Serial Slicing Imaging

Serial slicing imaging is a technique that combines sequentially sectioning biological tissue with image acquisition to visualize structures across multiple planes and reconstruct their three-dimensional organization. In neuroscience, a brain or neural tissue sample is cut into a series of thin, ordered sections; each section is stained or labeled, imaged, and computationally aligned so corresponding cells, fibers, or anatomical regions can be traced through the volume. This approach supports quantitative mapping of neural circuits, cell distributions, and tissue architecture, linking microscopic observations to larger brain structures. It is valuable for studying development, disease-related changes, connectivity, and the organization of complex nervous systems.

Serial Slicing Imaging - Related Videos

Research

JoVE EoE - Neuroimaging

Imaging of Neuronal Mitochondria Using a Serial Block-Face Scanning Electron Microscope

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2025

Source: Mukherjee, K., et. al. Analysis of Brain Mitochondria Using Serial Block-Face Scanning Electron Microscopy. J. Vis. Exp. (2016)This video demonstrates the preparation, imaging, and analysis of mouse brain tissue using a serial block-face scanning electron microscope (SBFSEM) to visualize mitochondrial ultrastructure, enabling precise mapping of their morphology and spatial distribution in axonal and dendritic neuronal compartments.

A Rapid Approach to High-Resolution Fluorescence Imaging in Semi-Thick Brain Slices

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Cited by 10 •

2011

Here we describe a rapid and simple method to image fluorescently labeled cells in semi-thick brain slices. By fixing, slicing, and optically clearing brain tissue we describe how standard epifluorescent or confocal imaging can be used to visualize individual cells and neuronal networks within intact nervous tissue.

Preparation of Acute Subventricular Zone Slices for Calcium Imaging

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Cited by 2 •

2012

A method to load subventricular zone (SVZ) cells with calcium indicator dyes for recording calcium activity is described. The postnatal SVZ contains tightly packed cells including neural progenitor cells and neuroblasts. Rather than using bath loading we injected the dye by pressure inside the tissue allowing better dye diffusion.

Ex Vivo Culture and Imaging of Oculomotor Slices from Transgenic Mouse Embryos

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2025

This video demonstrates the ex vivo culture and imaging of oculomotor slices from transgenic mouse embryos. The embryos are isolated and embedded in agarose. Using a vibratome, slices containing the oculomotor nuclei and eyes are obtained. The slices are maintained in culture and imaged using a fluorescence microscope.

Research

JoVE Journal - Bioengineering
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Quantifying Intermembrane Distances with Serial Image Dilations

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Cited by 12 •

2018

The purpose of this algorithm is to continuously measure the distance between two 2-dimensional edges using serial image dilations and pathfinding. This algorithm can be applied to a variety of fields such as cardiac structural biology, vascular biology, and civil engineering.

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