Multispectral opto-acoustic tomography of deep-seated fluorescent proteins in vivo

被引:554
作者
Razansky, Daniel [1 ]
Distel, Martin [2 ]
Vinegoni, Claudio [3 ,4 ]
Ma, Rui [1 ]
Perrimon, Norbert [5 ,6 ]
Koester, Reinhard W. [2 ]
Ntziachristos, Vasilis [1 ]
机构
[1] Tech Univ Munich, Inst Biol & Med Imaging, D-85764 Neuherberg, Germany
[2] Helmholtz Ctr Munich, Inst Dev Genet, D-85764 Neuherberg, Germany
[3] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Richard B Simches Res Ctr, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[6] Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
HIGH-RESOLUTION; MICROSCOPY; BRAIN;
D O I
10.1038/NPHOTON.2009.98
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Fluorescent proteins have become essential reporter molecules for studying life at the cellular and sub-cellular level, re-defining the ways in which we investigate biology. However, because of intense light scattering, most organisms and tissues remain inaccessible to current fluorescence microscopy techniques at depths beyond several hundred micrometres. We describe a multispectral opto-acoustic tomography technique capable of high-resolution visualization of fluorescent proteins deep within highly light-scattering living organisms. The method uses multiwavelength illumination over multiple projections combined with selective-plane opto-acoustic detection for artifact-free data collection. Accurate image reconstruction is enabled by making use of wavelength-dependent light propagation models in tissue. By performing whole-body imaging of two biologically important and optically diffuse model organisms, Drosophila melanogaster pupae and adult zebrafish, we demonstrate the facility to resolve tissue-specific expression of eGFP and mCherrry fluorescent proteins for precise morphological and functional observations in vivo.
引用
收藏
页码:412 / 417
页数:6
相关论文
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[31]  
2007, NATURE METHODS, V4, P463