Epidermal growth factor enhances osteogenic differentiation of dental pulp stem cells in vitro

被引:47
|
作者
Del Angel-Mosqueda, Casiano [1 ,2 ,4 ]
Gutierrez-Puente, Yolanda [2 ,3 ]
Pricila Lopez-Lozano, Ada [1 ,2 ,4 ]
Emmanuel Romero-Zavaleta, Ricardo [1 ]
Mendiola-Jimenez, Andres [5 ]
Eduardo Medina-De la Garza, Carlos [1 ,5 ]
Marquez-M, Marcela [5 ,6 ]
Angelica De la Garza-Ramos, Myriam [1 ,4 ]
机构
[1] Univ Autonoma Nuevo Leon, Unidad Odontol Integral & Especialidades, Ctr Invest & Desarrollo Ciencias Salud, Monterrey, Nuevo Leon, Mexico
[2] Univ Autonoma Nuevo Leon, Inst Biotecnol, Fac Ciencias Biol, San Nicolas De Los Garza, Nuevo Leon, Mexico
[3] Univ Autonoma Nuevo Leon, Dept Quim, Fac Ciencias Biol, San Nicolas De Los Garza, Nuevo Leon, Mexico
[4] Univ Autonoma Nuevo Leon, Fac Odontol, Monterrey, Nuevo Leon, Mexico
[5] Univ Autonoma Nuevo Leon, Fac Med, Monterrey, Nuevo Leon, Mexico
[6] Karolinska Inst, CCK, Dept Oncol Pathol, Stockholm, Sweden
关键词
Dental pulp stem cells; Epidermal growth factor; Basic fibroblast growth factor; Osteogenic differentiation; Bone mineralization; Bone remodelling; ALKALINE-PHOSPHATASE EXPRESSION; BONE; MINERALIZATION; PROTEIN; PROLIFERATION; OSTEOBLASTS; EXPANSION; MATRIX;
D O I
10.1186/s13005-015-0086-5
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: Epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) play an important role in extracellular matrix mineralization, a complex process required for proper bone regeneration, one of the biggest challenges in dentistry. The purpose of this study was to evaluate the osteogenic potential of EGF and bFGF on dental pulp stem cells (DPSCs). Material and methods: Human DPSCs were isolated using CD105 magnetic microbeads and characterized by flow cytometry. To induce osteoblast differentiation, the cells were cultured in osteogenic medium supplemented with EGF or bFGF at a low concentration. Cell morphology and expression of CD146 and CD10 surface markers were analyzed using fluorescence microscopy. To measure mineralization, an alizarin red S assay was performed and typical markers of osteoblastic phenotype were evaluated by RT-PCR. Results: EGF treatment induced morphological changes and suppression of CD146 and CD10 markers. Additionally, the cells were capable of producing calcium deposits and increasing the mRNA expression to alkaline phosphatase (ALP) and osteocalcin (OCN) in relation to control groups (p < 0.001). However, bFGF treatment showed an inhibitory effect. Conclusion: These data suggests that DPSCs in combination with EGF could be an effective stem cell-based therapy for bone tissue engineering applications in periodontics and oral implantology.
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页数:9
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