Assessment of proliferation, migration and differentiation potentials of bone marrow mesenchymal stem cells labeling with silica-coated and amine-modified superparamagnetic iron oxide nanoparticles
Assessment of proliferation, migration and differentiation potentials of bone marrow mesenchymal stem cells labeling with silica-coated and amine-modified superparamagnetic iron oxide nanoparticles
复制标题
二氧化硅包被和胺修饰的超顺磁性氧化铁纳米颗粒标记的骨髓间充质干细胞的增殖、迁移和分化潜能评估
DOI:
10.1007/s10616-020-00397-5
复制
发表时间:
2020-05
期刊:
影响因子:
2.2
通讯作者:
Mo B. W.
中科院分区:
文献类型:
--
作者:
Yao D;Liu N. N;Mo B. W.
Superparamagnetic iron oxide nanoparticles have been widely used for cell labeling in preclinical and clinical studies, to improve labeling efficiency, particle conjugation and surface modifications are developed, but some modified SPIONs exert side-effect on physiological activity of cells, which cannot be served as ideal cell tracker. In this study, amine-modified silica-coated SPIO (SPIO@SiO2-NH2, SPIO@S-N) nanoparticles were used to label bone marrow derived mesenchymal stem cells (BM-MSCs), then the stem cell potentials were evaluated. It was found BM-MSCs could be efficiently labeled by SPIO@S-N nanoparticles. After labeling, the BM-MSCs viability kept well and the migration ability increased, but the osteogenesis and adipogenesis potentials were not impaired. In steroid associated osteonecrosis (SAON) bone defect model, stem cell implantation was performed by injection of SPIO@S-N labeled BM-MSCs into marrow cavity locally, it was found the SPIO positive cells homed to the periphery of defect region in control group, but were recruited to the defect region in poly lactic-coglycolic acid/tricalcium phosphate (PLGA/TCP) scaffold implantation group. In conclusion, SPIO@S-N nanoparticles promoted migration while retained proliferation and differentiation ability of BM-MSCs, implying this kind of nanoparticles could be served not only an ideal tracking marker but also an accelerator for stem cell homing during tissue repair.
登录
查看更多内容
影响因子:
8
作者:
Kalber TL;Ordidge KL;Southern P;Loebinger MR;Kyrtatos PG;Pankhurst QA;Lythgoe MF;Janes SM
通讯作者:
Janes SM
DOI:
10.1007/978-1-61779-953-2_18
发表时间:
2012
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
Jasmin;Torres, Ana Luiza Machado;Jelicks, Linda;de Carvalho, Antonio Carlos Campos;Spray, David C;Mendez-Otero, Rosalia
通讯作者:
Mendez-Otero, Rosalia
影响因子:
14
作者:
Wang, Qiwei;Chen, Bo;Gu, Ning
通讯作者:
Gu, Ning
影响因子:
0.1
作者:
Cheng Wang;Yu Wang;H. Meng;Xue-ling Yuan;Xiao-long Xu;Ai-yuan Wang;Q. Guo;Jiang Peng;Shibi Lu
通讯作者:
Cheng Wang;Yu Wang;H. Meng;Xue-ling Yuan;Xiao-long Xu;Ai-yuan Wang;Q. Guo;Jiang Peng;Shibi Lu
影响因子:
3.8
作者:
Chen, Ying-Chun;Hsiao, Jong-Kai;Huang, Dong-Ming
通讯作者:
Huang, Dong-Ming