SCORE Imaging: Specimen in a Corrected Optical Rotational Enclosure

被引:49
作者
Petzold, Andrew M. [1 ,2 ]
Bedell, Victoria M. [1 ]
Boczek, Nicole J. [1 ,3 ]
Essner, Jeffrey J. [4 ]
Balciunas, Darius [2 ,5 ]
Clark, Karl J. [1 ]
Ekker, Stephen C. [1 ,2 ]
机构
[1] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Univ Minnesota, Minneapolis, MN USA
[3] St Olaf Coll, Dept Biol, Northfield, MN 55057 USA
[4] Iowa State Univ, Dept Genet Dev & Cell Biol, Ames, IA USA
[5] Temple Univ, Dept Biol, Philadelphia, PA 19122 USA
关键词
REFRACTIVE-INDEX; ZEBRAFISH; TRANSPOSON; GENETICS;
D O I
10.1089/zeb.2010.0660
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Visual data collection is paramount for the majority of scientific research. The added transparency of the zebrafish (Danio rerio) allows for a greater detail of complex biological research that accompanies seemingly simple observational tools. We developed a visual data analysis and collection approach that takes advantage of the cylindrical nature of the zebrafish allowing for an efficient and effective method for image capture that we call Specimen in a Corrected Optical Rotational Enclosure imaging. To achieve a nondistorted image, zebrafish were placed in a fluorinated ethylene propylene tube with a surrounding optically corrected imaging solution (water). By similarly matching the refractive index of the housing (fluorinated ethylene propylene tubing) to that of the inner liquid and outer liquid (water), distortion was markedly reduced, producing a crisp imagable specimen that is able to be fully rotated 360 degrees. A similar procedure was established for fixed zebrafish embryos using convenient, readily available borosilicate capillaries surrounded by 75% glycerol. The method described here could be applied to chemical genetic screening and other related high-throughput methods within the fish community and among other scientific fields.
引用
收藏
页码:149 / 154
页数:6
相关论文
共 19 条
[1]  
[Anonymous], 1999, POLYM HDB
[2]   FishNet: an online database of zebrafish anatomy [J].
Bryson-Richardson, Robert J. ;
Berger, Silke ;
Schilling, Thomas F. ;
Hall, Thomas E. ;
Cole, Nicholas J. ;
Gibson, Abigail J. ;
Sharpe, James ;
Currie, Peter D. .
BMC BIOLOGY, 2007, 5 (1)
[3]   Zebrafish myelination: a transparent model for remyelination? [J].
Buckley, Clare E. ;
Goldsmith, Paul ;
Franklin, Robin J. M. .
DISEASE MODELS & MECHANISMS, 2008, 1 (4-5) :221-228
[4]   REFRACTIVE-INDEX MATCHING METHODS FOR LIQUID FLOW INVESTIGATIONS [J].
BUDWIG, R .
EXPERIMENTS IN FLUIDS, 1994, 17 (05) :350-355
[5]   Efficient gene delivery and gene expression in zebrafish using the Sleeping Beauty transposon [J].
Davidson, AE ;
Balciunas, D ;
Mohn, D ;
Shaffer, J ;
Hermanson, S ;
Sivasubbu, S ;
Cliff, MP ;
Hackett, PB ;
Ekker, SC .
DEVELOPMENTAL BIOLOGY, 2003, 263 (02) :191-202
[6]   Micro fluid segment technique for screening and development studies on Danio rerio embryos [J].
Funfak, Anette ;
Broesing, Andreas ;
Brand, Michael ;
Koehler, Johann Michael .
LAB ON A CHIP, 2007, 7 (09) :1132-1138
[7]  
Kerbow D., 1999, POLYM HDB
[8]   STAGES OF EMBRYONIC-DEVELOPMENT OF THE ZEBRAFISH [J].
KIMMEL, CB ;
BALLARD, WW ;
KIMMEL, SR ;
ULLMANN, B ;
SCHILLING, TF .
DEVELOPMENTAL DYNAMICS, 1995, 203 (03) :253-310
[9]   In vivo imaging of embryonic vascular development using transgenic zebrafish [J].
Lawson, ND ;
Weinstein, BM .
DEVELOPMENTAL BIOLOGY, 2002, 248 (02) :307-318
[10]   MICROSCOPY AND MANIPULATION OF CELLS IN ELASTIC CAPILLARIES [J].
MOROZ, PE .
TRANSACTIONS OF THE AMERICAN MICROSCOPICAL SOCIETY, 1994, 113 (03) :412-414