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首页> 外文期刊>Journal of the Royal Society Interface >Collagen reorganization in cartilage under strain probed by polarization sensitive second harmonic generation microscopy
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Collagen reorganization in cartilage under strain probed by polarization sensitive second harmonic generation microscopy

机译:通过偏振敏敏次级谐波产生显微镜探测菌株的软骨中的胶原蛋白重组

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摘要

Type II collagen fibril diameters in cartilage are beneath the diffraction limit of optical microscopy, which makes the assessment of collagen organization very challenging. In this work we use polarization sensitive second harmonic generation (P-SHG) imaging to map collagen organization in articular cartilage, addressing in particular its behaviour under strain and changes which occur in osteoarthritis. P-SHG yields two parameters, molecular order and orientation, which provide measures of the degree of organization both at the molecular scale (below the diffraction limit) and above a few hundred nanometres (at the image pixel size). P-SHG clearly demonstrates the zonal collagen architecture and reveals differences in the structure of the fibrils around chondrocytes. P-SHG also reveals sub-micron scale fibril re-organization in cartilage strips exposed to tensile loading, with an increase in local organization in the superficial zone which weakly correlates with tensile modulus. Finally, P-SHG is used to investigate osteoarthritic cartilage from total knee replacement surgery, and reveals widespread heterogeneity across samples both microscale fibril orientations and their sub-micron organization. By addressing collagen fibril structure on scales intermediate between conventional light and electron microscopy, this study provides new insights into collagen micromechanics and mechanisms of degradation.
机译:软骨中的II型胶原纤维直径位于光学显微镜的衍射极限下,这使得对胶原蛋白组织的评估非常具有挑战性。在这项工作中,我们使用偏振敏感的第二次谐波产生(P-SHG)成像来映射关节软骨中的胶原蛋白组织,特别是其在骨关节炎中发生的应变和变化的行为。 P-SHG产生两种参数,分子阶和取向,其在分子尺度(衍射极限下方)和几百纳米上方(在图像像素尺寸下)提供组织程度的测量。 P-SHG清楚地展示了区内胶原型架构,并揭示了细胞内纤维纤维结构的差异。 P-SHG还揭示了暴露于拉伸载荷的软骨条带中的亚微米级纤维细胞,其局部组织与拉伸模量略微相关。最后,P-SHG用于从全膝关节置换手术中探讨骨关节炎软骨,并揭示了微观纤维取向及其亚微米组织的样品的广泛的异质性。通过在常规光和电子显微镜间之间的尺度中间地址胶原纤维结构,本研究为胶原蛋白微机械和降解机制提供了新的见解。

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