Single Plane Illumination Module and Micro-capillary Approach for a Wide-field Microscope

被引:14
作者
Bruns, Thomas [1 ]
Schickinger, Sarah [1 ]
Schneckenburger, Herbert [1 ]
机构
[1] Aalen Univ, Inst Appl Res, Aalen, Germany
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2014年 / 90期
关键词
Physics; Issue; 90; Fluorescence; light sheet; single plane illumination microscopy (SPIM); 3D cell cultures; rectangular capillary; microfluidics; multi-cellular tumor spheroids (MCTS); wide-field microscopy; FLUORESCENCE MICROSCOPY; LIGHT; MODEL;
D O I
10.3791/51993
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A module for light sheet or single plane illumination microscopy (SPIM) is described which is easily adapted to an inverted wide-field microscope and optimized for 3-dimensional cell cultures, e. g., multi-cellular tumor spheroids (MCTS). The SPIM excitation module shapes and deflects the light such that the sample is illuminated by a light sheet perpendicular to the detection path of the microscope. The system is characterized by use of a rectangular capillary for holding (and in an advanced version also by a micro-capillary approach for rotating) the samples, by synchronous adjustment of the illuminating light sheet and the objective lens used for fluorescence detection as well as by adaptation of a microfluidic system for application of fluorescent dyes, pharmaceutical agents or drugs in small quantities. A protocol for working with this system is given, and some technical details are reported. Representative results include (1) measurements of the uptake of a cytostatic drug (doxorubicin) and its partial conversion to a degradation product, (2) redox measurements by use of a genetically encoded glutathione sensor upon addition of an oxidizing agent, and (3) initiation and labeling of cell necrosis upon inhibition of the mitochondrial respiratory chain. Differences and advantages of the present SPIM module in comparison with existing systems are discussed.
引用
收藏
页数:10
相关论文
共 23 条
[1]  
Bruns T., 2013, European Patent Application EP, Patent No. [13 184 931.7, 13184931]
[2]   Preparation strategy and illumination of three-dimensional cell cultures in light sheet-based fluorescence microscopy [J].
Bruns, Thomas ;
Schickinger, Sarah ;
Wittig, Rainer ;
Schneckenburger, Herbert .
JOURNAL OF BIOMEDICAL OPTICS, 2012, 17 (10)
[3]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[4]   A line scanned light-sheet microscope with phase shaped self-reconstructing beams [J].
Fahrbach, Florian O. ;
Rohrbach, Alexander .
OPTICS EXPRESS, 2010, 18 (23) :24229-24244
[5]   Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination [J].
Gustafsson, Mats G. L. ;
Shao, Lin ;
Carlton, Peter M. ;
Wang, C. J. Rachel ;
Golubovskaya, Inna N. ;
Cande, W. Zacheus ;
Agard, David A. ;
Sedat, John W. .
BIOPHYSICAL JOURNAL, 2008, 94 (12) :4957-4970
[6]   Spectral analysis of doxorubicin accumulation and the indirect quantification of its DNA intercalation [J].
Hovorka, Ondrej ;
Subr, Vladimir ;
Vetvicka, David ;
Kovar, Lubomir ;
Strohalm, Jiri ;
Strohalm, Martin ;
Benda, Ales ;
Hof, Martin ;
Ulbrich, Karel ;
Rihova, Blanka .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2010, 76 (03) :514-524
[7]   Optical sectioning deep inside live embryos by selective plane illumination microscopy [J].
Huisken, J ;
Swoger, J ;
Del Bene, F ;
Wittbrodt, J ;
Stelzer, EHK .
SCIENCE, 2004, 305 (5686) :1007-1009
[8]   Selective plane illumination microscopy techniques in developmental biology [J].
Huisken, Jan ;
Stainier, Didier Y. R. .
DEVELOPMENT, 2009, 136 (12) :1963-1975
[9]   Multiphoton microscopy in life sciences [J].
König, K .
JOURNAL OF MICROSCOPY, 2000, 200 (02) :83-104
[10]   The use of 3-D cultures for high-throughput screening: The multicellular spheroid model [J].
Kunz-Schughart, LA ;
Freyer, JP ;
Hofstaedter, F ;
Ebner, R .
JOURNAL OF BIOMOLECULAR SCREENING, 2004, 9 (04) :273-285