Human adipose-derived stem cells and simvastatin-functionalized biomimetic calcium phosphate to construct a novel tissue-engineered bone

被引:14
|
作者
Zhang, Xiao [1 ,2 ]
Jiang, Weiran [1 ,2 ]
Liu, Yunsong [1 ,2 ]
Zhang, Ping [1 ,2 ]
Wang, Linchuan [1 ,2 ]
Li, Wenyue [1 ,2 ]
Wu, Gang [3 ,4 ]
Ge, Yanjun [1 ,2 ]
Zhou, Yongsheng [1 ,2 ]
机构
[1] Peking Univ, Dept Prosthodont, Sch & Hosp Stomatol, Beijing 100081, Peoples R China
[2] Peking Univ, Natl Engn Lab Digital & Mat Technol Stomatol, Sch & Hosp Stomatol, Beijing Key Lab Digital Stomatol, Beijing 100081, Peoples R China
[3] Univ Amsterdam, Dept Oral Implantol & Prosthet Dent, Acad Ctr Dent Amsterdam ACTA, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Amsterdam, Netherlands
基金
中国国家自然科学基金;
关键词
Human adipose-derived stem cells; Simvastatin; Biomimetic; Calcium phosphate; Tissue-engineered bone; LOADED PLGA MICROSPHERES; OSTEOGENESIS; REGENERATION; DEFECTS; RELEASE; COMBINATION; SCAFFOLDS;
D O I
10.1016/j.bbrc.2017.11.150
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To repair bone defects, we evaluate the in-vitro and in-vivo osteogenic activities of a novel tissue-engineered bone (TEB) by elaborately combining biomimetic calcium phosphate (BioCaP) granules with internally-incorporated simvastatin (SIM) and human adipose-derived stem cells (hASCs). First, we constructed BioCaP with SIM internally incorporated (SIM-BioCaP). Then we characterized the morphology and chemical composition of SIM-BioCaP. The release kinetics of SIM was monitored in vitro spectroscopically. Thereafter, we explored the in-vitro cellular responses of hASCs to SIM-BioCaP by performing scanning electron microscopy observation, proliferation assay, alkaline phosphatase (ALP) activity assay, alizarin red staining and real-time PCR Finally, we investigated the in-vivo osteogenic activities of the novel TEB in a subcutaneous bone induction model in nude mice. We found that SIM was successfully incorporated internally in BioCaP and showed a slow release manner without significantly affecting the attachment and proliferation of hASCs. The released SIM from BioCaP could significantly enhance the proliferation, ALP activities, mineralized nodules formation and osteogenic genes of hASCs. The in-vivo tests showed this TEB could induce new bone formation while the other groups could not. Taken together, the present data show that this novel TEB represented a very promising construct to treat critical-volume bone defects. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1264 / 1270
页数:7
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