Functional Selenium Nanoparticles Enhanced Stem Cell Osteoblastic Differentiation through BMP Signaling Pathways

被引:62
|
作者
Zheng, Chuping [1 ]
Wang, Jinsheng [2 ]
Liu, Yanan [1 ]
Yu, Qianqian [1 ]
Liu, Ying [1 ,3 ]
Deng, Ning [2 ]
Liu, Jie [1 ]
机构
[1] Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Guangdong Prov Key Lab Mol Immunol & Antibody Eng, Guangzhou 510632, Guangdong, Peoples R China
[3] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
PROMOTE OSTEOGENIC DIFFERENTIATION; MARROW STROMAL CELLS; UMBILICAL-CORD BLOOD; BONE-MARROW; GOLD NANOPARTICLES; MESENCHYMAL CELLS; HUMAN HEALTH; GROWTH; INHIBITION; PROLIFERATION;
D O I
10.1002/adfm.201401263
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stem cells have generated a great deal of excitement in tissue engineering and regenerative medicine, and it is important to understand the interaction mechanisms between nanomaterials and mesenchymal stem cells (MSCs) for biomedical applications. In this study, ruthenium (II) functional selenium nanoparticles (Ru@Se) are used for stem cell research. Specifically, Ru@Se are compared with citric acid selenium nanoparticles (Cit@Se) to identify their effects on MSCs differentiation and associated molecular mechanism. These data suggest that the effective adsorbing abilities of Ru@Se and Cit@Se allow them to act as preconcentration materials for osteogenic chemical inducers, which accelerates MSCs differentiation into osteoblasts. Further results suggest that selenium nanoparticles enhance the differentiation of MSCs toward osteogenic lineage over adipocytes by promoting osteogenic transcription and attenuating adipogenic transcription. Ru@Se and Cit@Se exert these effects by activating Smad-dependent BMP signaling pathway, which regulates the expression of relevant genes to induce osteogenic differentiation.
引用
收藏
页码:6872 / 6883
页数:12
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