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Updated: Jan 30, 2026

Imaging Neurons within Thick Brain Sections Using the Golgi-Cox Method
Published on: April 18, 2017
Modernization of Golgi staining techniques for high-resolution, 3-dimensional imaging of individual neurons
Katlijn Vints1,2, Dorien Vandael1,2, Pieter Baatsen1,2
1VIB-KU Leuven Center for Brain & Disease Research, Electron Microscopy Platform & VIB-Bioimaging Core, O&N4 Herestraat 49 box 602, 3000, Leuven, Belgium.
Abstract:
Analysis of neuronal arborization and connections is a powerful tool in fundamental and clinical neuroscience. Changes in neuronal morphology are central to brain development and plasticity and are associated with numerous diseases. Golgi staining is a classical technique based on a deposition of metal precipitate in a random set of neurons. Despite their versatility, Golgi methods have limitations that largely precluded their use in advanced microscopy. We combined Golgi staining with fluorescent labeling and tissue clearing techniques in an Alzheimer's disease model. We further applied 3D electron microscopy to visualize entire Golgi-stained neurons, while preserving ultrastructural details of stained cells, optimized Golgi staining for use with block-face scanning electron microscopy, and developed an algorithm for semi-automated neuronal tracing of cells displaying complex staining patterns. Our method will find use in fundamental neuroscience and the study of neuronal morphology in disease.
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