Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect
Mesenchymal stem cells sheets have been verified as a promising non-scaffold strategy for bone regeneration. Alveolar bone marrow mesenchymal stem cells, derived from neural crest, have the character of easily obtained and strong multi-differential potential. However, the bone regenerative features...
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doaj-e502b24a35ef4afb85b7c8e266c6951d2020-11-25T03:20:49ZengSAGE PublishingJournal of Tissue Engineering2041-73142020-06-011110.1177/2041731420930379Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defectYanan Liu0Haifeng Wang1Huixin Dou2Bin Tian3Le Li4Luyuan Jin5Zhenting Zhang6Lei Hu7Department of Prosthodontics, School of Stomatology, Capital Medical University, Beijing, ChinaDepartment of Stomatology, Beijing Bo’ai Hospital, China Rehabilitation Research Center, School of Rehabilitation, Capital Medical University, Beijing, ChinaBeijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, Beijing, ChinaDepartment of Prosthodontics, School of Stomatology, Capital Medical University, Beijing, ChinaDepartment of Stomatology, Tsinghua University Hospital, Beijing, ChinaBeijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, Beijing, ChinaDepartment of Prosthodontics, School of Stomatology, Capital Medical University, Beijing, ChinaDepartment of Prosthodontics, School of Stomatology, Capital Medical University, Beijing, ChinaMesenchymal stem cells sheets have been verified as a promising non-scaffold strategy for bone regeneration. Alveolar bone marrow mesenchymal stem cells, derived from neural crest, have the character of easily obtained and strong multi-differential potential. However, the bone regenerative features of alveolar bone marrow mesenchymal stem cells sheets in the craniofacial region remain unclear. The purpose of the present study was to compare the osteogenic differentiation and bone defect repairment characteristics of bone marrow mesenchymal stem cells sheets derived from alveolar bone (alveolar bone marrow mesenchymal stem cells) and iliac bone (Lon-bone marrow mesenchymal stem cells) in vitro and in vivo . Histology character, osteogenic differentiation, and osteogenic gene expression of human alveolar bone marrow mesenchymal stem cells and Lon-bone marrow mesenchymal stem cells were compared in vitro . The cell sheets were implanted in rabbit calvarial defects to evaluate tissue regeneration characteristics. Integrated bioinformatics analysis was used to reveal the specific gene and pathways expression profile of alveolar bone marrow mesenchymal stem cells. Our results showed that alveolar bone marrow mesenchymal stem cells had higher osteogenic differentiation than Lon-bone marrow mesenchymal stem cells. Although no obvious differences were found in the histological structure, fibronectin and integrin β1 expression between them, alveolar-bone marrow mesenchymal stem cells sheet exhibited higher mineral deposition and expression levels of osteogenic marker genes. After being transplanted in the rabbit calvarial defects area, the results showed that greater bone volume and trabecular thickness regeneration were found in bone marrow mesenchymal stem cells sheet group compared to Lon-bone marrow mesenchymal stem cells group at both 4 weeks and 8 weeks. Finally, datasets of bone marrow mesenchymal stem cells versus Lon-bone marrow mesenchymal stem cells, and periodontal ligament mesenchymal stem cells (another neural crest derived mesenchymal stem cells) versus umbilical cord mesenchymal stem cells were analyzed. Total 71 differential genes were identified by overlap between the 2 datasets. Homeobox genes, such as LHX8, MKX, PAX9, MSX , and HOX , were identified as the most significantly changed and would be potential specific genes in neural crest mesenchymal stem cells. In conclusion, the Al-bone marrow mesenchymal stem cells sheet-based tissue regeneration appears to be a promising strategy for craniofacial defect repair in future clinical applications.https://doi.org/10.1177/2041731420930379 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yanan Liu Haifeng Wang Huixin Dou Bin Tian Le Li Luyuan Jin Zhenting Zhang Lei Hu |
spellingShingle |
Yanan Liu Haifeng Wang Huixin Dou Bin Tian Le Li Luyuan Jin Zhenting Zhang Lei Hu Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect Journal of Tissue Engineering |
author_facet |
Yanan Liu Haifeng Wang Huixin Dou Bin Tian Le Li Luyuan Jin Zhenting Zhang Lei Hu |
author_sort |
Yanan Liu |
title |
Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect |
title_short |
Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect |
title_full |
Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect |
title_fullStr |
Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect |
title_full_unstemmed |
Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect |
title_sort |
bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect |
publisher |
SAGE Publishing |
series |
Journal of Tissue Engineering |
issn |
2041-7314 |
publishDate |
2020-06-01 |
description |
Mesenchymal stem cells sheets have been verified as a promising non-scaffold strategy for bone regeneration. Alveolar bone marrow mesenchymal stem cells, derived from neural crest, have the character of easily obtained and strong multi-differential potential. However, the bone regenerative features of alveolar bone marrow mesenchymal stem cells sheets in the craniofacial region remain unclear. The purpose of the present study was to compare the osteogenic differentiation and bone defect repairment characteristics of bone marrow mesenchymal stem cells sheets derived from alveolar bone (alveolar bone marrow mesenchymal stem cells) and iliac bone (Lon-bone marrow mesenchymal stem cells) in vitro and in vivo . Histology character, osteogenic differentiation, and osteogenic gene expression of human alveolar bone marrow mesenchymal stem cells and Lon-bone marrow mesenchymal stem cells were compared in vitro . The cell sheets were implanted in rabbit calvarial defects to evaluate tissue regeneration characteristics. Integrated bioinformatics analysis was used to reveal the specific gene and pathways expression profile of alveolar bone marrow mesenchymal stem cells. Our results showed that alveolar bone marrow mesenchymal stem cells had higher osteogenic differentiation than Lon-bone marrow mesenchymal stem cells. Although no obvious differences were found in the histological structure, fibronectin and integrin β1 expression between them, alveolar-bone marrow mesenchymal stem cells sheet exhibited higher mineral deposition and expression levels of osteogenic marker genes. After being transplanted in the rabbit calvarial defects area, the results showed that greater bone volume and trabecular thickness regeneration were found in bone marrow mesenchymal stem cells sheet group compared to Lon-bone marrow mesenchymal stem cells group at both 4 weeks and 8 weeks. Finally, datasets of bone marrow mesenchymal stem cells versus Lon-bone marrow mesenchymal stem cells, and periodontal ligament mesenchymal stem cells (another neural crest derived mesenchymal stem cells) versus umbilical cord mesenchymal stem cells were analyzed. Total 71 differential genes were identified by overlap between the 2 datasets. Homeobox genes, such as LHX8, MKX, PAX9, MSX , and HOX , were identified as the most significantly changed and would be potential specific genes in neural crest mesenchymal stem cells. In conclusion, the Al-bone marrow mesenchymal stem cells sheet-based tissue regeneration appears to be a promising strategy for craniofacial defect repair in future clinical applications. |
url |
https://doi.org/10.1177/2041731420930379 |
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