Advances in Cellular, Subcellular, and Nanoscale Imaging In Vitro and In Vivo

被引:47
|
作者
Wessels, Johannes T. [1 ]
Yamauchi, Kensuke [2 ,3 ]
Hoffman, Robert M. [2 ,3 ]
Wouters, Fred S. [4 ,5 ]
机构
[1] Univ Med Goettingen, Dept Nephrol & Rheumatol Mol & Opt Live Cell Imag, Ctr Internal Med, Gottingen, Germany
[2] AntiCancer Inc, San Diego, CA USA
[3] Univ Calif San Diego, Dept Surg, San Diego, CA 92103 USA
[4] Univ Med, Dept Neurophysiol, Gottingen, Germany
[5] DFG Res Ctr Mol Physiol Brair, CMPB, Gottingen, Germany
关键词
NIR; imaging; FRET; FLIM; STED; nanoscale; RED FLUORESCENT PROTEIN; RESONANCE ENERGY-TRANSFER; STIMULATED-EMISSION; STED MICROSCOPY; TURBID MEDIA; LIVING CELLS; TOMOGRAPHY; EXPRESSION; RESOLUTION; TUMORS;
D O I
10.1002/cyto.a.20931
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This review focuses on technical advances in fluorescence microscopy techniques including laser scanning techniques, fluorescence-resonance energy transfer (FRET) microscopy, fluorescence lifetime imaging (FLIM), stimulated emission depletion (STED)-based super-resolution microscopy, scanning confocal endomicroscopes, thin-sheet laser imaging microscopy (TSLIM), and tomographic techniques such as early photon tomography (EPT) as well as on clinical laser-based endoscopic and microscopic techniques We will also discuss the new developments in the field of fluorescent dyes and fluorescent genetic reporters that enable new possibilities in high-resolution and molecular imaging both in in vitro and in vivo. Small animal and tissue imaging benefit from the development of new fluorescent proteins, dyes, and sensing constructs that operate in the far red and near-infrared spectrum. (C) 2010 International Society for Advancement of Cytometry
引用
收藏
页码:667 / 676
页数:10
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