Drg Explant Culture

Dorsal root ganglion (DRG) explant culture is an ex vivo method that maintains sensory neuron tissue outside the organism to study neuronal survival and growth. In this approach, DRGs are carefully dissected, placed in a controlled culture environment, and monitored as sensory neurons extend neurites from the explanted tissue in response to experimental conditions. The model provides a useful bridge between isolated cell assays and whole-animal studies, supporting research on axon regeneration, neural development, injury responses, and neurotoxicity. Because it preserves interactions among neurons and associated ganglion cells, DRG explants can reveal how substrates, molecules, or treatments influence sensory neurite outgrowth.

Drg Explant Culture - Related Videos

Research

JoVE EoE - Neuronal Culture Techniques

Generating Dorsal Root Ganglion Explant and Dissociated Cell Culture

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2025

This video demonstrates a method to develop dorsal root ganglia or DRG explant culture and DRG-dissociated cell models using isolated mouse DRG tissues. These models help to study various mechanisms with neuron-glial interactions in a controlled environment.

Co-culturing of a Dorsal Root Ganglion Explant with Schwann Cells for Neuron Myelination

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2025

This video demonstrates the coculturing model of a dorsal root ganglion explant and Schwann cells. In coculture conditions, ascorbic acid promotes the differentiation of Schwann cells into myelinating forms. Myelinating Schwann cells wrap the axons multiple times to create a myelin sheath, which is essential for nerve function.

Co-Culture of Schwann Cells with DRG Neurons on a Pre-Stretched Membrane

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2025

The video demonstrates the co-culturing of dorsal root ganglion (DRG) neurons with Schwann cells. DRG neurons are first grown on a pre-stretched membrane for aligned axon growth. Schwann cells are then introduced, which attach to the axons, insulating them and promoting neural cell survival and function.

A Functional Motor Unit in the Culture Dish: Co-culture of Spinal Cord Explants and Muscle Cells

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Cited by 16 •

2012

Cultured muscle cells are an inadequate model to recapitulate innervated muscle in vivo. A functional motor unit can be reproduced in vitro by innervation of differentiated human primary muscle cells using rat embryo spinal cord explants. This article describes how co-cultures of spinal cord explants and muscle cells are established.

Education

JoVE Science Education - Advanced Biology

Explant Culture for Developmental Studies

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2023

Explant culture is a technique in which living cells or tissues are removed from an embryo for continued development outside of the organism. This ex vivo approach allows researchers to manipulate and observe developing tissues in ways that are not possible in vivo. Once established, explant culture is frequently used to understand the role of genes and signaling molecules in organogenesis. This video will first introduce the basic principles of explant culture and demonstrate a protocol to...

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