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Vascularization of primary and secondary ossification centres in the human growth plate

机译:人类生长板中主要和次生骨化中心的血管化

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摘要

BackgroundThe switch from cartilage template to bone during endochondral ossification of the growth plate requires a dynamic and close interaction between cartilage and the developing vasculature. Vascular invasion of the primarily avascular hypertrophic chondrocyte zone brings chondroclasts, osteoblast- and endothelial precursor cells into future centres of ossification.Vascularization of human growth plates of polydactylic digits was studied by immunohistochemistry, confocal-laser-scanning-microscopy and RT-qPCR using markers specific for endothelial cells CD34 and CD31, smooth muscle cells α-SMA, endothelial progenitor cells CD133, CXCR4, VEGFR-2 and mesenchymal progenitor cells CD90 and CD105. In addition, morphometric analysis was performed to quantify RUNX2+ and DLX5+ hypertrophic chondrocytes, RANK+ chondro- and osteoclasts, and CD133+ progenitors in different zones of the growth plate.
机译:背景技术在生长板的软骨内骨化过程中,从软骨模板向骨骼的转换需要软骨与发育中的脉管系统之间动态而紧密的相互作用。血管侵入主要是无血管的肥大软骨细胞区域,使软骨细胞,成骨细胞和内皮前体细胞进入未来的骨化中心。通过免疫组织化学,共聚焦激光扫描显微镜和使用标记的RT-qPCR研究了多指数字人类生长板的血管化对内皮细胞CD34和CD31,平滑肌细胞α-SMA,内皮祖细胞CD133,CXCR4,VEGFR-2和间充质祖细胞CD90和CD105具有特异性。此外,进行形态计量学分析以量化RUNX2 + 和DLX5 + 肥大软骨细胞,RANK + 软骨和破骨细胞以及CD133 + 祖先在生长板的不同区域。

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