3D Imaging of mammalian cells with ion-abrasion scanning electron microscopy

被引:82
|
作者
Heymann, Jurgen A. W. [1 ]
Shi, Dan [1 ]
Kim, Sang [1 ]
Bliss, Donald [1 ]
Milne, Jacqueline L. S. [1 ]
Subramaniam, Sriram [1 ]
机构
[1] NCI, Cell Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
关键词
Automated 3D imaging; Melanoma detection; Mitochondrial architecture; Dual beam microscopy; Cancer imaging; CRYOELECTRON MICROSCOPY; ENDOPLASMIC-RETICULUM; MITOCHONDRIA; TOMOGRAPHY; VISUALIZATION; MELANOSOMES; SPECIMENS;
D O I
10.1016/j.jsb.2008.11.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding the hierarchical organization of molecules and organelles within the interior of large eukaryotic cells is a challenge of fundamental interest in cell biology. We are using ion-abrasion scanning electron microscopy (IA-SEM) to visualize this hierarchical organization in an approach that combines focused ion-beam milling with scanning electron microscopy. Here, we extend our previous studies on imaging yeast cells to image subcellular architecture in human melanoma cells and melanocytes at resolutions as high as similar to 6 and similar to 20 nm in the directions parallel and perpendicular, respectively, to the direction of ion-beam milling. The 3D images demonstrate the striking spatial relationships between specific organelles such as mitochondria and membranes of the endoplasmic reticulum, and the distribution of unique cellular components such as melanosomes. We also show that 10 nm-sized gold particles and quantum dot particles with 7 nm-sized cores can be detected in single cross-sectional images. IA-SEM is thus a useful tool for imaging large mammalian cells in their entirety at resolutions in the nanometer range. Published by Elsevier Inc.
引用
收藏
页码:1 / 7
页数:7
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