Visualization of the nucleus and nuclear envelope in situ by SEM in tissue culture cells

被引:14
作者
Allen, T. D. [1 ]
Rutherford, S. A. [1 ]
Murray, S. [1 ]
Gardiner, F. [1 ]
Kiseleva, E. [2 ]
Goldberg, M. W. [3 ]
Drummond, S. P. [1 ]
机构
[1] Univ Manchester, Paterson Inst Canc Res, Manchester M20 4BX, Lancs, England
[2] Russian Acad Sci, Inst Cytol & Genet, Novosibirsk, Russia
[3] Univ Durham, Sch Biol & Biomed Sci, Durham DH1 3LE, England
关键词
D O I
10.1038/nprot.2007.139
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Our previous work characterizing the biogenesis and structural integrity of the nuclear envelope and nuclear pore complexes ( NPCs) has been based on amphibian material but has recently progressed into the analysis of tissue-culture cells. This protocol describes methods for the high resolution visualization, by field-emission scanning electron microscopy ( FESEM), of the nucleus and associated structures in tissue culture cells. Imaging by fluorescence light microscopy shows general nuclear and NPC information at a resolution of approximately 200 nm, in contrast to the 3-5 nm resolution provided by FESEM or transmission electron microscopy ( TEM), which generates detail at the macromolecular level. The protocols described here are applicable to all tissue culture cell lines tested to date ( HeLa, A6, DLD, XTC and NIH 3T3). The processed cells can be stored long term under vacuum. The protocol can be completed in 5 d, including 3 d for cell growth, 1 d for processing and 1 d for imaging.
引用
收藏
页码:1180 / 1184
页数:5
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