• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

镁-钙-锶合金降解产物对人骨髓间充质干细胞的影响。

The effect of Mg-Ca-Sr alloy degradation products on human mesenchymal stem cells.

机构信息

Department of Materials Science and Engineering, University of Florida, Gainesville, Florida, 32611.

Department of Biomedical Engineering, University of Florida, Gainesville, Florida, 32611.

出版信息

J Biomed Mater Res B Appl Biomater. 2018 Feb;106(2):697-704. doi: 10.1002/jbm.b.33869. Epub 2017 Mar 21.

DOI:10.1002/jbm.b.33869
PMID:28323384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5811831/
Abstract

Biodegradable Mg alloys have the potential to replace currently used metallic medical implant devices, likely eliminating toxicity concerns and the need for secondary surgeries, while also providing a potentially stimulating environment for tissue growth. A recently developed Mg-Ca-Sr alloy possesses advantageous characteristics over other Mg alloys, having a good combination of strength and degradation behavior, while also displaying potentially osteogenic properties. To better understand the effect of alloy degradation products on cellular mechanisms, in vitro studies using human bone marrow-derived mesenchymal stem cells were conducted. Ionic products of alloy dissolution were found to be nontoxic but changed the proliferation profile of stem cells. Furthermore, their presence changed the progress of osteogenic development, while concentrations of Mg in particular appeared to induce stem cell differentiation. The work presented herein provides a foundation for future alloy design where structures can be tailored to obtain specific implant performance. These potentially bioactive implants would reduce the risks for patients by shortening their healing time, minimizing discomfort and toxicity concerns, while reducing hospital costs. © 2017 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 697-704, 2018.

摘要

可生物降解的 Mg 合金有可能替代目前使用的金属医学植入物,这可能消除了毒性问题和二次手术的需要,同时也为组织生长提供了一个潜在的刺激环境。最近开发的 Mg-Ca-Sr 合金与其他 Mg 合金相比具有优势,具有良好的强度和降解行为的结合,同时也具有潜在的成骨性能。为了更好地了解合金降解产物对细胞机制的影响,进行了使用人骨髓间充质干细胞的体外研究。发现合金溶解的离子产物没有毒性,但改变了干细胞的增殖谱。此外,它们的存在改变了成骨发育的进程,而特别是 Mg 的浓度似乎诱导了干细胞分化。本文所介绍的工作为未来的合金设计提供了基础,在这种设计中,可以调整结构以获得特定的植入物性能。这些潜在的生物活性植入物将通过缩短愈合时间、最小化不适和毒性问题以及降低医院成本来降低患者的风险。 © 2017 作者 生物医学材料研究杂志 B 部分:应用生物材料 由 Wiley 期刊出版公司出版 J 生物医学材料研究杂志 B: Appl Biomater, 106B: 697-704, 2018.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/fa6cd1d5f402/JBM-106-697-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/d2f77fe47df0/JBM-106-697-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/5447f7942ae1/JBM-106-697-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/11657302dd4c/JBM-106-697-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/fa6cd1d5f402/JBM-106-697-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/d2f77fe47df0/JBM-106-697-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/5447f7942ae1/JBM-106-697-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/11657302dd4c/JBM-106-697-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9569/5811831/fa6cd1d5f402/JBM-106-697-g004.jpg

