In Vivo Neuronal Cell Differentiation Imaging From Transplanted Stem Cells

被引:0
|
作者
Lee, Dong Soo [1 ]
机构
[1] Seoul Natl Univ, Grad Sch Convergence Sci & Technol, WCU Dept Mol Med & Biopharmaceut Sci, Coll Med,Dept Nucl Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Differentiation imaging; In vivo molecular imaging; Neuronal differentiation; Neuronal microRNA; Optical imaging; Stem cell therapy; GENE; EXPRESSION; MODELS; MOUSE;
D O I
暂无
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
In vivo cell tracking has been enabled by molecular imaging technology and, recently, monitoring cell fate changes has become possible in small animals. Stem cells and induced pluripotent stem cells (iPSCs) can differentiate in vivo after implantation, and lineage commitment of these cells can be successfully imaged using cell-specific promoter-driven reporter genes. For this purpose, imaging sensitivity has been significantly enhanced by engineering luciferase or adopting molecular amplification techniques. After transplantation of stem cells within a polymer scaffold, the fate changes of cells into neuronal lineages were monitored long enough to recognize possible adoption within endogenous microenvironment. Multiplexing and optimizing the imaging method to trace fate changes of transplanted stem cells can now be implemented broadly in vivo in small animals and possibly in humans.
引用
收藏
页码:278 / 283
页数:6
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