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1.
Article in English | MEDLINE | ID: mdl-21147007

ABSTRACT

OBJECTIVE: Stem cells isolated from human dental follicles as a potential cell source for bone-tissue engineering were examined for correcting a critical bone defect. STUDY DESIGN: Impacted third molars were collected and single cell-derived cell populations were cultivated in growth medium. Single cell-derived cell lines were examined in terms of cell shape, gene expression patterns, differentiation capacity in vitro, and osteogenic potential in vivo. RESULTS: Three distinct cell populations were identified with different morphologies, patterns of gene expression, and differentiation capacity. All 3 cell populations promoted bone formation when transplanted into surgically created critical-size defects in immunodeficient rat calvaria, compared with control animals without cell transplantation, although one of these populations showed a weak capacity for osteogenetic differentiation in vitro. CONCLUSIONS: Human dental follicle can derive at least 3 unique cell populations in culture, all of which promote bone formation in vivo.


Subject(s)
Adult Stem Cells/transplantation , Bone Regeneration/physiology , Dental Sac/cytology , Osteogenesis/physiology , Stem Cell Transplantation , Adipogenesis/physiology , Adult Stem Cells/classification , Adult Stem Cells/cytology , Animals , Cell Differentiation , Cell Line , Chondrogenesis/physiology , Clone Cells/classification , Clone Cells/cytology , Clone Cells/transplantation , Humans , Rats , Rats, Inbred F344 , Skull/surgery , Transplantation, Heterologous
2.
Article in English | MEDLINE | ID: mdl-20123389

ABSTRACT

OBJECTIVES: Bacterial metabolites demineralize dental hard tissues, and soluble factors lead to tertiary dentinogenesis in the area of the dentin-pulp complex. However, it is unclear whether the oral bacteria are directly involved in the differentiation of dental pulp cells. In this study, we evaluated the effect of oral bacterial extracts on cellular differentiation in human dental pulp-derived cells (hDPC). STUDY DESIGN: The hDPC were obtained from third molar teeth, and the cells were subcultured. The sonicated extracts were obtained from Porphyromonas gingivalis (gram-negative) and Streptococcus mutans (gram-positive). The effect of bacterial extracts on cellular growth and differentiation in hDPC were tested. RESULTS: Alkaline phosphatase activity and bone sialoprotein (BSP) gene expression were increased in hDPC exposed to low concentrations of both sonicated extracts, whereas the activity was decreased upon exposure to high concentrations of sonicated extracts from P. gingivalis. CONCLUSION: This is the first evidence that oral bacteria have a positive effect on cellular differentiation in hPDC.


Subject(s)
Culture Media, Conditioned/pharmacology , Dental Pulp/drug effects , Dentinogenesis/drug effects , Osteogenesis/drug effects , Porphyromonas gingivalis , Streptococcus mutans , Analysis of Variance , Cell Differentiation/drug effects , Cell Proliferation/drug effects , Cells, Cultured , Dental Pulp/cytology , Dental Pulp/metabolism , Endotoxins , Extracellular Matrix Proteins/biosynthesis , Extracellular Matrix Proteins/genetics , Gene Expression , Humans , Integrin-Binding Sialoprotein , Phosphoproteins/biosynthesis , Phosphoproteins/genetics , Sialoglycoproteins/biosynthesis , Sialoglycoproteins/genetics , Sonication , Statistics, Nonparametric
3.
J Oral Sci ; 52(4): 541-52, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21206155

ABSTRACT

Adult stem cells are multipotent and can be induced experimentally to differentiate into various cell lineages. Such cells are therefore a key part of achieving the promise of tissue regeneration. The most studied stem cells are those of the hematopoietic and mesenchymal lineages. Recently, mesenchymal stem cells were demonstrated in dental tissues, including dental pulp, periodontal ligament, and dental follicle. The dental follicle is a loose connective tissue that surrounds the developing tooth. Dental follicle stem cells could therefore be a cell source for mesenchymal stem cells. Indeed, dental follicle is present in impacted teeth, which are commonly extracted and disposed of as medical waste in dental practice. Dental follicle stem cells can be isolated and grown under defined tissue culture conditions, and recent characterization of these stem cells has increased their potential for use in tissue engineering applications, including periodontal and bone regeneration. This review describes current knowledge and recent developments in dental follicle stem cells and their application.


Subject(s)
Adult Stem Cells , Dental Sac/cytology , Mesenchymal Stem Cells , Tissue Engineering , Animals , Cell Differentiation , Humans , Osteogenesis , Periodontal Ligament/cytology , Regeneration
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