Nerve Outgrowth Tracking

Nerve outgrowth tracking is a microscopy-based method for measuring how growing neurons extend neurites, the immature processes that can develop into axons and dendrites. By capturing cells over time and analyzing changes in neurite length, branching, direction, and growth-cone movement under defined culture conditions, researchers quantify the dynamics of neuronal development. In neuroscience, these measurements help evaluate guidance cues, genetic or pharmacological effects, injury responses, and regenerative strategies, while providing reproducible readouts for comparing experimental models and treatments.

Nerve Outgrowth Tracking - Related Videos

Research

JoVE Journal - Neuroscience

Organotypic Slice Culture of GFP-expressing Mouse Embryos for Real-time Imaging of Peripheral Nerve Outgrowth

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Cited by 5 •

2011

We present a method to prepare organotypic slices of mid-gestation mouse embryos for the cultivation and time-lapse imaging of peripheral nerve outgrowth.

Quantifying Yeast Chronological Life Span by Outgrowth of Aged Cells

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Cited by 91 •

2009

Chronological aging in yeast refers to the loss of cell viability associated with time in stationary phase. Here we describe a high-throughput method for quantitatively determining yeast chronological life span.

Immunofluorescence Assay to Evaluate Effect of Target Proteins on Neurite Outgrowth

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2025

In this video, we demonstrate an EGFP-based immunofluorescence assay to identify the efficacy of target proteins on the neurite outgrowth of primary cortical neurons. The primary neurons are transfected with a fluorescent protein, EGFP, and a target protein, and then an immunoassay is performed to investigate the effect of the target protein on neurite outgrowth.

Epicardial Outgrowth Culture Assay and Ex Vivo Assessment of Epicardial-derived Cell Migration

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Cited by 9 •

2016

Here, we describe methods for isolating primary mouse epicardial cells by an outgrowth culture assay and assessing the functional migration of epicardial-derived cells (EPDC) using an ex vivo heart culture system. These protocols are suitable for identifying genetic and chemical modulators of epicardial epithelial-to-mesenchymal transition (EMT) and motility.

Research

JoVE Journal - Neuroscience
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In Vivo Single-Molecule Tracking at the Drosophila Presynaptic Motor Nerve Terminal

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Cited by 14 •

2018

Here we illustrate how single molecule photo-activated localization microscopy can be carried out on the motor nerve terminal of a live Drosophila melanogaster third instar larva.

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