Bioluminescence imaging in live cells and animals

被引:46
|
作者
Tung, Jack K. [1 ,2 ]
Berglund, Ken [2 ]
Gutekunst, Claire-Anne [2 ]
Hochgeschwender, Ute [3 ,4 ]
Gross, Robert E. [1 ,2 ]
机构
[1] Georgia Inst Technol, Coulter Dept Biomed Engn, 313 Ferst Dr,Room 2127, Atlanta, GA 30332 USA
[2] Emory Univ, Dept Neurosurg, 101 Woodruff Circle,WMRB Rm 6337, Atlanta, GA 30322 USA
[3] Cent Michigan Univ, Coll Med, 1280 S East Campus St, Mt Pleasant, MI 48859 USA
[4] Cent Michigan Univ, Dept Neurosci, Neurosci Program, 1280 S East Campus St, Mt Pleasant, MI 48859 USA
基金
美国国家科学基金会;
关键词
bioluminescence; luciferase; imaging; live cell; in vivo; GREEN FLUORESCENT PROTEIN; RESONANCE ENERGY-TRANSFER; NEURAL STEM-CELLS; IN-VIVO; LUMINESCENT PROTEINS; LIVING SUBJECTS; SINGLE-CELL; REPORTER; BRAIN; LUCIFERASES;
D O I
10.1117/1.NPh.3.2.025001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The use of bioluminescent reporters in neuroscience research continues to grow at a rapid pace as their applications and unique advantages over conventional fluorescent reporters become more appreciated. Here, we describe practical methods and principles for detecting and imaging bioluminescence from live cells and animals. We systematically tested various components of our conventional fluorescence microscope to optimize it for long-term bioluminescence imaging. High-resolution bioluminescence images from live neurons were obtained with our microscope setup, which could be continuously captured for several hours with no signs of phototoxicity. Bioluminescence from the mouse brain was also imaged noninvasively through the intact skull with a conventional luminescence imager. These methods demonstrate how bioluminescence can be routinely detected and measured from live cells and animals in a cost-effective way with common reagents and equipment. (C) The Authors.
引用
收藏
页数:6
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