骨细胞对纯镁和 WE43 材料降解界面的影响:多模式体外分析的启示。

IF 9.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Diana C. Martinez , Anke Borkam-Schuster , Heike Helmholz , Anna Dobkowska , Bérengère Luthringer-Feyerabend , Tomasz Płociński , Regine Willumeit-Römer , Wojciech Święszkowski
{"title":"骨细胞对纯镁和 WE43 材料降解界面的影响:多模式体外分析的启示。","authors":"Diana C. Martinez ,&nbsp;Anke Borkam-Schuster ,&nbsp;Heike Helmholz ,&nbsp;Anna Dobkowska ,&nbsp;Bérengère Luthringer-Feyerabend ,&nbsp;Tomasz Płociński ,&nbsp;Regine Willumeit-Römer ,&nbsp;Wojciech Święszkowski","doi":"10.1016/j.actbio.2024.08.015","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, the interaction of pure Mg and WE43 alloy under the presence of osteoblast (OB) and osteoclast (OC) cells and their influence on the degradation of materials have been deeply analyzed. Since OB and OC interaction has an important role in bone remodeling, we examined the surface morphology and dynamic changes in the chemical composition and thickness of the corrosion layers formed on pure Mg and WE43 alloy by direct monoculture and coculture of pre-differentiated OB and OC cells <em>in vitro</em>. Electrochemical techniques examined the corrosion performance. The corrosion products were characterized using a combination of the focused ion beam (FIB), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). Cell viability and morphology were assessed by fluorescent microscopy and SEM. Our findings demonstrate cell spread and attachment variations, which differ depending on the Mg substrates. It was clearly shown that cell culture groups delayed degradation processes with the lowest corrosion rate observed in the presence of OBOC coculture for the WE43 substrate. Ca-P enrichment was observed in the outer-middle region of the corrosion layer but only after 7 days of OBOC coculture on WE43 and after 14 days on the pure Mg specimens.</div></div><div><h3>Statement of significance</h3><div>Magnesium metallic materials that can degrade over time provide distinct opportunities for orthopedic application. However, there is still a lack, especially in elucidating cell-material interface characterization. This study investigated the influence of osteoblast-osteoclast coculture in direct Mg-material contact. Our findings demonstrated that pre-differentiated osteoblasts and osteoclasts cocultured on Mg substrates influenced the chemistry of the corrosion layers. The cell spread and attachment were Mg substrate-dependent. The findings of coculturing bone cells directly on Mg materials within an <em>in vitro</em> model provide an effective approach for studying the dynamic degradation processes of Mg alloys while also elucidating cell behavior and their potential contribution to the degradation of these alloys.</div></div>","PeriodicalId":237,"journal":{"name":"Acta Biomaterialia","volume":"187 ","pages":"Pages 471-490"},"PeriodicalIF":9.4000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bone cells influence the degradation interface of pure Mg and WE43 materials: Insights from multimodal in vitro analysis\",\"authors\":\"Diana C. Martinez ,&nbsp;Anke Borkam-Schuster ,&nbsp;Heike Helmholz ,&nbsp;Anna Dobkowska ,&nbsp;Bérengère Luthringer-Feyerabend ,&nbsp;Tomasz Płociński ,&nbsp;Regine Willumeit-Römer ,&nbsp;Wojciech Święszkowski\",\"doi\":\"10.1016/j.actbio.2024.08.015\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this study, the interaction of pure Mg and WE43 alloy under the presence of osteoblast (OB) and osteoclast (OC) cells and their influence on the degradation of materials have been deeply analyzed. Since OB and OC interaction has an important role in bone remodeling, we examined the surface morphology and dynamic changes in the chemical composition and thickness of the corrosion layers formed on pure Mg and WE43 alloy by direct monoculture and coculture of pre-differentiated OB and OC cells <em>in vitro</em>. Electrochemical techniques examined the corrosion performance. The corrosion products were characterized using a combination of the focused ion beam (FIB), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). Cell viability and morphology were assessed by fluorescent microscopy and SEM. Our findings demonstrate cell spread and attachment variations, which differ depending on the Mg substrates. It was clearly shown that cell culture groups delayed degradation processes with the lowest corrosion rate observed in the presence of OBOC coculture for the WE43 substrate. Ca-P enrichment was observed in the outer-middle region of the corrosion layer but only after 7 days of OBOC coculture on WE43 and after 14 days on the pure Mg specimens.</div></div><div><h3>Statement of significance</h3><div>Magnesium metallic materials that can degrade over time provide distinct opportunities for orthopedic application. However, there is still a lack, especially in elucidating cell-material interface characterization. This study investigated the influence of osteoblast-osteoclast coculture in direct Mg-material contact. Our findings demonstrated that pre-differentiated osteoblasts and osteoclasts cocultured on Mg substrates influenced the chemistry of the corrosion layers. The cell spread and attachment were Mg substrate-dependent. The findings of coculturing bone cells directly on Mg materials within an <em>in vitro</em> model provide an effective approach for studying the dynamic degradation processes of Mg alloys while also elucidating cell behavior and their potential contribution to the degradation of these alloys.</div></div>\",\"PeriodicalId\":237,\"journal\":{\"name\":\"Acta Biomaterialia\",\"volume\":\"187 \",\"pages\":\"Pages 471-490\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Biomaterialia\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1742706124004604\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Biomaterialia","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1742706124004604","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

