In vivo imaging in experimental preclinical tumor research - A review

被引:86
作者
Wessels, J. T.
Busse, A. C.
Mahrt, J.
Dullin, C.
Grabbe, E.
Mueller, G. A.
机构
[1] Univ Hosp Gottingen, Dept Nephrol Rheumatol, Ctr Internal Med, D-37099 Gottingen, Germany
[2] Univ Hosp Gottingen, Dept Diagnost Radiol, Ctr Radiol, D-37099 Gottingen, Germany
关键词
molecular imaging; optical imaging; tumor imaging; fpVCT; near infrared range imaging; renal cell carcinoma; in vivo cytometry; fluorescence in vivo imaging;
D O I
10.1002/cyto.a.20419
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The multiparametric molecular cell and tissue analysis in vitro and in vivo is characterized by rapid progress in the field of image generation technologies, sensor biotechnology, and computational modeling. Fascinating new potentials in unraveling the detailed functions of single cells, organs, and whole organisms are presently emerging and permit the close monitoring i.e. tumor development or basic cell development processes with an unprecedented multiplicity of promising investigative possibilities. To answer basic questions of in vivo tumor development and progression fluorescence based imaging techniques provide new insights into molecular pathways and targets. Genetic reporter systems (eGFP, DsRED) are available and high sensitive detection systems are on hand. These techniques could be used for in vitro assays and quantified e.g. by microscopy and CCD based readouts. The introduction of novel fluorescent dyes emitting in the near infrared range (NIR) combined with the development of sensitive detector Systems and monochromatic powerful NIR-lasers for the first time permits the quantification and imaging of fluorescence and/or bioluminescence in deeper tissues. Laser based techniques particularly in the NIR-range (like two-photon microscopy) offer superb signal to noise ratios, and thus the potential to detect molecular targets in vivo. In combination with flat panel volumetric computed tomography (fpVCT), questions dealing e.g. with tumor size, tumor growth, and angiogenesis/vascularization could be answered noninvasively using the same animal. The resolution of down to 150 mu m/each direction can be achieved using fpVCT. It is demonstrated by many groups that submillimeter resolutions can be achieved in small animal imaging at high sensitivity and molecular specificity. Since the resolution in preclinical small animal imaging is down to similar to 10 pm by the use of microCT and to subcellular resolutions using (similar to 1 mu m) microscope based systems, the advances of different techniques can now be combined to "multimodal" preclinical imaging and the possibilities for in vivo intravital cytometry now become within one's reach. (C) 2007 International Society for Analytical Cytology
引用
收藏
页码:542 / 549
页数:8
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