Surface hydroxylation regulates cellular osteogeneses on TiO2 and Ta2O5 nanorod films

被引:12
|
作者
Wang, Liming [1 ]
Zhou, Beibei [1 ]
Liu, Zongguang [1 ]
Dong, Lingqing [1 ,2 ]
Cheng, Kui [1 ]
Weng, Wenjian [1 ]
机构
[1] Zhejiang Univ, State Key Lab Silicon Mat, Sch Mat Sci & Engn, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Stomatol Hosp, Hangzhou 310003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; Ta2O5; Osteogenic; Hydroxylation; Deprotonation rate; MESENCHYMAL STEM-CELLS; IMPLANT SURFACES; TITANIUM IMPLANT; BONE IMPLANTS; TANTALUM; DIFFERENTIATION; FIBRONECTIN; FABRICATION; NANOTUBES; MECHANISM;
D O I
10.1016/j.colsurfb.2018.04.012
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Titanium and tantalum have been widely used for orthopedic and dental implant applications. However, how their inherent surface features regulate cellular osteogeneses still remains elusive. In this study, we engineered two distinct TiO2 and Ta2O5 nanorod films as the two model oxidized surfaces to investigate their intrinsic osteogenic behaviors. The results indicated that the distinctive gradient on zeta potential against pH, corresponding to the deprotonation rate, but not the hydroxyl amount or hydroxylation polarity played a critical role on the cellular osteogenic performance. TiO2 nanorod film with a higher deprotonation rate significantly upregulated the expression of osteogeneses-related gene and protein, comparing to that of Ta2O5 nanorod film. These results might be attributed to that surface with higher deprotonation rateprovided more Bronsted acid-base surface sites to react with protein residues, leading to a mild change in conformation of the absorbed proteins, and subsequently facilitating to trigger the integrin focal adhesion cytoskeleton actin transduction pathway. This study, therefore, provides a new insight into the understanding the role of material surface hydroxylation on cellular osteogenic responses. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:213 / 219
页数:7
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