Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System

被引:36
作者
Yan, Jia [1 ]
Lu, Xiaoli [1 ]
Zhu, Xinchen [1 ]
Hu, Xiaokun [1 ]
Wang, Lili [1 ]
Qian, Jun [1 ]
Zhang, Feimin [1 ]
Liu, Mei [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp Stomatol, Dept Prosthodont, Jiangsu Key Lab Oral Dis, Nanjing 210029, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2020年 / 15卷
关键词
nanocarrier; microRNAs; osteoinduction; tissue engineering; DELIVERY-SYSTEM; SIRNA DELIVERY; GENE DELIVERY; REGENERATION; SCAFFOLDS; BIOMATERIALS; REPAIR; ROLES; RNA;
D O I
10.2147/IJN.S228797
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Introduction: RNA-based therapy for bone repair and regeneration is a highly safe and effective approach, which has been extensively investigated in recent years. However, the molecular stability of RNA agents still remains insufficient for clinical application. High porosity, tunable size, and ideal biodegradability and biosafety are a few of the characters of mesoporous silicon nanoparticles (MSNs) that render them a promising biomaterial carrier for RNA treatment. Materials and Methods: In this study, a novel miR-26a delivery system was constructed based on MSNs. Next, we assessed the miRNA protection of the delivery vehicles. Then, rat bone marrow mesenchymal stem cells (rBMSCs) were incubated with the vectors, and the transfection efficiency, cellular uptake, and effects on cell viability and osteogenic differentiation were evaluated. Results: The results demonstrated that the vectors protected miR-26a from degradation in vitro and delivered it into the cytoplasm. A relatively low concentration of the delivery systems significantly increased osteogenic differentiation of rBMSCs. Conclusion: The vectors constructed in our study provide new methods and strategies for the delivery of microRNAs in bone tissue engineering.
引用
收藏
页码:497 / 511
页数:15
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