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The polymine spermine regulates osteogenic differentiation in adipose stem cells

For bone tissue engineering, it is important that mesenchymal stem cells (MSCs) differentiate into osteoblasts. To develop a method for differentiation of adipose tissue-derived mesenchymal stem cells (AT-MSCs) along the osteogenic lineage, we studied the effect of polyamines, which are organic cati...

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Autores principales: Tjabringa, GS, Zandieh-Doulabi, B, Helder, MN, Knippenberg, M, Wuisman, PIJM, Klein-Nulend, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918087/
https://www.ncbi.nlm.nih.gov/pubmed/18194460
http://dx.doi.org/10.1111/j.1582-4934.2008.00224.x
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author Tjabringa, GS
Zandieh-Doulabi, B
Helder, MN
Knippenberg, M
Wuisman, PIJM
Klein-Nulend, J
author_facet Tjabringa, GS
Zandieh-Doulabi, B
Helder, MN
Knippenberg, M
Wuisman, PIJM
Klein-Nulend, J
author_sort Tjabringa, GS
collection PubMed
description For bone tissue engineering, it is important that mesenchymal stem cells (MSCs) differentiate into osteoblasts. To develop a method for differentiation of adipose tissue-derived mesenchymal stem cells (AT-MSCs) along the osteogenic lineage, we studied the effect of polyamines, which are organic cations implicated in bone growth and development, on differentiation of AT-MSCs. Treatment of goat-derived AT-MSCs with 1,25-dihydroxyvitamin-D3 (1,25(OH)(2)D(3)), which stimulates osteogenic differentiation, for 7 days induced gene expression of the polyamine-modulated transcription factor-1 (PMF-1) and spermidine/spermine N (1)-acetyltransferase (SSAT), which are both involved in polyamine metabolism, suggesting that polyamines are involved in osteogenic differentiation of AT-MSCs. Furthermore, treatment of AT-MSCs with the polyamine spermine-regulated gene expression of runx-2, a transcription factor involved in early stages of osteogenic differentiation, and that of osteopontin, a bone matrix protein expressed in later stages of osteogenic differentiation. Runx-2 gene expression was increased 4 and 14 days after a short 30 min. treatment with spermine, while osteopontin gene expression was only increased 4 days after spermine treatment. Finally, alkaline phosphatase activity, which is intimately involved in the formation of extracellular matrix of bone, was increased 4 weeks after the 30 min.-spermine treatment of AT-MSCs. In conclusion, this study shows for the first time that the polyamine spermine regulates differentiation of AT-MSCs along the osteogenic lineage, which can be used as a new method for differentiation of AT-MSCs along the osteogenic lineage. Therefore, polyamines may constitute a promising tool for bone tissue engineering approaches using AT-MSCs, such as a one-step surgical procedure for spinal interbody fusion.
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spelling pubmed-39180872015-04-27 The polymine spermine regulates osteogenic differentiation in adipose stem cells Tjabringa, GS Zandieh-Doulabi, B Helder, MN Knippenberg, M Wuisman, PIJM Klein-Nulend, J J Cell Mol Med Articles For bone tissue engineering, it is important that mesenchymal stem cells (MSCs) differentiate into osteoblasts. To develop a method for differentiation of adipose tissue-derived mesenchymal stem cells (AT-MSCs) along the osteogenic lineage, we studied the effect of polyamines, which are organic cations implicated in bone growth and development, on differentiation of AT-MSCs. Treatment of goat-derived AT-MSCs with 1,25-dihydroxyvitamin-D3 (1,25(OH)(2)D(3)), which stimulates osteogenic differentiation, for 7 days induced gene expression of the polyamine-modulated transcription factor-1 (PMF-1) and spermidine/spermine N (1)-acetyltransferase (SSAT), which are both involved in polyamine metabolism, suggesting that polyamines are involved in osteogenic differentiation of AT-MSCs. Furthermore, treatment of AT-MSCs with the polyamine spermine-regulated gene expression of runx-2, a transcription factor involved in early stages of osteogenic differentiation, and that of osteopontin, a bone matrix protein expressed in later stages of osteogenic differentiation. Runx-2 gene expression was increased 4 and 14 days after a short 30 min. treatment with spermine, while osteopontin gene expression was only increased 4 days after spermine treatment. Finally, alkaline phosphatase activity, which is intimately involved in the formation of extracellular matrix of bone, was increased 4 weeks after the 30 min.-spermine treatment of AT-MSCs. In conclusion, this study shows for the first time that the polyamine spermine regulates differentiation of AT-MSCs along the osteogenic lineage, which can be used as a new method for differentiation of AT-MSCs along the osteogenic lineage. Therefore, polyamines may constitute a promising tool for bone tissue engineering approaches using AT-MSCs, such as a one-step surgical procedure for spinal interbody fusion. Blackwell Publishing Ltd 2008-09 2008-01-11 /pmc/articles/PMC3918087/ /pubmed/18194460 http://dx.doi.org/10.1111/j.1582-4934.2008.00224.x Text en © 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Tjabringa, GS
Zandieh-Doulabi, B
Helder, MN
Knippenberg, M
Wuisman, PIJM
Klein-Nulend, J
The polymine spermine regulates osteogenic differentiation in adipose stem cells
title The polymine spermine regulates osteogenic differentiation in adipose stem cells
title_full The polymine spermine regulates osteogenic differentiation in adipose stem cells
title_fullStr The polymine spermine regulates osteogenic differentiation in adipose stem cells
title_full_unstemmed The polymine spermine regulates osteogenic differentiation in adipose stem cells
title_short The polymine spermine regulates osteogenic differentiation in adipose stem cells
title_sort polymine spermine regulates osteogenic differentiation in adipose stem cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918087/
https://www.ncbi.nlm.nih.gov/pubmed/18194460
http://dx.doi.org/10.1111/j.1582-4934.2008.00224.x
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