摘要

本研究深入分析了纯镁和 WE43 合金在成骨细胞(OB)和破骨细胞(OC)存在下的相互作用及其对材料降解的影响。由于成骨细胞和破骨细胞的相互作用在骨重塑中具有重要作用,我们通过体外直接单培养和共培养预分化的成骨细胞和破骨细胞,研究了纯 Mg 和 WE43 合金的表面形态、化学成分和腐蚀层厚度的动态变化。电化学技术检测了腐蚀性能。结合使用聚焦离子束(FIB)、扫描电子显微镜(SEM)和能量色散 X 射线光谱(EDX)对腐蚀产物进行了表征。荧光显微镜和扫描电子显微镜对细胞活力和形态进行了评估。我们的研究结果表明,细胞的扩散和附着随镁基底的不同而变化。研究清楚地表明,细胞培养组延缓了降解过程,在有 OBOC 共培养的情况下,WE43 基质的腐蚀率最低。在腐蚀层的中外层区域观察到 Ca-P 富集,但只有在 WE43 基材上的 OBOC 共培养 7 天后和纯镁试样上的 OBOC 共培养 14 天后才观察到。意义说明:可随时间降解的镁金属材料为骨科应用提供了独特的机会。然而,在阐明细胞-材料界面特性方面仍存在不足。本研究调查了成骨细胞-破骨细胞共培养对镁材料直接接触的影响。我们的研究结果表明,在镁基底上共培养的预分化成骨细胞和破骨细胞会影响腐蚀层的化学性质。细胞的扩散和附着取决于镁基底。在体外模型中直接在镁材料上共培养骨细胞的研究结果为研究镁合金的动态降解过程提供了一种有效的方法,同时也阐明了细胞行为及其对这些合金降解的潜在贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bone cells influence the degradation interface of pure Mg and WE43 materials: Insights from multimodal in vitro analysis

Bone cells influence the degradation interface of pure Mg and WE43 materials: Insights from multimodal in vitro analysis
In this study, the interaction of pure Mg and WE43 alloy under the presence of osteoblast (OB) and osteoclast (OC) cells and their influence on the degradation of materials have been deeply analyzed. Since OB and OC interaction has an important role in bone remodeling, we examined the surface morphology and dynamic changes in the chemical composition and thickness of the corrosion layers formed on pure Mg and WE43 alloy by direct monoculture and coculture of pre-differentiated OB and OC cells in vitro. Electrochemical techniques examined the corrosion performance. The corrosion products were characterized using a combination of the focused ion beam (FIB), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). Cell viability and morphology were assessed by fluorescent microscopy and SEM. Our findings demonstrate cell spread and attachment variations, which differ depending on the Mg substrates. It was clearly shown that cell culture groups delayed degradation processes with the lowest corrosion rate observed in the presence of OBOC coculture for the WE43 substrate. Ca-P enrichment was observed in the outer-middle region of the corrosion layer but only after 7 days of OBOC coculture on WE43 and after 14 days on the pure Mg specimens.

Statement of significance

Magnesium metallic materials that can degrade over time provide distinct opportunities for orthopedic application. However, there is still a lack, especially in elucidating cell-material interface characterization. This study investigated the influence of osteoblast-osteoclast coculture in direct Mg-material contact. Our findings demonstrated that pre-differentiated osteoblasts and osteoclasts cocultured on Mg substrates influenced the chemistry of the corrosion layers. The cell spread and attachment were Mg substrate-dependent. The findings of coculturing bone cells directly on Mg materials within an in vitro model provide an effective approach for studying the dynamic degradation processes of Mg alloys while also elucidating cell behavior and their potential contribution to the degradation of these alloys.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信