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Early Effects of P-15 on Human Bone Marrow Stem Cells
OBJECTIVES: Peptide-15 (P-15) is an analogue of the cell binding domain of collagen. P-15 has been shown to facilitate physiological to process in a way similar to collagen, to serve as anchorage for cells, and to promote the binding, migration and differentiation of cells. However, how P-15 alters...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Stilus Optimus
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886042/ https://www.ncbi.nlm.nih.gov/pubmed/24421960 http://dx.doi.org/10.5037/jomr.2010.1104 |
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author | Sollazzo, Vincenzo Palmieri, Annalisa Girardi, Ambra Farinella, Francesca Carinci, Francesco |
author_facet | Sollazzo, Vincenzo Palmieri, Annalisa Girardi, Ambra Farinella, Francesca Carinci, Francesco |
author_sort | Sollazzo, Vincenzo |
collection | PubMed |
description | OBJECTIVES: Peptide-15 (P-15) is an analogue of the cell binding domain of collagen. P-15 has been shown to facilitate physiological to process in a way similar to collagen, to serve as anchorage for cells, and to promote the binding, migration and differentiation of cells. However, how P-15 alters osteoblast activity to promote bone formation is poorly understood. To study the osteoinductive properties of peptide P-15, we analyzed the expression levels of bone related genes in human mesenchymal stem cells treated with this biomaterial. MATERIAL AND METHODS: Using real time Reverse Transcription-Polymerase Chain Reaction the quantitative expression of specific genes, like transcriptional factors (RUNX2 and SP7), bone related genes (SPP1, COL1A1, COL3A1, BGLAP, ALPL, and FOSL1) and mesenchymal stem cells marker (ENG) were examined. RESULTS: P-15 causes a considerable induction of osteoblast transcriptional factor like osterix (SP7) and of the bone related genes osteopontin (SPP1) and osteocalcin (BGLAP). In contrast the expression of endoglin (ENG) was markedly decreased in stem cells treated with P-15 respect to untreated cells, indicating the differentiation effect of this biomaterial on stem cells. CONCLUSIONS: The present study shows the effect of P-15 on mesenchymal stem cells in the early differentiation stages: P-15 is an inducer of osteogenesis on human stem cells as indicated by the activation of bone related markers SP7, SPP1 and BGLAP.The results may allow a better understanding of the molecular mechanism of bone regeneration and as a model for comparing other materials with similar clinical effects. |
format | Online Article Text |
id | pubmed-3886042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Stilus Optimus |
record_format | MEDLINE/PubMed |
spelling | pubmed-38860422014-01-13 Early Effects of P-15 on Human Bone Marrow Stem Cells Sollazzo, Vincenzo Palmieri, Annalisa Girardi, Ambra Farinella, Francesca Carinci, Francesco J Oral Maxillofac Res Original Paper OBJECTIVES: Peptide-15 (P-15) is an analogue of the cell binding domain of collagen. P-15 has been shown to facilitate physiological to process in a way similar to collagen, to serve as anchorage for cells, and to promote the binding, migration and differentiation of cells. However, how P-15 alters osteoblast activity to promote bone formation is poorly understood. To study the osteoinductive properties of peptide P-15, we analyzed the expression levels of bone related genes in human mesenchymal stem cells treated with this biomaterial. MATERIAL AND METHODS: Using real time Reverse Transcription-Polymerase Chain Reaction the quantitative expression of specific genes, like transcriptional factors (RUNX2 and SP7), bone related genes (SPP1, COL1A1, COL3A1, BGLAP, ALPL, and FOSL1) and mesenchymal stem cells marker (ENG) were examined. RESULTS: P-15 causes a considerable induction of osteoblast transcriptional factor like osterix (SP7) and of the bone related genes osteopontin (SPP1) and osteocalcin (BGLAP). In contrast the expression of endoglin (ENG) was markedly decreased in stem cells treated with P-15 respect to untreated cells, indicating the differentiation effect of this biomaterial on stem cells. CONCLUSIONS: The present study shows the effect of P-15 on mesenchymal stem cells in the early differentiation stages: P-15 is an inducer of osteogenesis on human stem cells as indicated by the activation of bone related markers SP7, SPP1 and BGLAP.The results may allow a better understanding of the molecular mechanism of bone regeneration and as a model for comparing other materials with similar clinical effects. Stilus Optimus 2010-04-01 /pmc/articles/PMC3886042/ /pubmed/24421960 http://dx.doi.org/10.5037/jomr.2010.1104 Text en Copyright © Sollazzo V, Palmieri A, Girardi A, Farinella F, Carinci F. Published in the JOURNAL OF ORAL & MAXILLOFACIAL RESEARCH (http://www.ejomr.org), 1 April 2010. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article, first published in the JOURNAL OF ORAL & MAXILLOFACIAL RESEARCH, distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work and is properly cited. The copyright, license information and link to the original publication on http://www.ejomr.org must be included. |
spellingShingle | Original Paper Sollazzo, Vincenzo Palmieri, Annalisa Girardi, Ambra Farinella, Francesca Carinci, Francesco Early Effects of P-15 on Human Bone Marrow Stem Cells |
title | Early Effects of P-15 on Human Bone Marrow Stem Cells |
title_full | Early Effects of P-15 on Human Bone Marrow Stem Cells |
title_fullStr | Early Effects of P-15 on Human Bone Marrow Stem Cells |
title_full_unstemmed | Early Effects of P-15 on Human Bone Marrow Stem Cells |
title_short | Early Effects of P-15 on Human Bone Marrow Stem Cells |
title_sort | early effects of p-15 on human bone marrow stem cells |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886042/ https://www.ncbi.nlm.nih.gov/pubmed/24421960 http://dx.doi.org/10.5037/jomr.2010.1104 |
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