Stage-specific and location-specific cartilage calcification in osteoarthritis development

软骨 钙化 骨关节炎 医学 透射电子显微镜 病理 能量色散X射线光谱学 扫描电子显微镜 生物医学工程 材料科学 解剖 纳米技术 复合材料 替代医学
作者
Xiaozhao Wang,Qin Wu,Ru Zhang,Fan Zhang,Wenyue Li,Renwei Mao,Zihao Du,Xudong Yao,Yihua Ma,Yiyang Yan,Wei Sun,Hongwei Wu,Wei Wei,Yin Hu,Yi Hong,Huan Hu,Yi Wen Koh,Wei Duan,Xiao Chen,Hongwei Ouyang
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:82 (3): 393-402 被引量:12
标识
DOI:10.1136/ard-2022-222944
摘要

This study investigated the stage-specific and location-specific deposition and characteristics of minerals in human osteoarthritis (OA) cartilages via multiple nano-analytical technologies.Normal and OA cartilages were serially sectioned for micro-CT, scanning electron microscopy with energy dispersive X-ray spectroscopy, micro-Raman spectroscopy, focused ion beam scanning electron microscopy, high-resolution electron energy loss spectrometry with transmission electron microscopy, nanoindentation and atomic force microscopy to analyse the structural, compositional and mechanical properties of cartilage in OA progression.We found that OA progressed by both top-down calcification at the joint surface and bottom-up calcification at the osteochondral interface. The top-down calcification process started with spherical mineral particle formation in the joint surface during early-stage OA (OA-E), followed by fibre formation and densely packed material transformation deep into the cartilage during advanced-stage OA (OA-A). The bottom-up calcification in OA-E started when an excessive layer of calcified tissue formed above the original calcified cartilage, exhibiting a calcified sandwich structure. Over time, the original and upper layers of calcified cartilage fused, which thickened the calcified cartilage region and disrupted the cartilage structure. During OA-E, the calcified cartilage was hypermineralised, containing stiffer carbonated hydroxyapatite (HAp). During OA-A, it was hypomineralised and contained softer HAp. This discrepancy may be attributed to matrix vesicle nucleation during OA-E and carbonate cores during OA-A.This work refines our current understanding of the mechanism underlying OA progression and provides the foothold for potential therapeutic targeting strategies once the location-specific cartilage calcification features in OA are established.
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