Comparative three-dimensional imaging of living neurons with confocal and atomic force microscopy

被引:31
作者
McNally, HA [1 ]
Rajwa, B
Sturgis, J
Robinson, JP
机构
[1] Purdue Univ, Sch Vet Med, Ctr Paralysis Res, W Lafayette, IN 47906 USA
[2] Purdue Univ, Sch Vet Med, Cytometry Labs, W Lafayette, IN 47907 USA
[3] Purdue Univ, Sch Engn, Dept Biomed Engn, W Lafayette, IN 47907 USA
关键词
atomic force microscopy; confocal laser scanning microscopy; neurogenesis; neurotrauma; neurobiology;
D O I
10.1016/j.jneumeth.2004.08.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Atomic force microscopy applications extend across a number of fields; however, limitations have reduced its effectiveness in live cell analysis. This report discusses the use of AFM to evaluate the three-dimensional (3-D) architecture of living chick dorsal root ganglia and sympathetic ganglia. These data sets were compared to similar images acquired with confocal laser scanning microscopy of identical cells. For this comparison we made use of visualization techniques which were applicable to both sets of data and identified several issues when coupling these technologies. These direct comparisons offer quantitative validation and confirmation of the character of novel images acquired by AFM. This paper is one in a series emphasizing various new applications of AFM in neurobiology. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
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