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Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro

OBEJECTIVE: To investigate the effect of increasing Strontium (Sr) concentrations on the growth and osteogenic behavior of human bone marrow stromal cells (BMSCs) from mesenchymal (i.e., fibula) and ectomesenchymal (i.e., mandible) embryonic origins. MATERIALS AND METHODS: Fibula and mandible BMSCs...

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Autores principales: Bizelli‐Silveira, Carolina, Abildtrup, Lisbeth Ann, Spin‐Neto, Rubens, Foss, Morten, Søballe, Kjeld, Kraft, David Christian Evar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820574/
https://www.ncbi.nlm.nih.gov/pubmed/31687189
http://dx.doi.org/10.1002/cre2.221
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author Bizelli‐Silveira, Carolina
Abildtrup, Lisbeth Ann
Spin‐Neto, Rubens
Foss, Morten
Søballe, Kjeld
Kraft, David Christian Evar
author_facet Bizelli‐Silveira, Carolina
Abildtrup, Lisbeth Ann
Spin‐Neto, Rubens
Foss, Morten
Søballe, Kjeld
Kraft, David Christian Evar
author_sort Bizelli‐Silveira, Carolina
collection PubMed
description OBEJECTIVE: To investigate the effect of increasing Strontium (Sr) concentrations on the growth and osteogenic behavior of human bone marrow stromal cells (BMSCs) from mesenchymal (i.e., fibula) and ectomesenchymal (i.e., mandible) embryonic origins. MATERIALS AND METHODS: Fibula and mandible BMSCs were cultured in media without (Ctrl) or with Sr in four diverse concentrations: Sr1, 11.3 × 10(−3) mg/L, human seric physiological level; Sr2, 13 mg/L, human seric level after strontium ranelate treatment; Sr3, 130 mg/L, and Sr4, 360 mg/L. Proliferation rate (1, 3, and 7 days), osteogenic behavior (alkaline phosphatase [ALP] activity, 7 and 14 days; expression of osteogenic genes (ALP, osteopontin, and osteocalcin at 7, 14, and 21 days), and formation of mineralized nodules (14 and 21 days) of the BMSCs were assessed. Data was compared group‐ and period‐wise using analysis of variance tests. RESULTS: Fibula and mandible BMSCs cultured with Sr4 showed increased proliferation rate, and osteocalcin and osteopontin gene expression together with more evident formation of mineralized nodules, compared all other Sr concentrations. For both cell populations, Sr4 led to lower ALP activity, and ALP gene expression, compared with the other Sr concentrations. CONCLUSION: BMSCs from mesenchymal (i.e., fibula) and ectomesenchymal (i.e., mandible) embryonic origins showed increased cellular proliferation and osteogenic behavior when cultured with Sr4, in vitro.
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spelling pubmed-68205742019-11-04 Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro Bizelli‐Silveira, Carolina Abildtrup, Lisbeth Ann Spin‐Neto, Rubens Foss, Morten Søballe, Kjeld Kraft, David Christian Evar Clin Exp Dent Res Original Articles OBEJECTIVE: To investigate the effect of increasing Strontium (Sr) concentrations on the growth and osteogenic behavior of human bone marrow stromal cells (BMSCs) from mesenchymal (i.e., fibula) and ectomesenchymal (i.e., mandible) embryonic origins. MATERIALS AND METHODS: Fibula and mandible BMSCs were cultured in media without (Ctrl) or with Sr in four diverse concentrations: Sr1, 11.3 × 10(−3) mg/L, human seric physiological level; Sr2, 13 mg/L, human seric level after strontium ranelate treatment; Sr3, 130 mg/L, and Sr4, 360 mg/L. Proliferation rate (1, 3, and 7 days), osteogenic behavior (alkaline phosphatase [ALP] activity, 7 and 14 days; expression of osteogenic genes (ALP, osteopontin, and osteocalcin at 7, 14, and 21 days), and formation of mineralized nodules (14 and 21 days) of the BMSCs were assessed. Data was compared group‐ and period‐wise using analysis of variance tests. RESULTS: Fibula and mandible BMSCs cultured with Sr4 showed increased proliferation rate, and osteocalcin and osteopontin gene expression together with more evident formation of mineralized nodules, compared all other Sr concentrations. For both cell populations, Sr4 led to lower ALP activity, and ALP gene expression, compared with the other Sr concentrations. CONCLUSION: BMSCs from mesenchymal (i.e., fibula) and ectomesenchymal (i.e., mandible) embryonic origins showed increased cellular proliferation and osteogenic behavior when cultured with Sr4, in vitro. John Wiley and Sons Inc. 2019-08-21 /pmc/articles/PMC6820574/ /pubmed/31687189 http://dx.doi.org/10.1002/cre2.221 Text en ©2019 The Authors. Clinical and Experimental Dental Research published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bizelli‐Silveira, Carolina
Abildtrup, Lisbeth Ann
Spin‐Neto, Rubens
Foss, Morten
Søballe, Kjeld
Kraft, David Christian Evar
Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
title Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
title_full Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
title_fullStr Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
title_full_unstemmed Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
title_short Strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
title_sort strontium enhances proliferation and osteogenic behavior of bone marrow stromal cells of mesenchymal and ectomesenchymal origins in vitro
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820574/
https://www.ncbi.nlm.nih.gov/pubmed/31687189
http://dx.doi.org/10.1002/cre2.221
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