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质子和碳离子辐照改变体外股骨器官培养模型的软骨内骨化过程。

Proton and Carbon Ion Irradiation Changes the Process of Endochondral Ossification in an Ex Vivo Femur Organotypic Culture Model.

机构信息

Department of Orthopaedics and Trauma, Medical University Graz, 8036 Graz, Austria.

Department of Neurosurgery, Research Unit for Experimental Neurotraumatology, Medical University of Graz, 8036 Graz, Austria.

出版信息

Cells. 2023 Sep 18;12(18):2301. doi: 10.3390/cells12182301.

DOI:10.3390/cells12182301
PMID:37759523
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10527791/
Abstract

Particle therapy (PT) that utilizes protons and carbon ions offers a promising way to reduce the side effects of radiation oncology, especially in pediatric patients. To investigate the influence of PT on growing bone, we exposed an organotypic rat ex vivo femur culture model to PT. After irradiation, histological staining, immunohistochemical staining, and gene expression analysis were conducted following 1 or 14 days of in vitro culture (DIV). Our data indicated a significant loss of proliferating chondrocytes at 1 DIV, which was followed by regeneration attempts through chondrocytic cluster formation at 14 DIV. Accelerated levels of mineralization were observed, which correlated with increased proteoglycan production and secretion into the pericellular matrix. Col2α1 expression, which increased during the cultivation period, was significantly inhibited by PT. Additionally, the decrease in ColX expression over time was more pronounced compared to the non-IR control. The chondrogenic markers BMP2, RUNX2, OPG, and the osteogenic marker ALPL, showed a significant reduction in the increase in expression after 14 DIV due to PT treatment. It was noted that carbon ions had a stronger influence than protons. Our bone model demonstrated the occurrence of pathological and regenerative processes induced by PT, thus building on the current understanding of the biological mechanisms of bone.

摘要

粒子治疗(PT)利用质子和碳离子为减少放射肿瘤学的副作用提供了一种有前途的方法,特别是在儿科患者中。为了研究 PT 对生长中骨骼的影响,我们将体外培养的大鼠同种异体股骨模型暴露于 PT 下。照射后,进行组织学染色、免疫组织化学染色和基因表达分析,分别在体外培养 1 天(DIV)和 14 天(DIV)后进行。我们的数据表明,在 1 DIV 时增殖的软骨细胞明显减少,随后在 14 DIV 时通过软骨细胞簇形成进行再生尝试。观察到矿化加速,与细胞外基质中蛋白聚糖的产生和分泌增加相关。Col2α1 表达在培养期间增加,但被 PT 显著抑制。此外,与非 IR 对照相比,ColX 表达随时间的下降更为明显。软骨形成标志物 BMP2、RUNX2、OPG 和成骨标志物 ALPL 的表达在 14 DIV 后由于 PT 处理而增加减少。值得注意的是,碳离子的影响比质子更强。我们的骨模型显示了由 PT 引起的病理性和再生过程的发生,从而为骨骼的生物学机制的现有理解提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/2cd937045138/cells-12-02301-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/6ed974a499cb/cells-12-02301-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/bc87044c6698/cells-12-02301-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/10ccd0577bd0/cells-12-02301-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/21621e906a0e/cells-12-02301-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/36d3b9b709ba/cells-12-02301-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/2cd937045138/cells-12-02301-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/6ed974a499cb/cells-12-02301-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/bc87044c6698/cells-12-02301-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/10ccd0577bd0/cells-12-02301-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/21621e906a0e/cells-12-02301-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/36d3b9b709ba/cells-12-02301-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/10527791/2cd937045138/cells-12-02301-g006.jpg

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本文引用的文献

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The ATR Inhibitor VE-821 Enhances the Radiosensitivity and Suppresses DNA Repair Mechanisms of Human Chondrosarcoma Cells.ATR 抑制剂 VE-821 增强人软骨肉瘤细胞的放射敏感性并抑制其 DNA 修复机制。
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Multicolor Histochemical Staining for Identification of Mineralized and Non-Mineralized Musculoskeletal Tissue: Immunohistochemical and Radiological Validation in Decalcified Bone Samples.
用于识别矿化和非矿化肌肉骨骼组织的多色组织化学染色:脱钙骨样本的免疫组织化学和放射学验证
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