Raymond Purves Bone and Joint Research Laboratories, Institute of Bone and Joint Research, The Kolling Institute of Medical Research, University of Sydney at Royal North Shore Hospital, Level 10, Building B6, St. Leonards, NSW 2065, Australia.
Eur Spine J. 2013 Aug;22(8):1774-84. doi: 10.1007/s00586-013-2680-1. Epub 2013 Feb 10.
A comparative immunolocalisation study of perlecan, HS, FGF-18 and FGFR-3 in the 12-20-week gestational age human foetal spine was undertaken to identify spatiotemporal associations between these components to provide insights into prospective roles in spinal development.
Comparative immunolocalisations of matrix and cell associated components in Histochoice-fixed paraffin-embedded human foetal spinal tissues.
The 12-14-week-old human foetal spine was a predominantly cartilaginous structure with the discs displaying a relative paucity of proteoglycan compared to the adjacent cartilaginous vertebral rudiments, notochordal remnants were also observed. HS and perlecan had a widespread distribution throughout the spine at 12 weeks, however, FGF-18 was only localised to the outer AF margins and hypertrophic cell condensations in the vertebral bodies. This contrasted with HS distributions at 14-20 weeks, which were prominent in the developing intervertebral disc (IVD). Ossification centres were also evident centrally within the vertebral rudiments surrounded by small columns of hypertrophic chondrocytes which expressed FGFR-3 and FGF-18 and upregulated levels of perlecan. FGF-18 also had a prominent localisation pattern in the developing IVD and the cartilaginous endplate while FGFR-3 was expressed throughout the disc interspace. This suggested roles for perlecan, FGF-18 and FGFR-3 in chondrogenic and osteogenic events which drive discal development and ossification of the vertebral bodies.
The above data supported a role for FGF-18 in discal development and in the terminal osteogenic differentiation of chondroprogenitor cell populations, which promote vertebral ossification during spinal development.
对 12-20 周龄人类胎儿脊柱中的 PG、HS、FGF-18 和 FGFR-3 进行比较免疫定位研究,以确定这些成分之间的时空关联,从而深入了解其在脊柱发育中的潜在作用。
对 Histochoice 固定的石蜡包埋人胎儿脊柱组织中的基质和细胞相关成分进行比较免疫定位。
12-14 周龄的人类胎儿脊柱主要为软骨结构,与相邻的软骨性椎骨原基相比,椎间盘的蛋白聚糖相对较少,也观察到脊索残余物。12 周时,HS 和 perlecan 在整个脊柱中广泛分布,然而,FGF-18 仅局限于 AF 边缘的外侧和椎体的肥大细胞凝聚处。这与 14-20 周时 HS 的分布形成对比,HS 在发育中的椎间盘(IVD)中分布明显。骨化中心也在椎骨原基的中央明显可见,周围是表达 FGFR-3 和 FGF-18 并上调 perlecan 水平的肥大软骨细胞小柱。FGF-18 在发育中的 IVD 和软骨终板中也有明显的定位模式,而 FGFR-3 则在整个椎间盘间隙中表达。这表明 perlecan、FGF-18 和 FGFR-3 在软骨生成和骨生成事件中发挥作用,这些事件驱动椎间盘发育和椎体骨化。
上述数据支持 FGF-18 在椎间盘发育和软骨祖细胞群体的终末成骨分化中的作用,这促进了脊柱发育过程中的椎体骨化。