Abstract
To explore the possible mechanism of osteogenesis for deciduous teeth stem cells (DTSCs) in vivo/ vitro, stem cells from goat deciduous teeth (SGDs) were firstly isolated, induced and transplanted into immunocompromised mice. The SGDs’s mineralization pattern and osteogenesis were compared with bone marrow messenchymal stem cells (BMMSCs) from goats. SGDs have similar osteogenic differentiation pattern in vitro and bone-like tissue formation mechanism in vivo to BMMSCs; moreover SGDs have stronger alkaline phosphatase (ALP) gene expression and osteopontin (OPN) gene expression levels than BMMSCs; also SGDs can form more bone-like tissues than BMMSCs when cell-scaffold compounds are transplanted into immunocompromised mice. This pre-clinical study in a large-animal model confirms that DTSCs may be an appropriate source of stem cells in repairing bone defects with tissue engineering.
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Gronthos S, Mankani M, Brahim J, et al. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo [J]. Proceedings of the National Academy of Sciences, 2000, 97(25): 13625–13630.
Miura M, Granthos S, Zhao M, et al. SHED: Stem cells from human exfoliated deciduous teeth [J]. Proceedings of the National Academy of Sciences, 2003, 100(10): 5807–5812.
Laino G, Graziano A, D’Aquino R, et al. An approachable human adult stem cell source for hardtissue engineering [J]. Journal of Cellular Physiology, 2006, 206(3): 693–701.
Seo B M, Sonoyama W, Yamaza T, et al. SHED repair critical-size calcarial defects in mice [J]. Oral Diseases, 2008, 14(5): 428–434.
Maniatopoulos C, Sodek J, Melcher A H. Bone formation in vitro by stromal cells obtained from bone marrow of young adult rats [J]. Cell Tissue Research, 1988, 254(2): 317–330.
Jiang X W, Zou S J, Ye B, et al. bFGF-modified BMMSCs enhance bone regeneration following distraction osteogenesis in rabbits [J]. Bone, 2010, 46(4): 1156–1161.
Zou D R, Gou L, Lu J Y, et al. Anatomic and histological analysis in a goat model used for maxillary sinus floor augmentation with simultaneous implant placement [J]. Clinical Oral Implant Research, 2010, 21(1): 65–70.
Wu L, Wu Y, Lin Y, et al. Osteogenic differentiation of adipose derived stem cells promoted by overexpression of osterix [J]. Molecular & Cellular Biochemistry, 2007, 301(1–2): 83–92.
Kenneth J, Thomas D. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method [J]. Methods, 2001, 25(4): 402–408.
Krebsbach P H, Kuznersov S A, Satomura K, et al. Bone formation in vivo: Comparison of osteogenesis by transplanted mouse and human marrow stromal fibroblasts [J]. Transplantation, 1997, 63(8): 1059–1069.
Pivoriunas A, Surovas A, Borutins K V, et al. Proteomic analysis of stromal cells derived from the dental pulp of human exfoliated deciduous teeth [J]. Stem Cells and Development, 2010, 19(7): 1081–1094.
Yamada Y, Nakamura S, Ito K, et al. A feasibility of useful cell-based therapy by bone regeneration with deciduous tooth stem cells dental pulp stem cells, bone marrow derived mesenchymal stem cells for clinical study using engineering technology [J]. Tissue Engineering: Part A, 2010. 16(6): 1891–1900.
Bruder S P, Jaiswal N, Hanesworth S E, et al. Growth kinetics, self-renewal, and the osteogenic potential of purified human mesenchymal stem cells during extensive subcultivation and following cryopreservation [J]. Journal of Cellular Biochemistry, 1997, 64(2): 278–294.
Locke M, Windsor J, Dunbar R R. Human adipose-derived stem cells: Isolation, characterization and application in surgery [J]. ANZ Journal of Surgery, 2009, 79(4): 235–244.
Yamada Y, Fujimoto A, Ito A, et al. Cluster analysis and gene expression profiles: A cDNA microarray system-based comparison between human dental pulp stem cells (hDPSCs) and human mesenchymal stem cells (hMSCs) for tissue engineering cell therapy [J]. Biomaterials, 2006, 27(20): 3766–3781.
Selim A A, Abdelmagid S M, Kanaan R A, et al. Anti-osteoactivin antibody inhibits osteoblast differentiation and function in vitro [J]. Critical Reviews in Eukaryotic Gene Expression, 2003, 13(2–4): 265–275.
Safadi F F, Xu J, Smock S L, et al. Cloning and characterization of osteoactivin a novel cDNA expressed in osteoblasts [J]. Journal of Cellular Biochemistry, 2001, 84(1): 12–26.
Seger D, Gechtman Z, Shaltiel S. Phosphorylation of vitronectin by casein kinase. II. Identification of the sites and their promotion of cell adhesion and spreading [J]. Journal of Biological Chemistry, 1998, 273(88): 24805–24813.
Suzuki Y, Kubota T, Koizami T, et al. Extracellular processing of bone and dentin proteins in matrix mineralization [J]. Connective Tissue Research, 1996, 35(1–4): 223–239.
Rifas L, Cheng S, Halstead L R, et al. Skeletal casein kinase activity defects in the HYR mouse [J]. Calcified Tissue International, 1997, 61(3): 256–259.
Selim A A, Castaneda J L, Owen T A, et al. The role of osteoactivin-derived peptides in osteoblast differentiation [J]. International Medical Journal for Experimental and Clinical Research, 2007, 13(12): 259–270.
Ohara N, Hayashi Y, Yamada S, et al. Early gene expression analyzed by cDNA microarray and RTPCR in osteoblasts cultured with water-soluble and low molecular chitooligosacharide [J]. Biomaterials, 2004, 25(10): 1749–1754.
Ogston N, Harrison A J, Cheung H F, et al. Dexamethasone and retinoic differentially regulate growth and differentiation in an immortalized human clonal bone marrow stromal cell line with osteoblastic [J]. Steroids, 2002, 67(11): 895–906.
Jørgensen N R, Henriksen Z, Sørensen O H, et al. Dexamethasone, BMP-2, and 1, 25-dihydroxyvitamin D enhance a more differentiated osteoblast phenotype: Validation of an in vitro model for human bone marrow-derived primary osteoblasts [J]. Steroids, 2004, 69(4): 219–226.
Zheng Y, Liu Y, Zhang C M, et al. Stem cells from deciduous tooth repair mandibular defect in swine [J]. Journal of Dental Research, 2009, 88(3): 249–254.
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Foundation item: the Science and Technology Commission fund of Shanghai Municipality (No. 09JC1411700), the Collaboration Projects of Development and Research from Basic Science of Stomatology of Shanghai (No. S30206-KF09), and the Fund of Shanghai Jiaotong University School of Medicine (No. 09XJ21030)
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Zhao, W., Lu, Jy., Hao, Ym. et al. Comparison of osteogenesis between two kinds of stem cells from goat combined calcium phosphate cement in tissue engineering. J. Shanghai Jiaotong Univ. (Sci.) 16, 628–635 (2011). https://doi.org/10.1007/s12204-011-1200-x
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DOI: https://doi.org/10.1007/s12204-011-1200-x
Key words
- stem cells from goat deciduous teeth (SGDs)
- mineralization
- osteogenesis
- bone marrow mesenchymal stem cells (BMMSCs)
- tissue engineering