鸡胚软骨管参与骨骺生长板软骨内成骨过程。

Michael J F Blumer, Stefano Longato, Helga Fritsch
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引用次数: 29

摘要

对所谓的通讯软骨管进行了详细的研究,目的是阐明这些通道是否参与骨形成过程,这些通道深入到胚胎鸡股骨(E20)骺生长板的下增厚区。此外,我们检查了软骨管形成的方式,并将目前的数据与我们以前的数据进行比较。通过光镜、电镜、免疫组化(VEGF、VEGFR2/Flk1、I型胶原)和3D重建对管道进行研究。一些通信管道深入到上部肥厚带,在其末端显示电子密集细胞。这些细胞的亚细胞特征很难检测到,我们认为它们经历了细胞死亡。其他的管道则向下深入到较低的肥厚带。这些管道的上段由毛细血管、间充质细胞和巨噬细胞样细胞组成。成骨细胞的前体位于椎管附近。交通管下段由骨基质或类骨组成,其中含有I型胶原原纤维和具有成骨细胞典型亚细胞特征的细胞。这些节段内没有血管。免疫组织化学显示,管道基质阳性标记为I型胶原。此外,天狼星红染色显示这些部位形成骨基质。我们认为交通管下部的成骨细胞样细胞来源于间充质细胞或肥大软骨细胞。我们的免疫组织化学数据还显示,血管内皮生长因子(VEGF)和相应的受体VEGFR2/Flk1 (VEGF受体2/Flk1)定位于储备区、增殖区和肥厚区软骨管中。受体存在于血管内皮细胞中。此外,VEGF存在于肥大软骨细胞中。我们的研究结果表明,软骨管主动渗透到软骨基质中,骨形成于交通管的下部,那里没有血管可检测到。
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Cartilage canals in the chicken embryo are involved in the process of endochondral bone formation within the epiphyseal growth plate.

A detailed study of so-called communicating cartilage canals, which penetrate deeply up into the lower hypertrophic zone of the epiphyseal growth plate in the embryonic chicken femur (E20), was carried out with the aim to clarify whether or not these canals are involved in the bone-forming process. In addition, we examined the manner in which cartilage canals are formed and compare the present data with our previous data. The canals were investigated by means of light microscopy, electron microscopy, immunohistochemistry (VEGF, VEGFR2/Flk1, type I collagen), and 3D reconstruction. Some communicating canals deeply penetrate into the upper hypertrophic zone where they terminate, showing electron-dense cells at their end. Subcellular characteristics of these cells are hardly detectable and we suppose that they undergo cell death. Other canals pass down deeper into the lower hypertrophic zone. The upper segment of these canals is composed of capillaries, mesenchymal cells, and macrophage-like cells. Precursors of osteoblasts are adjacent to the canals. The lower segment of communicating canals is composed of bone matrix or osteoid, which contains type I collagen fibrils and cells having the typical subcellular features of osteoblasts. No vessels are found in these segments. Immunohistochemistry shows that the matrix of the canals labels positively for type I collagen. In addition, staining with sirius red demonstrates that bone matrix is formed in these parts. We assume that the osteoblast-like cells of the lower segments of communicating canals originate either from mesenchymal cells or even from hypertrophic chondrocytes. Our immunohistochemical data also reveal that vascular endothelial growth factor (VEGF) and the corresponding receptor VEGFR2/Flk1 (VEGF receptor 2/Flk1) are localized in cartilage canals of the reserve zone, the proliferative zone, and the hypertrophic zone. The receptor is found in the endothelial cells of the vessels. Furthermore, VEGF is present in hypertrophic chondrocytes. The results of our study suggest that cartilage canals penetrate actively into the cartilage anlage and that bone is formed in the lower segments of the communicating canals where no vessels are detectable.

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