X-Ray Microscopy as an Approach to Increasing Accuracy and Efficiency of Serial Block-Face Imaging for Correlated Light and Electron Microscopy of Biological Specimens

被引:47
作者
Bushong, Eric A. [1 ]
Johnson, Donald D., Jr. [1 ]
Kim, Keun-Young [1 ]
Terada, Masako [2 ]
Hatori, Megumi [3 ]
Peltier, Steven T. [1 ]
Panda, Satchidananda [3 ]
Merkle, Arno [2 ]
Ellisman, Mark H. [1 ,4 ]
机构
[1] Univ Calif San Diego, Ctr Res Biol Syst, Natl Ctr Microscopy & Imaging Res, La Jolla, CA 92093 USA
[2] Carl Zeiss X Ray Microscopy Inc, Pleasanton, CA 94588 USA
[3] Salk Inst Biol Sci, La Jolla, CA 92037 USA
[4] Univ Calif San Diego, Dept Neurosci, Sch Med, La Jolla, CA 92093 USA
关键词
X-ray microscopy; microcomputed tomography; serial block-face scanning electron microscopy; correlative microscopy; upconverting nanoparticles; MODEL SYSTEM; TISSUE;
D O I
10.1017/S1431927614013579
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The recently developed three-dimensional electron microscopic (EM) method of serial block-face scanning electron microscopy (SBEM) has rapidly established itself as a powerful imaging approach. Volume EM imaging with this scanning electron microscopy (SEM) method requires intense staining of biological specimens with heavy metals to allow sufficient back-scatter electron signal and also to render specimens sufficiently conductive to control charging artifacts. These more extreme heavy metal staining protocols render specimens light opaque and make it much more difficult to track and identify regions of interest (ROIs) for the SBEM imaging process than for a typical thin section transmission electron microscopy correlative light and electron microscopy study. We present a strategy employing X-ray microscopy (XRM) both for tracking ROIs and for increasing the efficiency of the workflow used for typical projects undertaken with SBEM. XRM was found to reveal an impressive level of detail in tissue heavily stained for SBEM imaging, allowing for the identification of tissue landmarks that can be subsequently used to guide data collection in the SEM. Furthermore, specific labeling of individual cells using diaminobenzidine is detectable in XRM volumes. We demonstrate that tungsten carbide particles or upconverting nanophosphor particles can be used as fiducial markers to further increase the precision and efficiency of SBEM imaging.
引用
收藏
页码:231 / 238
页数:8
相关论文
共 25 条
[1]   Resolution of the three dimensional structure of components of the glomerular filtration barrier [J].
Arkill, Kenton P. ;
Qvortrup, Klaus ;
Starborg, Tobias ;
Mantell, Judith M. ;
Knupp, Carlo ;
Michel, C. Charles ;
Harper, Steve J. ;
Salmon, Andy Hj ;
Squire, John M. ;
Bates, Dave O. ;
Neal, Chris R. .
BMC NEPHROLOGY, 2014, 15
[2]   Correlated light and electron microscopy of the cytoskeleton [J].
Auinger, Sonja ;
Small, J. Victor .
INTRODUCTION TO ELECTRON MICROSCOPY FOR BIOLOGISTS, 2008, 88 :257-+
[3]   Correlative Tomography [J].
Burnett, T. L. ;
McDonald, S. A. ;
Gholinia, A. ;
Geurts, R. ;
Janus, M. ;
Slater, T. ;
Haigh, S. J. ;
Ornek, C. ;
Almuaili, F. ;
Engelberg, D. L. ;
Thompson, G. E. ;
Withers, P. J. .
SCIENTIFIC REPORTS, 2014, 4
[4]  
Deerinck T., 2010, Microscopy and Microanalysis, V16, P1138, DOI 10.1017/S1431927610055170
[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]   Time-Restricted Feeding without Reducing Caloric Intake Prevents Metabolic Diseases in Mice Fed a High-Fat Diet [J].
Hatori, Megumi ;
Vollmers, Christopher ;
Zarrinpar, Amir ;
DiTacchio, Luciano ;
Bushong, Eric A. ;
Gill, Shubhroz ;
Leblanc, Mathias ;
Chaix, Amandine ;
Joens, Matthew ;
Fitzpatrick, James A. J. ;
Ellisman, Mark H. ;
Panda, Satchidananda .
CELL METABOLISM, 2012, 15 (06) :848-860
[7]  
Helmstaedter M, 2013, NAT METHODS, V10, P501, DOI [10.1038/NMETH.2476, 10.1038/nmeth.2476]
[8]   3D Imaging of mammalian cells with ion-abrasion scanning electron microscopy [J].
Heymann, Jurgen A. W. ;
Shi, Dan ;
Kim, Sang ;
Bliss, Donald ;
Milne, Jacqueline L. S. ;
Subramaniam, Sriram .
JOURNAL OF STRUCTURAL BIOLOGY, 2009, 166 (01) :1-7
[9]   Synaptic Inputs Compete during Rapid Formation of the Calyx of Held: A New Model System for Neural Development [J].
Holcomb, Paul S. ;
Hoffpauir, Brian K. ;
Hoyson, Mitchell C. ;
Jackson, Dakota R. ;
Deerinck, Thomas J. ;
Marrs, Glenn S. ;
Dehoff, Marlin ;
Wu, Jonathan ;
Ellisman, Mark H. ;
Spirou, George A. .
JOURNAL OF NEUROSCIENCE, 2013, 33 (32) :12954-12969
[10]   Large-Scale Automated Histology in the Pursuit of Connectomes [J].
Kleinfeld, David ;
Bharioke, Arjun ;
Blinder, Pablo ;
Bock, Davi D. ;
Briggman, Kevin L. ;
Chklovskii, Dmitri B. ;
Denk, Winfried ;
Helmstaedter, Moritz ;
Kaufhold, John P. ;
Lee, Wei-Chung Allen ;
Meyer, Hanno S. ;
Micheva, Kristina D. ;
Oberlaender, Marcel ;
Prohaska, Steffen ;
Reid, R. Clay ;
Smith, Stephen J. ;
Takemura, Shinya ;
Tsai, Philbert S. ;
Sakmann, Bert .
JOURNAL OF NEUROSCIENCE, 2011, 31 (45) :16125-16138