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Method Article

Isolating Cranial Neural Folds From a Chick Embryo for a Neural Crest Cell Culture

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July 8th, 2025

In This Article

Abstract

Source: Jacques-Fricke, B. T., et al. Preparation and Morphological Analysis of Chick Cranial Neural Crest Cell Cultures. J. Vis. Exp. (2022).

This video illustrates a technique for isolating cranial neural folds from the midbrain region of chick embryos. It presents a detailed dissection process of the neural folds, their placement, and attachment on fibronectin-coated coverslips, followed by the observation of neural crest cell migration from the neural folds.

Protocol

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.

1. Preparation of solutions and materials

  1. Prepare Ringer's solution by mixing 123.3 mM NaCl, 1.53 mM CaCl2, 4.96 mM KCl, 0.809 mM Na2HPO4, and 0.147 mM KH2PO4 (see Table of Materials). Adjust pH to 7.4 and filter sterilize into 100 mL bottles. Store in a clean, dry location. Do not wash bottles with soap (treat as tissue culture glassware).
  2. Prepare 1 mg/mL stock solution fibronectin (FN) (....

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Results

Developmental biology experiment; microscope images of embryo tissues, segmentation and analysis.
Figure 1. Dissection of chick dorsal neural folds. Working in Ringer's P/S, spring scissors were used to excise neural folds. (A) Embryo dorsal view, anterior toward the top of the figure. Neural folds appear more opaque than the surroundi.......

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Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
AxioObserver equipped with an LSM710 confocal scan head controlled by ZEN 3.0 SR softwareZeissUsed alpha Plan-Apochromat 100x/1.46 Oil DIC M27 objective
CaCl2Sigma-AldrichC3306
Chamber dishes (glass bottom, single or divided)MatTek; Cell VisP35G-1.5-14-C (MatTek)
X000NOJQGX (Cellvis) X000NOK1OJ (Cellvis)
Single chamber 35 mm or 4 chamber 35 mm
Cover glassCarolina Biological Supply Company633029, 633031, 633033, 633035,
633037
circles, 0.13–0.17 mm thickness, available in 12-25 mm diameter
DMEM/F12ThermoFisher Scientific11320033Alternative for L15 media
Egg incubatorSportsman1502
FBSLife Technologies10437-028
FibronectinFisher ScientificCB-40008A
Filter paperWhatmangrade 3MM chromatography
Forceps (blunt)Fisher Scientific; Thomas Scientific08-890 (Fisher);1141W97 (Thomas)
Forceps (fine)Fine Science Tools11252-20Dumont #5
Pin holder Fine Science Tools26016-12For tungsten needle (alternative for spring scissors)
KClSigma-AldrichP3911
KH2PO4Sigma-AldrichP0662
L15 mediaInvitrogen11415064
L-glutamineInvitrogen25030
Na2HPO4Sigma-AldrichS9638
NaClSigma-AldrichS9888
Penicillin/streptomycinLife Technologies15140-14810,000 Units/mL Penicillin; 10,000 mg/mL Streptomycin
Petri DishesVWR (or similar)60 mm, 100 mm
Scissors (dissection)Fine Science Tools14061-10
Spring ScissorsFine Science Tools15000-082.5 mm cutting edge (alternative for tungsten needle)
SylgardKraydenSylgard 184
Syringe FiltersSigma-AldrichSLGVM33RSMillex-GV Syringe Filter Unit, 0.22 µm, PVDF, 33 mm, gamma sterilized
Tissue culture dishesSarstedt83-390035 mm culture dishes for bulk neural fold cultures
Tungsten wireVariety of sources0.01" diameter for tungsten needle (alternative for spring scissors)

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