus TNAP was only expressed by these cells. Our results provide evidence that the mesenchymal cells of cartilage canals express various bone cell-specific markers depending on their position. We suggest that these cells differentiate from preosteoblasts into osteocytes on their course into the SOC and consider that cartilage canals are essential for normal bone development within the epiphysis. Furthermore, we propose that the expression of periostin by preosteoblasts and several chondrocytes is required for adhesion of these cells to the extracellular matrix.
成骨细胞和骨细胞来源于相同的前体细胞,骨细胞是终末分化的成骨细胞。这两种细胞类型可通过其形态、定位以及各种骨细胞特异性标志物的表达水平来区分。在本项关于鸡股骨的研究中,我们调查了软骨管内间充质细胞进入次级骨化中心(SOC)过程中的特性。我们通过光学显微镜、电子显微镜、免疫组织化学和原位杂交技术检查了孵化后的几个发育阶段。软骨管表现为软骨膜向发育中的远端骨骺的延伸,它们排列成复杂的网络。在骨骺内形成了一个SOC,软骨管穿透其中。此外,在其径向生长过程中,它们相继被纳入SOC。因此,这些管道为这个中心提供了间充质细胞和血管。应该强调的是,在生长的骨骼中从未观察到软骨管的退化。在SOC外部,管道的间充质细胞表达I型胶原蛋白和骨膜蛋白,因此这些细胞具有前成骨细胞的特征。许多软骨细胞也表达骨膜蛋白。在SOC内,骨膜蛋白的合成被下调,大多数成骨细胞为骨膜蛋白阴性。此外,骨细胞不分泌这种蛋白质。仅在存在基质小泡的地方可检测到组织非特异性碱性磷酸酶(TNAP)染色。这些小泡在SOC内软骨管的盲端周围被发现,在那里新形成的类骨质开始矿化。这些小泡起源于成骨细胞以及晚期成骨细胞/前骨细胞,因此TNAP仅由这些细胞表达。我们的结果提供了证据,表明软骨管的间充质细胞根据其位置表达各种骨细胞特异性标志物。我们认为这些细胞在进入SOC的过程中从前成骨细胞分化为骨细胞,并认为软骨管对于骨骺内正常的骨发育至关重要。此外,我们提出前成骨细胞和一些软骨细胞表达骨膜蛋白是这些细胞与细胞外基质粘附所必需的。