Zinc-modified titanium surface enhances osteoblast differentiation of dental pulp stem cells in vitro

被引:65
作者
Yusa, Kazuyuki [1 ]
Yamamoto, Osamu [2 ]
Takano, Hiroshi [3 ]
Fukuda, Masayuki [3 ]
Iino, Mitsuyoshi [1 ]
机构
[1] Yamagata Univ, Sch Med, Dept Dent Oral & Maxillofacial Plast & Reconstruc, Yamagata, Japan
[2] Yamagata Univ, Grad Sch Sci & Engn, Dept Biosyst Engn, Yonezawa, Yamagata, Japan
[3] Akita Univ, Sch Med, Div Dent & Oral Surg, Akita, Japan
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
BONE-FORMATION; TRICALCIUM PHOSPHATE; PROTEIN-SYNTHESIS; GROWTH; PROLIFERATION; FIBROBLASTS; BETA; OSTEOGENESIS; ANGIOGENESIS; EXPRESSION;
D O I
10.1038/srep29462
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Zinc is an essential trace element that plays an important role in differentiation of osteoblasts and bone modeling. This in vitro study aimed to evaluate the osteoblast differentiation of human dental pulp stem cells (DPSCs) on zinc-modified titanium (Zn-Ti) that releases zinc ions from its surface. Based on real-time PCR, alkaline phosphatase (ALP) activity and Western blot analysis data, we investigated osteoblast differentiation of DPSCs cultured on Zn-Ti and controls. DPSCs cultured on Zn-Ti exhibited significantly up-regulated gene expression levels of osteoblast-related genes of type I collagen (Col I), bone morphogenetic protein 2 (BMP2), ALP, runt-related transcription factor 2 (Runx2), osteopontin (OPN), and vascular endothelial growth factor A (VEGF A), as compared with controls. We also investigated extracellular matrix (ECM) mineralization by Alizarin Red S (ARS) staining and found that Zn-Ti significantly promoted ECM mineralization when compared with controls. These findings suggest that the combination of Zn-Ti and DPSCs provides a novel approach for bone regeneration therapy.
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页数:11
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