Effects of two fast-setting pulp-capping materials on cell viability and osteogenic differentiation in human dental pulp stem cells: An in vitro study

被引:11
作者
Sun, Yan [1 ,2 ]
Liu, Jun [3 ]
Luo, Tao [1 ]
Shen, Ya [4 ]
Zou, Ling [1 ]
机构
[1] Sichuan Univ, State Key Lab Oral Dis, Natl Clin Res Ctr Oral Dis, Dept Conservat Dent & Endodont,West China Sch & H, Chengdu 610041, Sichuan, Peoples R China
[2] Wenzhou Med Univ, Dept Conservat Dent & Endodont, Sch & Hosp Stomatol, Wenzhou 325027, Peoples R China
[3] Sichuan Univ, State Key Lab Oral Dis, Natl Clin Res Ctr Oral Dis, Dept Orthodont,West China Sch & Hosp Stomatol, Chengdu 610041, Sichuan, Peoples R China
[4] Univ British Columbia, Div Endodont, Dept Oral Biol & Med Sci, Fac Dent, Vancouver, BC, Canada
基金
中国国家自然科学基金;
关键词
Biodentine (BD); iRoot fast set root repair material (FS); Pulp capping; Cell viability; Osteogenic differentiation; Human dental pulp stem cells (hDPSCs); MINERAL TRIOXIDE AGGREGATE; CALCIUM-SILICATE CEMENTS; CLINICAL-APPLICATIONS; BIOACTIVE CEMENTS; BIODENTINE; ADHESION; BIOCOMPATIBILITY; PROLIFERATION; TOPOGRAPHY; PHOSPHATE;
D O I
10.1016/j.archoralbio.2019.02.014
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: The purpose of this study was to compare the effects of two fast-setting pulp-capping materials, Biodentine (BD) and iRoot Fast Set (FS) root repair material, on the attachment, viability, migration, and differentiation of human dental pulp stem cells (hDPSCs). Methods: A comparative study was conducted between BD and FS material disks. Scanning electron microscope (SEM) images were used to observe the attachment of hDPSCs on the disks. A live/dead assay was used to assess the cell viability. Transwell assay was performed to study cell migration. Cell differentiation was determined by quantitative real-time polymerase chain reaction (qRT-PCR) for the analysis of osteogenic differentiation gene expression: alkaline phosphatase (ALP), collagen type I (COL1) and osteocalcin (OCN). Results: SEM images indicated that hDPSCs showed a well-spreading morphology on both BD and FS disks. FS significantly increased the proliferation and migration of hDPSCs on day 7 (P < 0.05). Neither BD nor FS promoted the expression of osteogenic genes during the observation period. Conclusions: BD and FS both were beneficial to hDPSC attachment, and they had similar effects on cell osteogenic differentiation, whereas FS performed better than BD on hDPSCs proliferation and migration.
引用
收藏
页码:100 / 105
页数:6
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