Involvement of FAK/P38 Signaling Pathways in Mediating the Enhanced Osteogenesis Induced by Nano-Graphene Oxide Modification on Titanium Implant Surface

被引:53
|
作者
Li, Qingfan [1 ,2 ]
Wang, Zuolin [1 ,2 ]
机构
[1] Shanghai Engn Res Ctr Tooth Restorat & Regenerat, Shanghai, Peoples R China
[2] Tongji Univ, Hosp Stomatol, Sch Stomatol, Dept Oral Implant, Shanghai, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2020年 / 15卷
基金
中国国家自然科学基金;
关键词
graphene oxide; SLA; titanium implant; osteogenic differentiation; osseointegration; cell signaling pathways; FOCAL ADHESION KINASE; MARROW STROMAL CELLS; HYDROXYAPATITE BIOCERAMICS; OXIDATIVE STRESS; DENTAL IMPLANTS; STEM-CELL; DIFFERENTIATION; ANTIBACTERIAL; GROWTH; OSSEOINTEGRATION;
D O I
10.2147/IJN.S245608
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Titanium implants are widely used in dental and orthopedic medicine. Nevertheless, there is limited osteoinductive capability of titanium leading to a poor or delayed osseointegration, which might cause the failure of the implant therapy. Therefore, appropriate modification on the titanium surface for promoting osseointegration of existing implants is still pursued. Purpose: Graphene oxide (GO) is a promising candidate to perform implant surface biofunctionalization for modulating the interactions between implant surface and cells. So the objective of this study was to fabricate a bioactive GO-modified titanium implant surface with excellent osteoinductive potential and further investigate the underlying biological mechanisms. Materials and Methods: The large particle sandblasting and acid etching (SLA, commonly used in clinical practice) surface as a control group was first developed and then the nano-GO was deposited on the SLA surface via an ultrasonic atomization spraying technique to create the SLA/GO group. Their effects on rat bone marrow mesenchymal stem cells (BMSCs) responsive behaviors were assessed in vitro, and the underlying biological mechanisms were further systematically investigated. Moreover, the osteogenesis performance in vivo was also evaluated. Results: The results showed that GO coating was fabricated on the titanium substrates successfully, which endowed SLA surface with the improved hydrophilicity and protein adsorption capacity. Compared with the SLA surface, the GO-modified surface favored cell adhesion and spreading, and significantly improved cell proliferation and osteogenic differentiation of BMSCs in vitro. Furthermore, the FAK/P38 signaling pathways were proven to be involved in the enhanced osteogenic differentiation of BMSCs, accompanied by the upregulated expression of focal adhesion (vinculin) on the GO coated surface. The enhanced bone regeneration ability of GO-modified implants when inserted into rat femurs was also observed and confirmed that the GO coating induced accelerated osseointegration and osteogenesis in vivo. Conclusion: GO modification on titanium implant surface has potential applications for achieving rapid bone-implant integration through the mediation of FAK/P38 signaling pathways.
引用
收藏
页码:4659 / 4676
页数:18
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