相似文献

1
The effect of Mg-Ca-Sr alloy degradation products on human mesenchymal stem cells.镁-钙-锶合金降解产物对人骨髓间充质干细胞的影响。
J Biomed Mater Res B Appl Biomater. 2018 Feb;106(2):697-704. doi: 10.1002/jbm.b.33869. Epub 2017 Mar 21.
2
In vitro evaluation of MgSr and MgCaSr alloys via direct culture with bone marrow derived mesenchymal stem cells.骨髓间充质干细胞直接培养法对 MgSr 和 MgCaSr 合金的体外评价
Acta Biomater. 2018 May;72:407-423. doi: 10.1016/j.actbio.2018.03.049. Epub 2018 Apr 5.
3
An in vivo study on the metabolism and osteogenic activity of bioabsorbable Mg-1Sr alloy.生物可吸收Mg-1Sr合金代谢与成骨活性的体内研究
Acta Biomater. 2016 Jan;29:455-467. doi: 10.1016/j.actbio.2015.11.014. Epub 2015 Nov 11.
4
Human mesenchymal stem cells differentiate into an osteogenic lineage in presence of strontium containing bioactive glass nanoparticles.含锶生物活性玻璃纳米粒子诱导人骨髓间充质干细胞向成骨细胞系分化。
Acta Biomater. 2019 May;90:373-392. doi: 10.1016/j.actbio.2019.03.038. Epub 2019 Mar 23.
5
Ag-loaded MgSrFe-layered double hydroxide/chitosan composite scaffold with enhanced osteogenic and antibacterial property for bone engineering tissue.载银镁锶铁层状双氢氧化物/壳聚糖复合支架,具有增强的成骨和抗菌性能,用于骨工程组织。
J Biomed Mater Res B Appl Biomater. 2018 Feb;106(2):863-873. doi: 10.1002/jbm.b.33900. Epub 2017 Apr 17.
6
Mechanical properties, corrosion, and biocompatibility of Mg-Zr-Sr-Dy alloys for biodegradable implant applications.用于可生物降解植入物应用的 Mg-Zr-Sr-Dy 合金的力学性能、腐蚀和生物相容性。
J Biomed Mater Res B Appl Biomater. 2018 Aug;106(6):2425-2434. doi: 10.1002/jbm.b.34051. Epub 2017 Nov 28.
7
Bone tissue engineering strategy based on the synergistic effects of silicon and strontium ions.基于硅离子和锶离子协同作用的骨组织工程策略。
Acta Biomater. 2018 May;72:381-395. doi: 10.1016/j.actbio.2018.03.051. Epub 2018 Apr 6.
8
Cytocompatibility assessment of Ti-Zr-Pd-Si-(Nb) alloys with low Young's modulus, increased hardness, and enhanced osteoblast differentiation for biomedical applications.用于生物医学应用的低杨氏模量、高硬度和增强成骨细胞分化的 Ti-Zr-Pd-Si-(Nb) 合金的细胞相容性评估。
J Biomed Mater Res B Appl Biomater. 2018 Feb;106(2):834-842. doi: 10.1002/jbm.b.33892. Epub 2017 Apr 8.
9
Regulation of osteogenesis and osteoclastogenesis by zoledronic acid loaded on biodegradable magnesium-strontium alloy.载唑来膦酸的可生物降解镁-锶合金对成骨和破骨细胞生成的调节作用。
Sci Rep. 2019 Jan 30;9(1):933. doi: 10.1038/s41598-018-37091-8.
10
In vitro and in vivo evaluation of novel biodegradable Mg-Ag-Y alloys for use as resorbable bone fixation implant.新型可生物降解 Mg-Ag-Y 合金作为可吸收性骨固定植入物的体外和体内评价。
J Biomed Mater Res A. 2018 Jul;106(7):2059-2069. doi: 10.1002/jbm.a.36397. Epub 2018 May 11.

引用本文的文献

1
Impact of Metal Ions on Cellular Functions: A Focus on Mesenchymal Stem/Stromal Cell Differentiation.金属离子对细胞功能的影响:以间充质干细胞/基质细胞分化为例。
Int J Mol Sci. 2024 Sep 20;25(18):10127. doi: 10.3390/ijms251810127.
2
An overview of magnesium-based implants in orthopaedics and a prospect of its application in spine fusion.镁基植入物在骨科领域的概述及其在脊柱融合中的应用前景。
Bioact Mater. 2024 May 30;39:456-478. doi: 10.1016/j.bioactmat.2024.04.026. eCollection 2024 Sep.
3
Corrosion Behavior in Magnesium-Based Alloys for Biomedical Applications.

