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Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells

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 ch...

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Autores principales: Lin, Hengzhang, Zhou, Yong, Lei, Qun, Lin, Dong, Chen, Jiang, Wu, Chuhuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788862/
https://www.ncbi.nlm.nih.gov/pubmed/33407089
http://dx.doi.org/10.1186/s12861-020-00229-x
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author Lin, Hengzhang
Zhou, Yong
Lei, Qun
Lin, Dong
Chen, Jiang
Wu, Chuhuo
author_facet Lin, Hengzhang
Zhou, Yong
Lei, Qun
Lin, Dong
Chen, Jiang
Wu, Chuhuo
author_sort Lin, Hengzhang
collection PubMed
description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12861-020-00229-x.
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spelling pubmed-77888622021-01-07 Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells Lin, Hengzhang Zhou, Yong Lei, Qun Lin, Dong Chen, Jiang Wu, Chuhuo BMC Dev Biol Research Article 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12861-020-00229-x. BioMed Central 2021-01-06 /pmc/articles/PMC7788862/ /pubmed/33407089 http://dx.doi.org/10.1186/s12861-020-00229-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Lin, Hengzhang
Zhou, Yong
Lei, Qun
Lin, Dong
Chen, Jiang
Wu, Chuhuo
Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
title Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
title_full Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
title_fullStr Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
title_full_unstemmed Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
title_short Effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
title_sort effect of inorganic phosphate on migration and osteogenic differentiation of bone marrow mesenchymal stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788862/
https://www.ncbi.nlm.nih.gov/pubmed/33407089
http://dx.doi.org/10.1186/s12861-020-00229-x
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