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一种用于制备未经脱钙的骨软骨新鲜冷冻切片以进行元素映射和了解疾病病因的技术。

A technique for preparing undecalcified osteochondral fresh frozen sections for elemental mapping and understanding disease etiology.

机构信息

Centre for Biomedical Technologies, School of Mechanical, Medical and Process Engineering, Queensland University of Technology, 60 Musk Ave/cnr. Blamey St, Kelvin Grove, Brisbane, QLD, 4059, Australia.

Central Analytical Research Facility, Queensland University of Technology, Brisbane, 4059, Australia.

出版信息

Histochem Cell Biol. 2022 Nov;158(5):463-469. doi: 10.1007/s00418-022-02135-8. Epub 2022 Jul 9.

DOI:10.1007/s00418-022-02135-8
PMID:35809120
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9630180/
Abstract

The anatomy of the osteochondral junction is complex because several tissue components exist as a unit, including uncalcified cartilage (with superficial, middle, and deep layers), calcified cartilage, and subchondral bone. Furthermore, it is difficult to study because this region is made up of a variety of cell types and extracellular matrix compositions. Using X-ray fluorescence microscopy, we present a protocol for simultaneous elemental detection on fresh frozen samples. We transferred the osteochondral sample using a tape-assisted system and successfully tested it in synchrotron X-ray fluorescence. This protocol elucidates the distinct distribution of elements at the human knee's osteochondral junction, making it a useful tool for analyzing the co-distribution of various elements in both healthy and diseased states.

摘要

骨软骨连接的解剖结构很复杂,因为有几个组织成分作为一个单元存在,包括未钙化软骨(包括表层、中层和深层)、钙化软骨和软骨下骨。此外,由于该区域由多种细胞类型和细胞外基质组成,因此很难进行研究。我们使用 X 射线荧光显微镜,提出了一种对新鲜冷冻样本进行同时元素检测的方案。我们使用胶带辅助系统转移骨软骨样本,并在同步加速器 X 射线荧光中成功地对其进行了测试。该方案阐明了人膝关节骨软骨连接处元素的独特分布,使其成为分析健康和患病状态下各种元素共同分布的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/5198cb33a001/418_2022_2135_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/040393053fc3/418_2022_2135_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/d5cadbe97aca/418_2022_2135_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/5198cb33a001/418_2022_2135_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/040393053fc3/418_2022_2135_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/d5cadbe97aca/418_2022_2135_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a042/9630180/5198cb33a001/418_2022_2135_Fig3_HTML.jpg

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本文引用的文献

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Nano Lett. 2022 Mar 23;22(6):2309-2319. doi: 10.1021/acs.nanolett.1c04649. Epub 2022 Mar 3.
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The deterioration of calcified cartilage integrity reflects the severity of osteoarthritis-A structural, molecular, and biochemical analysis.钙化软骨完整性的恶化反映了骨关节炎的严重程度——结构、分子和生物化学分析。
FASEB J. 2022 Feb;36(2):e22142. doi: 10.1096/fj.202101449R.
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Preparation of Thin Frozen Sections from Nonfixed and Undecalcified Hard Tissues Using Kawamoto's Film Method (2020).
功能质谱成像在骨关节炎进展过程中绘制出磷脂酶 A2 酶的活性图。
Theranostics. 2023 Aug 21;13(13):4636-4649. doi: 10.7150/thno.86623. eCollection 2023.
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Spatial distribution of elements during osteoarthritis disease progression using synchrotron X-ray fluorescence microscopy.应用同步辐射 X 射线荧光显微镜研究骨关节炎疾病进展过程中的元素空间分布。
Sci Rep. 2023 Jun 23;13(1):10200. doi: 10.1038/s41598-023-36911-w.
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In focus in HCB.聚焦于六氯苯。
Histochem Cell Biol. 2022 Nov;158(5):411-414. doi: 10.1007/s00418-022-02160-7.
用川本氏薄膜法制备非固定和未脱钙硬组织的薄冰冻切片(2020)。
Methods Mol Biol. 2021;2230:259-281. doi: 10.1007/978-1-0716-1028-2_15.
4
Molecular Signaling Interactions and Transport at the Osteochondral Interface: A Review.骨软骨界面的分子信号相互作用与转运:综述
Front Cell Dev Biol. 2020 Aug 19;8:750. doi: 10.3389/fcell.2020.00750. eCollection 2020.
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The XFM beamline at the Australian Synchrotron.澳大利亚同步加速器的XFM光束线。
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