Neural Explant Method

The neural explant method is an ex vivo technique in which small pieces of nervous tissue are isolated and maintained in culture to study neural development and function under controlled conditions. After dissection, the tissue is placed on a suitable substrate or in culture medium, allowing neurons and supporting cells to survive, extend processes, and respond to defined experimental conditions while preserving aspects of their local organization. Researchers use neural explants to examine axon growth, cell migration, connectivity, and responses to molecular or physical cues. This approach links cellular mechanisms with tissue-level behavior and supports studies of nervous system development, injury, and regeneration.

Neural Explant Method - Related Videos

Education

JoVE Science Education - Advanced Biology

Explant Culture of Neural Tissue

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2023

The intricate structure of the vertebrate nervous system arises from a complex series of events involving cell differentiation, cell migration, and changes in cell morphology. Studying these processes is essential to our understanding of nervous system function as well as our ability to diagnose and treat disorders that result from abnormal development. However, neural tissues are relatively inaccessible for experimental manipulations, especially in embryonic mammals. As a result, many...

Research

JoVE Journal - Neuroscience

Neural Explant Cultures from Xenopus laevis

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Cited by 23 •

2012

Culturing neural explants from dissected Xenopus laevis embryos that express fluorescent fusion proteins allows for imaging of growth cone cytoskeletal dynamics.

Stem cell-like Xenopus Embryonic Explants to Study Early Neural Developmental Features In Vitro and In Vivo

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Cited by 1 •

2016

In Xenopus embryos, cells from the roof of the blastocoel are pluripotent and can be programmed to generate various tissues. Here, we describe protocols to use amphibian blastocoel roof explants as an assay system to investigate key in vivo and in vitro features of early neural development.

Dissection of Xenopus laevis Neural Crest for in vitro Explant Culture or in vivo Transplantation

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Cited by 22 •

2014

This protocol describes how to dissect premigratory cranial neural crest (NC) from Xenopus laevis neurulas. These explants can be plated on fibronectin and cultured in vitro, or grafted back into host embryos. This technique allows studying the mechanisms of NC epithelium-to-mesenchyme transition, migration, and differentiation.

Analyzing Neural Stem Cell Reactivation in Cultured Drosophila Brain Explants

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2025

This video demonstrates a protocol to identify exogenous factors that initiate the reactivation of Drosophila brain neural stem cells from their quiescent state. Freshly hatched larvae are dissected to isolate their brains, which are then cultured in media with or without a test hormone to evaluate the hormone's potential to induce neural stem cell reactivation and proliferation.

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