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In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes

OBJECTIVE(S): Tissue engineering is an attractive science because it promises new therapeutic strategies for repairing organs that have lost functions due to damage. The purpose of this study was to evaluate induction effect of human gingival scaffold in tissue engineering for skin regeneration. MAT...

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Autores principales: Mahdavishahri, Nasser, Moghatam Matin, Maryam, Fereidoni, Masoud, Yarjanli, Zahra, Banihashem Rad, Seyed Ali, Khajeh Ahmadi, Saeedeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646230/
https://www.ncbi.nlm.nih.gov/pubmed/23653849
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author Mahdavishahri, Nasser
Moghatam Matin, Maryam
Fereidoni, Masoud
Yarjanli, Zahra
Banihashem Rad, Seyed Ali
Khajeh Ahmadi, Saeedeh
author_facet Mahdavishahri, Nasser
Moghatam Matin, Maryam
Fereidoni, Masoud
Yarjanli, Zahra
Banihashem Rad, Seyed Ali
Khajeh Ahmadi, Saeedeh
author_sort Mahdavishahri, Nasser
collection PubMed
description OBJECTIVE(S): Tissue engineering is an attractive science because it promises new therapeutic strategies for repairing organs that have lost functions due to damage. The purpose of this study was to evaluate induction effect of human gingival scaffold in tissue engineering for skin regeneration. MATERIALS AND METHODS: Tissue samples were obtained from crown-lengthening procedures and wisdom teeth removal. The samples were decellularized and used as a scaffold for loading of rat BM-MSCs. The human gingival scaffolds loaded by bone marrow mesenchymal stem cells were derived from Wistar rat. Finally, it was evaluated via electron micrographs, as well as immunohistochemical techniques at day 7, 14, and 28 after initial seeding. RESULTS: The histologic sections of human gingival scaffold –loaded rat BM-MSCs demonstrated formation of epithelial like layers at days 7, 14 and 28 after initial seeding. Scanning electron microscope (SEM) of the scaffolds indicated formed desmosomal adhesions, which revealed a degree of differentiation toward keratinocytes. The results of immunohistochemical staining were strongly positive for multi cytokeratin (CK) 14 days after initial seeding in epithelial differentiation. Rat BM-MSCs which loaded on human gingival scaffold is capable of differentiating toward keratinocytes. CONCLUSION: Gingival tissues were presented as a natural scaffold for attachment and differentiation of bone marrow mesenchymal stem cells towards keratinocytes, and might be used as suitable scaffold for reconstruction of the skin.
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spelling pubmed-36462302013-05-07 In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes Mahdavishahri, Nasser Moghatam Matin, Maryam Fereidoni, Masoud Yarjanli, Zahra Banihashem Rad, Seyed Ali Khajeh Ahmadi, Saeedeh Iran J Basic Med Sci Original Article OBJECTIVE(S): Tissue engineering is an attractive science because it promises new therapeutic strategies for repairing organs that have lost functions due to damage. The purpose of this study was to evaluate induction effect of human gingival scaffold in tissue engineering for skin regeneration. MATERIALS AND METHODS: Tissue samples were obtained from crown-lengthening procedures and wisdom teeth removal. The samples were decellularized and used as a scaffold for loading of rat BM-MSCs. The human gingival scaffolds loaded by bone marrow mesenchymal stem cells were derived from Wistar rat. Finally, it was evaluated via electron micrographs, as well as immunohistochemical techniques at day 7, 14, and 28 after initial seeding. RESULTS: The histologic sections of human gingival scaffold –loaded rat BM-MSCs demonstrated formation of epithelial like layers at days 7, 14 and 28 after initial seeding. Scanning electron microscope (SEM) of the scaffolds indicated formed desmosomal adhesions, which revealed a degree of differentiation toward keratinocytes. The results of immunohistochemical staining were strongly positive for multi cytokeratin (CK) 14 days after initial seeding in epithelial differentiation. Rat BM-MSCs which loaded on human gingival scaffold is capable of differentiating toward keratinocytes. CONCLUSION: Gingival tissues were presented as a natural scaffold for attachment and differentiation of bone marrow mesenchymal stem cells towards keratinocytes, and might be used as suitable scaffold for reconstruction of the skin. Mashhad University of Medical Sciences 2012 /pmc/articles/PMC3646230/ /pubmed/23653849 Text en © 2012: Iranian Journal of Basic Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mahdavishahri, Nasser
Moghatam Matin, Maryam
Fereidoni, Masoud
Yarjanli, Zahra
Banihashem Rad, Seyed Ali
Khajeh Ahmadi, Saeedeh
In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes
title In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes
title_full In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes
title_fullStr In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes
title_full_unstemmed In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes
title_short In vitro Assay of Human Gingival Scaffold in Differentiation of Rat’s Bone Marrow Mesenchymal Stem Cells to Keratinocystes
title_sort in vitro assay of human gingival scaffold in differentiation of rat’s bone marrow mesenchymal stem cells to keratinocystes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646230/
https://www.ncbi.nlm.nih.gov/pubmed/23653849
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