Effect of magnesium on the osteogenesis of normal human osteoblasts.

IF 1.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wei-Chen Lu, Ekaterini Pringa, Laisheng Chou
{"title":"Effect of magnesium on the osteogenesis of normal human osteoblasts.","authors":"Wei-Chen Lu,&nbsp;Ekaterini Pringa,&nbsp;Laisheng Chou","doi":"10.1684/mrh.2017.0422","DOIUrl":null,"url":null,"abstract":"<p><p>Biomaterials containing magnesium are used for implants and bone regeneration. However, mechanisms underlying the biologic effects of magnesium are still largely unknown and have not been examined on normal human osteoblasts. This study was designed to test the effect of supplemented Mg<sup>2+</sup> concentrations between 0.5 mM and 16 mM on the osteogenic behaviors of normal human primary osteoblasts. Human primary osteoblasts were cultured in the groups with various concentrations of supplemented magnesium for various time intervals. Cell proliferation was measured using crystal violet staining. Degree of Alkaline Phosphatase (ALP) activity was measured by fluorometric assay. Expression of osteocalcin was measured by immunosorbent assay. Mineralization of cultures was determined by Alizarin Red S staining. Results showed that initial cell attachment efficiency was not affected by supplemented Mg<sup>2+</sup> (P > 0.05). At 21 days, proliferation rates increased in groups containing 0.5 mM-4 mM supplemented Mg<sup>2+</sup> and decreased in groups of supplemented 8 mM and 16 mM Mg<sup>2+</sup>. ALP activity and osteocalcin expression were upregulated in groups of supplemented Mg<sup>2+</sup> between 0.5 mM-2.0 mM (P < 0.05), but downregulated in groups with supplemented Mg<sup>2+</sup> concentrations of 4mM and above (P < 0.05). Cultures with 1 mM and 2 mM supplemented Mg<sup>2+</sup> showed upregulated mineralization activity compared to the control (P < 0.05), but downregulated in groups with supplemented Mg<sup>2+</sup> concentrations of 4 mM and above (P < 0.05). The present study based on an experimental design demonstrated the impact of 2 mM supplemented Mg<sup>2+</sup> on induced-proliferation and differentiation of normal human osteoblasts.</p>","PeriodicalId":18159,"journal":{"name":"Magnesium research","volume":"30 2","pages":"42-52"},"PeriodicalIF":1.5000,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1684/mrh.2017.0422","citationCount":"37","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Magnesium research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1684/mrh.2017.0422","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 37

Abstract

Biomaterials containing magnesium are used for implants and bone regeneration. However, mechanisms underlying the biologic effects of magnesium are still largely unknown and have not been examined on normal human osteoblasts. This study was designed to test the effect of supplemented Mg2+ concentrations between 0.5 mM and 16 mM on the osteogenic behaviors of normal human primary osteoblasts. Human primary osteoblasts were cultured in the groups with various concentrations of supplemented magnesium for various time intervals. Cell proliferation was measured using crystal violet staining. Degree of Alkaline Phosphatase (ALP) activity was measured by fluorometric assay. Expression of osteocalcin was measured by immunosorbent assay. Mineralization of cultures was determined by Alizarin Red S staining. Results showed that initial cell attachment efficiency was not affected by supplemented Mg2+ (P > 0.05). At 21 days, proliferation rates increased in groups containing 0.5 mM-4 mM supplemented Mg2+ and decreased in groups of supplemented 8 mM and 16 mM Mg2+. ALP activity and osteocalcin expression were upregulated in groups of supplemented Mg2+ between 0.5 mM-2.0 mM (P < 0.05), but downregulated in groups with supplemented Mg2+ concentrations of 4mM and above (P < 0.05). Cultures with 1 mM and 2 mM supplemented Mg2+ showed upregulated mineralization activity compared to the control (P < 0.05), but downregulated in groups with supplemented Mg2+ concentrations of 4 mM and above (P < 0.05). The present study based on an experimental design demonstrated the impact of 2 mM supplemented Mg2+ on induced-proliferation and differentiation of normal human osteoblasts.

镁对正常人成骨细胞成骨的影响。
含镁的生物材料用于植入物和骨再生。然而,镁的生物学作用机制在很大程度上仍然是未知的,并且尚未在正常的人类成骨细胞中进行检测。本研究旨在检测0.5 mM ~ 16 mM浓度的Mg2+对正常人原代成骨细胞成骨行为的影响。在不同的补镁浓度、不同的时间间隔组中培养人原代成骨细胞。结晶紫染色测定细胞增殖。用荧光法测定碱性磷酸酶(ALP)活性。免疫吸附法检测骨钙素的表达。用茜素红S染色法测定培养物的矿化程度。结果表明,Mg2+对细胞初始附着效率无显著影响(P > 0.05)。21 d时,0.5 mM-4 mM Mg2+组增殖率升高,8 mM和16 mM Mg2+组增殖率降低。在0.5 mM-2.0 mM范围内,添加Mg2+组ALP活性和骨钙素表达上调(pg2 +浓度为4mM及以上)(与对照组(pg2 +浓度为4mM及以上)(pg2 +矿化活性上调)(pg2 +诱导正常人成骨细胞增殖和分化)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Magnesium research
Magnesium research 医学-内分泌学与代谢
CiteScore
3.50
自引率
9.40%
发文量
6
审稿时长
>12 weeks
期刊介绍: Magnesium Research, the official journal of the international Society for the Development of Research on Magnesium (SDRM), has been the benchmark journal on the use of magnesium in biomedicine for more than 30 years. This quarterly publication provides regular updates on multinational and multidisciplinary research into magnesium, bringing together original experimental and clinical articles, correspondence, Letters to the Editor, comments on latest news, general features, summaries of relevant articles from other journals, and reports and statements from national and international conferences and symposiums. Indexed in the leading medical databases, Magnesium Research is an essential journal for specialists and general practitioners, for basic and clinical researchers, for practising doctors and academics.
×
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