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可视骨骼 2.0:基于 X 射线微计算机断层扫描的固定脊椎动物胚胎和胎儿软骨和骨的表型分析。

The visible skeleton 2.0: phenotyping of cartilage and bone in fixed vertebrate embryos and foetuses based on X-ray microCT.

机构信息

Histology and Embryology, Department for Pathobiology, University of Veterinary Medicine Vienna, Veterinärplatz 1, A-1210 Vienna, Austria.

Institute of Laboratory Animal Science, University of Veterinary Medicine Vienna, Veterinaärplatz 1, A-1210 Vienna, Austria.

出版信息

Development. 2020 May 29;147(11):dev187633. doi: 10.1242/dev.187633.

Abstract

For decades, clearing and staining with Alcian Blue and Alizarin Red has been the gold standard to image vertebrate skeletal development. Here, we present an alternate approach to visualise bone and cartilage based on X-ray microCT imaging, which allows the collection of genuine 3D data of the entire developing skeleton at micron resolution. Our novel protocol is based on ethanol fixation and staining with Ruthenium Red, and efficiently contrasts cartilage matrix, as demonstrated in whole E16.5 mouse foetuses and limbs of E14 chicken embryos. Bone mineral is well preserved during staining, thus the entire embryonic skeleton can be imaged at high contrast. Differences in X-ray attenuation of ruthenium and calcium enable the spectral separation of cartilage matrix and bone by dual energy microCT (microDECT). Clearing of specimens is not required. The protocol is simple and reproducible. We demonstrate that cartilage contrast in E16.5 mouse foetuses is adequate for fast visual phenotyping. Morphometric skeletal parameters are easily extracted. We consider the presented workflow to be a powerful and versatile extension to the toolkit currently available for qualitative and quantitative phenotyping of vertebrate skeletal development.

摘要

几十年来,使用阿利新蓝和茜素红进行清除和染色一直是成像脊椎动物骨骼发育的金标准。在这里,我们提出了一种替代方法,基于 X 射线微计算机断层扫描成像来可视化骨骼和软骨,它允许以微米分辨率收集整个发育中骨骼的真实 3D 数据。我们的新方案基于乙醇固定和钌红染色,有效地对比了软骨基质,如整个 E16.5 小鼠胚胎和 E14 鸡胚胎的四肢所示。在染色过程中很好地保存了骨矿物质,因此可以对整个胚胎骨骼进行高对比度成像。钌和钙的 X 射线衰减差异使通过双能微计算机断层扫描(microDECT)实现软骨基质和骨的光谱分离。不需要对标本进行清除。该方案简单且可重复。我们证明,E16.5 小鼠胚胎中的软骨对比足以进行快速视觉表型分析。形态骨骼参数易于提取。我们认为所提出的工作流程是对目前用于脊椎动物骨骼发育定性和定量表型分析的工具包的强大而通用的扩展。

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