Long-working-distance fluorescence microscope with high-numerical-aperture objectives for variable-magnification imaging in live mice from macro- to subcellular

被引:16
作者
Kimura, Hiroaki [1 ,2 ,3 ]
Momiyama, Masashi [1 ,2 ,4 ]
Tomita, Katsuro [3 ]
Tsuchiya, Hiroyuki [3 ]
Hoffman, Robert M. [1 ,2 ]
机构
[1] AntiCanc Inc, San Diego, CA 92111 USA
[2] Univ Calif San Diego, Dept Surg, San Diego, CA 92103 USA
[3] Kanazawa Univ, Grad Sch Med Sci, Dept Orthopaed Surg, Kanazawa, Ishikawa, Japan
[4] Yokohama City Univ, Dept Surg Gastroenterol, Grad Sch Med, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
关键词
green fluorescent protein; red fluorescent protein; mice; subcellular imaging; fluorescence microscopy; in vivo cell biology; REAL-TIME; IN-VIVO; CELLULAR-DYNAMICS; CANCER; METASTASIS; CELLS; PROGRESSION; MOUSE;
D O I
10.1117/1.3526356
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We demonstrate the development of a long-working-distance fluorescence microscope with high-numerical-aperture objectives for variable-magnification imaging in live mice from macro- to subcellular. To observe cytoplasmic and nuclear dynamics of cancer cells in the living mouse, 143B human osteosarcoma cells are labeled with green fluorescent protein in the nucleus and red fluorescent protein in the cytoplasm. These dual-color cells are injected by a vascular route in an abdominal skin flap in nude mice. The mice are then imaged with the Olympus MVX10 macroview fluorescence microscope. With the MVX10, the nuclear and cytoplasmic behavior of cancer cells trafficking in blood vessels of live mice is observed. We also image lung metastases in live mice from the macro- to the subcellular level by opening the chest wall and imaging the exposed lung in live mice. Injected splenocytes, expressing cyan fluorescent protein, could also be imaged on the lung of live mice. We demonstrate that the MVX10 microscope offers the possibility of full-range in vivo fluorescence imaging from macro- to subcellular and should enable widespread use of powerful imaging technologies enabled by genetic reporters and other fluorophores. (C) 2010 Society of Photo-Optical Instrumentation Engineers. [DOI: 10.1117/1.3526356]
引用
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页数:6
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