神经突
氧化铁纳米粒子
材料科学
纳米颗粒
细胞生物学
神经生长因子
氧化铁
生物物理学
细胞粘附
MAPK/ERK通路
粘附
纳米技术
信号转导
化学
体外
生物
生物化学
受体
冶金
复合材料
作者
Jeong Ah Kim,Jeong Yong Lee,Byung Hyo Kim,Won Jong Rhee,Sungjun Yoon,Taeghwan Hyeon,Tai Hyun Park
出处
期刊:Biomaterials
[Elsevier]
日期:2011-02-02
卷期号:32 (11): 2871-2877
被引量:123
标识
DOI:10.1016/j.biomaterials.2011.01.019
摘要
Despite the many potential therapeutic applications of iron oxide nanoparticle such as its use as an imaging and targeting tool, its biological effects have not yet been extensively characterized. Herein, we report that iron oxide nanoparticles taken up by PC12 cells can enhance neurite outgrowth. PC12 cells exposed to both iron oxide nanoparticles and nerve growth factor (NGF) synergistically increased the efficiency of neurite outgrowth in a dose-dependent manner. This may have resulted from the activation of cell adhesion molecules that are associated with cell-matrix interactions through iron. Immunoblotting assays also revealed that both neural specific marker protein and cell adhesion protein expression were upregulated by iron oxide nanoparticles compared with non-treated cells via activation of the mitogen-activated protein kinase (MAPK) signaling pathway. Our findings point to the possibility that iron oxide nanoparticles can affect cell-substrate interactions and regulate cell behaviors, which provides clinical insights into potential neurologic and therapeutic applications of iron oxide nanoparticles.
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