Mineralized and osteoid tissue from dental pulp stem cells on micro-arc oxidation titanium in vitro

Yi Huang , Ting Chang , Cheng Yang , Mengjuan Wu

Current Medical Science ›› 2012, Vol. 32 ›› Issue (4) : 620 -625.

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Current Medical Science ›› 2012, Vol. 32 ›› Issue (4) : 620 -625. DOI: 10.1007/s11596-012-1007-5
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Mineralized and osteoid tissue from dental pulp stem cells on micro-arc oxidation titanium in vitro

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Abstract

The presence of insufficient bone volume affects the implant healing and success. The aim of this study was to evaluate osteogenic capacity of dental pulp stem cells (DPSCs) on micro-arc oxidation (MAO) titanium surface. DPSCs were challenged at MAO and smooth titanium surface separately for different durations, and the bone marrow mesenchymal stem cells (BMSCs) served as the positive controls. The osteogenic capacity of DPSCs on MAO titanium surface was assessed by using scanning electron microscopy, energy dispersive spectroscopy, biochemical tests and real-time quantitative PCR. Data showed that DPSCs differentiated into osteoblasts and expressed bone morphogenetic genes on MAO titanium surface. The results of this study revealed that DPSCs had good potential to generate mineralized tissue on MAO titanium plates. The differential potential of DPSCs may be regulated by MAO titanium surface. The osteogenesis potential of DPSCs on the MAO titanium was similar with BMSCs.

Keywords

dental pulp stem cells / micro-arc oxidation / osteogenic differentiation / mineralized tissue / dental implant

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Yi Huang, Ting Chang, Cheng Yang, Mengjuan Wu. Mineralized and osteoid tissue from dental pulp stem cells on micro-arc oxidation titanium in vitro. Current Medical Science, 2012, 32(4): 620-625 DOI:10.1007/s11596-012-1007-5

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References

[1]

DaviesJ.E.. Understanding peri-implant endosseous healing. J Dent Educ, 2003, 67(8): 932-949

[2]

LangerB., LangerL., SullivanR.M.. Vertical ridge augmentation procedure using guided bone regeneration, demineralized freeze-dried bone allograft, and miniscrews: 4- to 13-year observations on loaded implants. Int J Periodontics Restorative Dent, 2010, 30(3): 227-235

[3]

ChiapascoM., CasentiniP., ZaniboniM.. Bone augmentation procedures in implant dentistry. Int J Oral Maxillofac Implants, 2009, 24: 237-2359

[4]

RocchiettaI., FontanaF., SimionM.. Clinical outcomes of vertical bone augmentation to enable dental implant placement: a systematic review. J Clin Periodontol, 2008, 35(8): 203-215

[5]

PierdomenicoL., BonsiL., CalvittiM., et al.. Multipotent mesenchymal stem cells with immunosuppressive activity can be easily isolated from dental pulp. Transplantation, 2005, 80(6): 836-842

[6]

EdwardsR.G.. Stem cells today: B1. Bone marrow stem cells. Reprod Biomed Online, 2004, 9(5): 541-583

[7]

GiannoniP., MuragliaA., GiordanoC., et al.. Osteogenic differentiation of human mesenchymal stromal cells on surface-modified titanium alloys for orthopedic and dental implants. Int J Artif Organs, 2009, 32(11): 811-820

[8]

YamadaY., FujimotoA., ItoA., 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. Biomaterials, 2006, 27(20): 3766-3781

[9]

GrazianoA., d’AquinoR., LainoG., et al.. Dental pulp stem cells: a promising tool for bone regeneration. Stem Cell Rev, 2008, 4(1): 21-26

[10]

KoyamaN., OkuboY., NakaoK., et al.. Evaluation of pluripotency in human dental pulp cells. J Oral Maxillofac Surg, 2009, 67(3): 501-506

[11]

SonoyamaW., LiuY., YamazaT., et al.. Characterization of the apical papilla and its residing stem cells from human immature permanent teeth: a pilot study. J Endod, 2008, 34(2): 166-171

[12]

ManganoC., De RosaA., DesiderioV., et al.. The osteoblastic differentiation of dental pulp stem cells and bone formation on different titanium surface textures. Biomaterials, 2010, 31(13): 3543-3551

[13]

TrubianiO., OrsiniG., CaputiS., et al.. Adult mesenchymal stem cells in dental research: a new approach for tissue engineering. Int J Immunopathol Pharmacol, 2006, 19(3): 451-460

[14]

YamadaY., NakamuraS., ItoK., et al.. A feasibility of useful cell-based therapy by bone regeneration with deciduous tooth stem cells, dental pulp stem cells, or bone-marrow-derived mesenchymal stem cells for clinical study using tissue engineering technology. Tissue Eng Part A, 2010, 16(6): 1891-1900

[15]

YangC., MengL., TianY., et al.. Cytotoxicity study of a novel implant material modified by microarc oxidation. J Huazhong Univ Sci Technolog Med Sci, 2006, 26(6): 720-722

[16]

KarageorgiouV., KaplanD.. Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials, 2005, 26(27): 5474-5491

[17]

KomoriT.. Regulation of bone development and extracellular matrix protein genes by RUNX2. Cell Tissue Res, 2010, 339(1): 189-195

[18]

ZhouX., ZhangZ., FengJ.Q., et al.. Multiple functions of Osterix are required for bone growth and homeostasis in postnatal mice. Proc Natl Acad Sci USA, 2010, 107(29): 12 919-12 924

[19]

RoodmanG.D.. Osteoblast function in myeloma. Bone, 2011, 48(1): 135-140

[20]

TowlerD.A., ShaoJ.S., ChengS.L., et al.. Osteogenic regulation of vascular calcification. Ann N Y Acad Sci, 2006, 1068: 327-333

[21]

UnterbrinkA., O’sullivanM., ChenS., et al.. TGF beta-1 downregulates DMP-1 and DSPP in odontoblasts. Connect Tissue Res, 2002, 43(2–3): 354-358

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