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Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells

INTRODUCTION: Bisphosphonates (BPs) can be locally used to improve the osteogenesis around hydroxyapatite (HA) implants. However, there are almost no reports discussing the effects of BPs in the bonding state with HA on bone mesenchymal stromal cells (BMSCs). Clodronate is a BP widely used in clinic...

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Autores principales: Liu, Xian, Bao, Chongyun, Hu, Jing, Yin, Guozhu, Luo, En
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298333/
https://www.ncbi.nlm.nih.gov/pubmed/22419923
http://dx.doi.org/10.5114/aoms.2010.17079
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author Liu, Xian
Bao, Chongyun
Hu, Jing
Yin, Guozhu
Luo, En
author_facet Liu, Xian
Bao, Chongyun
Hu, Jing
Yin, Guozhu
Luo, En
author_sort Liu, Xian
collection PubMed
description INTRODUCTION: Bisphosphonates (BPs) can be locally used to improve the osteogenesis around hydroxyapatite (HA) implants. However, there are almost no reports discussing the effects of BPs in the bonding state with HA on bone mesenchymal stromal cells (BMSCs). Clodronate is a BP widely used in clinical practice. This study was designed to evaluate the effects of clodronate combined with HA on BMSCs’ multi-directional differentiation. MATERIAL AND METHODS: The HA and clodronate-HA complex were prepared. BMSCs were isolated from Sprague-Dawley rat bone marrow and then the cells were cultured with both HA and clodronate-HA. The method of transcriptional and translational assay (MTT) and multi-directional induction (including osteogenic, adipogenic, and myogenic differentiation) were used to evaluate the effect of clodronate-HA on BMSC differentiation. RESULTS: Scanning electron microscopy indicated active proliferation of the cells on clodronate-HA and HA. MTT of BMSCs cultured on clodronate-HA and HA demonstrated no significant differences between the two groups. BMSCs differentiated into osteocytes, adipocytes, and myocytes after being cultured with both clodronate-HA and HA. This indicated that BMSCs still retained multi-directional capability. The alkaline phosphatase activity of osteogenic induced BMSCs of both groups had no significant difference. However, there was a significant difference in total protein found between them. CONCLUSIONS: The results suggest that clodronate in the bonding state with HA has no obvious inhibition of the proliferation and activity of BMSCs on the complex, and there was no evidence of a negative effect on multi-directional capability of the BMSCs.
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spelling pubmed-32983332012-03-14 Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells Liu, Xian Bao, Chongyun Hu, Jing Yin, Guozhu Luo, En Arch Med Sci Basic Research INTRODUCTION: Bisphosphonates (BPs) can be locally used to improve the osteogenesis around hydroxyapatite (HA) implants. However, there are almost no reports discussing the effects of BPs in the bonding state with HA on bone mesenchymal stromal cells (BMSCs). Clodronate is a BP widely used in clinical practice. This study was designed to evaluate the effects of clodronate combined with HA on BMSCs’ multi-directional differentiation. MATERIAL AND METHODS: The HA and clodronate-HA complex were prepared. BMSCs were isolated from Sprague-Dawley rat bone marrow and then the cells were cultured with both HA and clodronate-HA. The method of transcriptional and translational assay (MTT) and multi-directional induction (including osteogenic, adipogenic, and myogenic differentiation) were used to evaluate the effect of clodronate-HA on BMSC differentiation. RESULTS: Scanning electron microscopy indicated active proliferation of the cells on clodronate-HA and HA. MTT of BMSCs cultured on clodronate-HA and HA demonstrated no significant differences between the two groups. BMSCs differentiated into osteocytes, adipocytes, and myocytes after being cultured with both clodronate-HA and HA. This indicated that BMSCs still retained multi-directional capability. The alkaline phosphatase activity of osteogenic induced BMSCs of both groups had no significant difference. However, there was a significant difference in total protein found between them. CONCLUSIONS: The results suggest that clodronate in the bonding state with HA has no obvious inhibition of the proliferation and activity of BMSCs on the complex, and there was no evidence of a negative effect on multi-directional capability of the BMSCs. Termedia Publishing House 2010-10-26 2010-10 /pmc/articles/PMC3298333/ /pubmed/22419923 http://dx.doi.org/10.5114/aoms.2010.17079 Text en Copyright © 2010 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Liu, Xian
Bao, Chongyun
Hu, Jing
Yin, Guozhu
Luo, En
Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
title Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
title_full Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
title_fullStr Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
title_full_unstemmed Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
title_short Effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
title_sort effects of clodronate combined with hydroxyapatite on multi-directional differentiation of mesenchymal stromal cells
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298333/
https://www.ncbi.nlm.nih.gov/pubmed/22419923
http://dx.doi.org/10.5114/aoms.2010.17079
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