The promotion of osteointegration under diabetic conditions using chitosan/hydroxyapatite composite coating on porous titanium surfaces

被引:98
作者
Ma, Xiang-Yu [1 ]
Feng, Ya-Fei [1 ]
Ma, Zhen-Sheng [1 ]
Li, Xiang [2 ]
Wang, Jian [1 ]
Wang, Lin [1 ]
Lei, Wei [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Orthoped, Xian 710032, Shaanxi, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Mech Engn, State Key Lab Mech Syst & Vibrat, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous titanium; Diabetes; Wnt/beta-catenin; Chitosan; Hydroxyapatite; WNT/BETA-CATENIN PATHWAY; MESENCHYMAL STEM-CELLS; WNT SIGNALING PATHWAY; GLYCEMIC CONTROL; BONE-FORMATION; CHITOSAN; MELLITUS; DIFFERENTIATION; OSSEOINTEGRATION; ACTIVATION;
D O I
10.1016/j.biomaterials.2014.05.028
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Composited Chitosan/Hydroxyapatite (CS/HA) material coated on titanium surface (cTi) is a promising approach to produce biomaterials with better osseointegration capacity, but its bio-performance under diabetic conditions and the mechanisms involved remain elusive. We propose that the alterations in the Wnt/beta-catenin pathway may play a role in mediating the improvement effect of cTi on diabetes-induced impaired implant osteointegration. To confirm the hypothesis, primary rat osteoblasts incubated on Ti and cTi were subjected to normal serum (NS), diabetic serum (DS), DS + Wnt3a (a specific Wnt agonist) and DS + Dkk1 (a specific Wnt antagonist) treatment. In vivo study was performed on diabetic sheep implanted with Ti or cTi into the bone defect on crista iliaca. Results showed that diabetes depressed osteoblast function evidenced by impaired cell adhesion and morphology, decreased cell proliferation and ALP activity, and higher apoptotic rate on Ti. Importantly, both cTi and Wnt3a treatment ameliorated osteoblastic dysfunction and apoptosis under diabetic condition. Implantation with cTi significantly improved osteointegration evidenced by Micro-CT and histological examinations compared with Ti. Moreover, the aforementioned promotive effects afforded by cTi were abolished by blocking Wnt pathway with Dkk1. Our study explicitly demonstrates that CS/HA composite material improves diabetes-induced impaired osteointegration of Ti via the reactivation of Wnt/beta-catenin pathway and provides a target point for biomaterial modification to attain better clinical performance in diabetic patients. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7259 / 7270
页数:12
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