{"title":"Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells.","authors":"Hengzhang Lin, Yong Zhou, Qun Lei, Dong Lin, Jiang Chen, Chuhuo Wu","doi":"10.1186/s12861-020-00229-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Phosphate is the major ingredient of bone tissue, and is also an important component of commercial bone substitute materials, bone scaffolds, and implant surface coatings. With the dissolution of the bone substitute materials and the degradation by cells, local ion concentrations will change and affect bone tissue reconstruction. Bone marrow -derived mesenchymal stem cells (BM-MSCs) are main autologous cells to repair injured bone. When bone injure occurs, BM-MSCs migrate to the damaged area, differentiate into osteoblasts, and secrete bioactive factors to promote bone tissue repaired. This study aimed to investigate the effect of inorganic phosphate (Pi) at a series of concentration on migration and osteogenic differentiation of human bone marrow -derived mesenchymal stem cells(hBM-MSCs).</p><p><strong>Methods: </strong>The culture of hBM-MSCs in mediums with different concentration of Pi from 2 mM to 10 mM were performed. HBM-MSCs migration were examined with transwell assays. HBM-MSCs proliferation were evaluated by cell counting kit-8 colorimetric method. Osteogenic genes expression were analyzed by real-time reverse transcriptase polymerase chain reaction. Mineralized nodules formation were demonstrated by Alizarin red staining.</p><p><strong>Result: </strong>4-10 mM Pi could effectively promote the migration of hBM-MSCs at 12 h and 18 h. There was no significant difference in the migration number of hBM-MSCs in Pi culture mediums at a concentration of 6, 8, and10mM. 2-10 mM Pi could promote the proliferation of hBM-MSCs to varying degrees in the observation period, while 4-10 mM Pi could promote the osteogenic differentiation and mineralization of hBM-MSCs.</p><p><strong>Conclusion: </strong>The findings in our study showed 4-10 mM Pi could promote the migration, osteogenic differentiation, and mineralization of hBM-MSCs.</p>","PeriodicalId":9130,"journal":{"name":"BMC Developmental Biology","volume":" ","pages":"1"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788862/pdf/","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Developmental Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12861-020-00229-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 10
Abstract
Background: Phosphate is the major ingredient of bone tissue, and is also an important component of commercial bone substitute materials, bone scaffolds, and implant surface coatings. With the dissolution of the bone substitute materials and the degradation by cells, local ion concentrations will change and affect bone tissue reconstruction. Bone marrow -derived mesenchymal stem cells (BM-MSCs) are main autologous cells to repair injured bone. When bone injure occurs, BM-MSCs migrate to the damaged area, differentiate into osteoblasts, and secrete bioactive factors to promote bone tissue repaired. This study aimed to investigate the effect of inorganic phosphate (Pi) at a series of concentration on migration and osteogenic differentiation of human bone marrow -derived mesenchymal stem cells(hBM-MSCs).
Methods: The culture of hBM-MSCs in mediums with different concentration of Pi from 2 mM to 10 mM were performed. HBM-MSCs migration were examined with transwell assays. HBM-MSCs proliferation were evaluated by cell counting kit-8 colorimetric method. Osteogenic genes expression were analyzed by real-time reverse transcriptase polymerase chain reaction. Mineralized nodules formation were demonstrated by Alizarin red staining.
Result: 4-10 mM Pi could effectively promote the migration of hBM-MSCs at 12 h and 18 h. There was no significant difference in the migration number of hBM-MSCs in Pi culture mediums at a concentration of 6, 8, and10mM. 2-10 mM Pi could promote the proliferation of hBM-MSCs to varying degrees in the observation period, while 4-10 mM Pi could promote the osteogenic differentiation and mineralization of hBM-MSCs.
Conclusion: The findings in our study showed 4-10 mM Pi could promote the migration, osteogenic differentiation, and mineralization of hBM-MSCs.
背景:磷酸盐是骨组织的主要成分,也是商用骨替代材料、骨支架和种植体表面涂层的重要成分。随着骨替代材料的溶解和细胞的降解,局部离子浓度会发生变化,影响骨组织重建。骨髓间充质干细胞(bmscs)是修复骨损伤的主要自体细胞。骨损伤发生后,BM-MSCs向损伤部位迁移,分化为成骨细胞,并分泌生物活性因子促进骨组织修复。本研究旨在探讨不同浓度的无机磷酸盐(Pi)对人骨髓间充质干细胞(hBM-MSCs)迁移和成骨分化的影响。方法:在2 ~ 10 mM不同浓度Pi的培养基中培养hBM-MSCs。用transwell法检测HBM-MSCs迁移。采用细胞计数试剂盒-8比色法检测HBM-MSCs的增殖情况。实时逆转录聚合酶链反应分析成骨基因表达。茜素红染色显示矿化结节形成。结果:4 ~ 10 mM Pi能有效促进hBM-MSCs在12 h和18 h的迁移。在浓度为6、8和10mm的Pi培养基中,hBM-MSCs的迁移数量没有显著差异。观察期内,2-10 mM Pi可不同程度促进hBM-MSCs的增殖,4-10 mM Pi可促进hBM-MSCs的成骨分化和矿化。结论:4 ~ 10 mM Pi能促进hBM-MSCs的迁移、成骨分化和矿化。
期刊介绍:
BMC Developmental Biology is an open access, peer-reviewed journal that considers articles on the development, growth, differentiation and regeneration of multicellular organisms, including molecular, cellular, tissue, organ and whole organism research.