Cargando…
Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold
Combination of tissue engineering and cell therapy represents a promising approach for bone regeneration. Human mesenchymal stem cells (hMSCs) have properties that include low immunogenicity, high proliferation rate, and multi-differentiation potential; therefore, they are an attractive seeding sour...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879338/ https://www.ncbi.nlm.nih.gov/pubmed/24396384 http://dx.doi.org/10.5625/lar.2013.29.4.196 |
_version_ | 1782297965334888448 |
---|---|
author | Im, Jin-Young Min, Woo-Kie You, Changkook Kim, Hyun-Ok Jin, Hee-Kyung Bae, Jae-sung |
author_facet | Im, Jin-Young Min, Woo-Kie You, Changkook Kim, Hyun-Ok Jin, Hee-Kyung Bae, Jae-sung |
author_sort | Im, Jin-Young |
collection | PubMed |
description | Combination of tissue engineering and cell therapy represents a promising approach for bone regeneration. Human mesenchymal stem cells (hMSCs) have properties that include low immunogenicity, high proliferation rate, and multi-differentiation potential; therefore, they are an attractive seeding source for tissue engineering therapy. Here we found that hMSCs with a scaffold did not affect cell viability and osteogenic differentiation. We also investigated regenerative effect of hMSCs with the scaffold in a calvarial bone defect model. Formation of new bone was evaluated by micro-CT, histology and expression of osteogenic markers. The results clearly showed interesting evidence indicating that hMSCs with scaffold increased the formation of new bone and expression of osteogenic markers, compared to the empty and scaffold only groups. Overall, our results suggest that hMSCs with scaffold are suitable for stimulation of intense bone regeneration in critical-sized bone defects. |
format | Online Article Text |
id | pubmed-3879338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38793382014-01-06 Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold Im, Jin-Young Min, Woo-Kie You, Changkook Kim, Hyun-Ok Jin, Hee-Kyung Bae, Jae-sung Lab Anim Res Original Article Combination of tissue engineering and cell therapy represents a promising approach for bone regeneration. Human mesenchymal stem cells (hMSCs) have properties that include low immunogenicity, high proliferation rate, and multi-differentiation potential; therefore, they are an attractive seeding source for tissue engineering therapy. Here we found that hMSCs with a scaffold did not affect cell viability and osteogenic differentiation. We also investigated regenerative effect of hMSCs with the scaffold in a calvarial bone defect model. Formation of new bone was evaluated by micro-CT, histology and expression of osteogenic markers. The results clearly showed interesting evidence indicating that hMSCs with scaffold increased the formation of new bone and expression of osteogenic markers, compared to the empty and scaffold only groups. Overall, our results suggest that hMSCs with scaffold are suitable for stimulation of intense bone regeneration in critical-sized bone defects. Korean Association for Laboratory Animal Science 2013-12 2013-12-20 /pmc/articles/PMC3879338/ /pubmed/24396384 http://dx.doi.org/10.5625/lar.2013.29.4.196 Text en Copyright © 2013 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Im, Jin-Young Min, Woo-Kie You, Changkook Kim, Hyun-Ok Jin, Hee-Kyung Bae, Jae-sung Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
title | Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
title_full | Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
title_fullStr | Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
title_full_unstemmed | Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
title_short | Bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
title_sort | bone regeneration of mouse critical-sized calvarial defects with human mesenchymal stem cells in scaffold |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3879338/ https://www.ncbi.nlm.nih.gov/pubmed/24396384 http://dx.doi.org/10.5625/lar.2013.29.4.196 |
work_keys_str_mv | AT imjinyoung boneregenerationofmousecriticalsizedcalvarialdefectswithhumanmesenchymalstemcellsinscaffold AT minwookie boneregenerationofmousecriticalsizedcalvarialdefectswithhumanmesenchymalstemcellsinscaffold AT youchangkook boneregenerationofmousecriticalsizedcalvarialdefectswithhumanmesenchymalstemcellsinscaffold AT kimhyunok boneregenerationofmousecriticalsizedcalvarialdefectswithhumanmesenchymalstemcellsinscaffold AT jinheekyung boneregenerationofmousecriticalsizedcalvarialdefectswithhumanmesenchymalstemcellsinscaffold AT baejaesung boneregenerationofmousecriticalsizedcalvarialdefectswithhumanmesenchymalstemcellsinscaffold |