Comparison of human optimized bacterial luciferase, firefly luciferase, and green fluorescent protein for continuous imaging of cell culture and animal models

被引:31
作者
Close, Dan M. [1 ]
Hahn, Ruth E. [1 ]
Patterson, Stacey S. [1 ]
Baek, Seung J. [2 ]
Ripp, Steven A. [1 ]
Sayler, Gary S. [1 ]
机构
[1] Univ Tennessee, Ctr Environm Biotechnol, Knoxville, TN 37996 USA
[2] Univ Tennessee, Coll Vet Med, Knoxville, TN 37996 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
bacterial luciferase; firefly luciferase; green fluorescent protein; optical imaging; bioluminescence;
D O I
10.1117/1.3564910
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bioluminescent and fluorescent reporter systems have enabled the rapid and continued growth of the optical imaging field over the last two decades. Of particular interest has been noninvasive signal detection from mammalian tissues under both cell culture and whole animal settings. Here we report on the advantages and limitations of imaging using a recently introduced bacterial luciferase (lux) reporter system engineered for increased bioluminescent expression in the mammalian cellular environment. Comparison with the bioluminescent firefly luciferase (Luc) system and green fluorescent protein system under cell culture conditions demonstrated a reduced average radiance, but maintained a more constant level of bioluminescent output without the need for substrate addition or exogenous excitation to elicit the production of signal. Comparison with the Luc system following subcutaneous and intraperitoneal injection into nude mice hosts demonstrated the ability to obtain similar detection patterns with in vitro experiments at cell population sizes above 2.5 x 10(4) cells but at the cost of increasing overall image integration time. (C) 2011 Society of Photo-Optical Instrumentation Engineers (SPIE). [DOI: 10.1117/1.3564910]
引用
收藏
页数:10
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