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Updated: Aug 10, 2026

Visualization of Endosome Dynamics in Living Nerve Terminals with Four-dimensional Fluorescence Imaging
Published on: April 16, 2014
Comparative three-dimensional imaging of living neurons with confocal and atomic force microscopy
Helen A McNally1, Bartek Rajwa, Jennie Sturgis
1Center for Paralysis Research, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47906-2065, USA. mcnallyh@purdue.edu
Abstract:
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.
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