Advantages of indium-tin oxide-coated glass slides in correlative scanning electron microscopy applications of uncoated cultured cells

被引:37
作者
Pluk, H. [1 ]
Stokes, D. J. [2 ]
Lich, B. [2 ]
Wieringa, B. [1 ]
Fransen, J. [1 ]
机构
[1] Radford Univ, Nijmegen Ctr Mol Life Sci, Dept Cell Biol, Nijmegen Med Ctr, NL-6500 HB Nijmegen, Netherlands
[2] FEI Co, NL-5600 KA Eindhoven, Netherlands
关键词
Backscattered electron imaging; conductive glass slides; correlative microscopy; fluorescence light microscopy; indium-tin oxide; mouse embryonic fibroblasts; scanning electron microscopy; ADHERENT CELLS; SUCRASE-ISOMALTASE; ELECTROPORATION; ESEM; ULTRASTRUCTURE; EXPRESSION; STRATEGIES; MORPHOLOGY; GROWTH; GOLD;
D O I
10.1111/j.1365-2818.2009.03140.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
A method of direct visualization by correlative scanning electron microscopy (SEM) and fluorescence light microscopy of cell structures of tissue cultured cells grown on conductive glass slides is described. We show that by growing cells on indium-tin oxide (ITO)-coated glass slides, secondary electron (SE) and backscatter electron (BSE) images of uncoated cells can be obtained in high-vacuum SEM without charging artefacts. Interestingly, we observed that BSE imaging is influenced by both accelerating voltage and ITO coating thickness. By combining SE and BSE imaging with fluorescence light microscopy imaging, we were able to reveal detailed features of actin cytoskeletal and mitochondrial structures in mouse embryonic fibroblasts. We propose that the application of ITO glass as a substrate for cell culture can easily be extended and offers new opportunities for correlative light and electron microscopy studies of adherently growing cells.
引用
收藏
页码:353 / 363
页数:11
相关论文
共 49 条
[1]  
Boyes ED, 2000, MICROSC MICROANAL, V6, P307
[2]   Contribution of high-resolution correlative imaging techniques in the study of the liver sieve in three-dimensions [J].
Braet, Filip ;
Wisse, Eddie ;
Bomans, Paul ;
Frederik, Peter ;
Geerts, Willie ;
Koster, Abraham ;
Soon, Lilian ;
Ringer, Simon .
MICROSCOPY RESEARCH AND TECHNIQUE, 2007, 70 (03) :230-242
[3]   Recent developments and new strategies in scanning electron microscopy [J].
Cazaux, J .
JOURNAL OF MICROSCOPY, 2005, 217 :16-35
[4]   Role of target geometry in phagocytosis [J].
Champion, JA ;
Mitragotri, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (13) :4930-4934
[5]   Serial block-face scanning electron microscopy to reconstruct three-dimensional tissue nanostructure [J].
Denk, W ;
Horstmann, H .
PLOS BIOLOGY, 2004, 2 (11) :1900-1909
[6]   The use of environmental scanning electron microscopy for imaging wet and insulating materials [J].
Donald, AM .
NATURE MATERIALS, 2003, 2 (08) :511-516
[7]   CASINO V2.42 - A fast and easy-to-use modeling tool for scanning electron microscopy and microanalysis users [J].
Drouin, Dominique ;
Couture, Alexandre Real ;
Joly, Dany ;
Tastet, Xavier ;
Aimez, Vincent ;
Gauvin, Raynald .
SCANNING, 2007, 29 (03) :92-101
[8]   High-resolution backscatter electron imaging of colloidal gold in LVSEM [J].
Erlandsen, S ;
Chen, Y ;
Frethem, C ;
Detry, J ;
Wells, C .
JOURNAL OF MICROSCOPY-OXFORD, 2003, 211 :212-218
[9]   Strategies for low- and very-low-energy SEM [J].
Frank, L ;
Müllerová, I .
JOURNAL OF ELECTRON MICROSCOPY, 1999, 48 (03) :205-219
[10]  
Gobbi P, 2000, SCANNING, V22, P273, DOI 10.1002/sca.4950220501