本文引用的文献

1
Peri-implant tissue response and biodegradation performance of a Mg-1.0Ca-0.5Sr alloy in rat tibia.Mg-1.0Ca-0.5Sr合金在大鼠胫骨中的种植体周围组织反应及生物降解性能
Mater Sci Eng C Mater Biol Appl. 2016 May;62:79-85. doi: 10.1016/j.msec.2015.12.002. Epub 2015 Dec 3.
2
Proteomic analysis of the effect of extracellular calcium ions on human mesenchymal stem cells: Implications for bone tissue engineering.细胞外钙离子对人骨髓间充质干细胞影响的蛋白质组学分析及其在骨组织工程中的意义。
Chem Biol Interact. 2015 May 25;233:139-46. doi: 10.1016/j.cbi.2015.03.021. Epub 2015 Mar 28.
3
Use of RUNX2 expression to identify osteogenic progenitor cells derived from human embryonic stem cells.
用于生物医学应用的镁基合金的腐蚀行为
Materials (Basel). 2022 Apr 1;15(7):2613. doi: 10.3390/ma15072613.
4
Regulation of Magnesium Matrix Composites Materials on Bone Immune Microenvironment and Osteogenic Mechanism.镁基复合材料对骨免疫微环境的调控及成骨机制
Front Bioeng Biotechnol. 2022 Mar 14;10:842706. doi: 10.3389/fbioe.2022.842706. eCollection 2022.
5
Insights into the Role of Magnesium Ions in Affecting Osteogenic Differentiation of Mesenchymal Stem Cells.镁离子在影响间充质干细胞成骨分化中的作用研究进展。
Biol Trace Elem Res. 2021 Feb;199(2):559-567. doi: 10.1007/s12011-020-02183-y. Epub 2020 May 24.
6
Magnesium Is a Key Regulator of the Balance between Osteoclast and Osteoblast Differentiation in the Presence of Vitamin D₃.镁在维生素 D₃存在的情况下是调节破骨细胞和成骨细胞分化平衡的关键。
Int J Mol Sci. 2019 Jan 17;20(2):385. doi: 10.3390/ijms20020385.
7
[Effects of calcium ion on the migration and osteogenic differentiation of human osteoblasts].[钙离子对人成骨细胞迁移及成骨分化的影响]
Hua Xi Kou Qiang Yi Xue Za Zhi. 2018 Dec 1;36(6):602-608. doi: 10.7518/hxkq.2018.06.004.
8
Bone biomaterials and interactions with stem cells.骨生物材料及其与干细胞的相互作用。
Bone Res. 2017 Dec 21;5:17059. doi: 10.1038/boneres.2017.59. eCollection 2017.
利用 RUNX2 表达鉴定人胚胎干细胞来源的成骨祖细胞。
Stem Cell Reports. 2015 Feb 10;4(2):190-8. doi: 10.1016/j.stemcr.2015.01.008.
4
Strontium ranelate stimulates the activity of bone-specific alkaline phosphatase: interaction with Zn(2+) and Mg (2+).雷奈酸锶可刺激骨特异性碱性磷酸酶的活性:与锌离子(Zn(2+))和镁离子(Mg(2+))的相互作用。
Biometals. 2014 Jun;27(3):601-7. doi: 10.1007/s10534-014-9733-8. Epub 2014 Apr 16.
5
The influence of biodegradable magnesium alloys on the osteogenic differentiation of human mesenchymal stem cells.可生物降解镁合金对人骨髓间充质干细胞成骨分化的影响。
J Biomed Mater Res A. 2014 Dec;102(12):4346-57. doi: 10.1002/jbm.a.35111. Epub 2014 Feb 24.
6
Magnesium ion stimulation of bone marrow stromal cells enhances osteogenic activity, simulating the effect of magnesium alloy degradation.镁离子刺激骨髓基质细胞增强成骨活性,模拟镁合金降解的作用。
Acta Biomater. 2014 Jun;10(6):2834-42. doi: 10.1016/j.actbio.2014.02.002. Epub 2014 Feb 7.
7
Effect of magnesium and calcium phosphate coatings on osteoblastic responses to the titanium surface.镁和磷酸钙涂层对钛表面成骨细胞反应的影响。
J Adv Prosthodont. 2013 Nov;5(4):402-8. doi: 10.4047/jap.2013.5.4.402. Epub 2013 Nov 28.
8
A novel strontium(II)-modified calcium phosphate bone cement stimulates human-bone-marrow-derived mesenchymal stem cell proliferation and osteogenic differentiation in vitro.一种新型锶(II)修饰的磷酸钙骨水泥在体外刺激人骨髓间充质干细胞的增殖和成骨分化。
Acta Biomater. 2013 Dec;9(12):9547-57. doi: 10.1016/j.actbio.2013.07.027. Epub 2013 Jul 31.
9
Accelerated bone ingrowth by local delivery of strontium from surface functionalized titanium implants.表面功能化钛植入物局部递送锶促进骨长入。
Biomaterials. 2013 Aug;34(24):5883-90. doi: 10.1016/j.biomaterials.2013.04.031. Epub 2013 May 11.
10
Bone integration capability of a series of strontium-containing hydroxyapatite coatings formed by micro-arc oxidation.微弧氧化形成的一系列含锶羟基磷灰石涂层的骨整合能力。
J Biomed Mater Res A. 2013 Sep;101(9):2465-80. doi: 10.1002/jbm.a.34548. Epub 2013 Jan 24.