Ex vivo Culture of Mouse Embryonic Skin and Live-imaging of Melanoblast Migration

Summary

We describe the dissection and ex vivo culture of mouse embryonic skin. The culture system maintains an air-liquid interface across the tissue surface and allows imaging on an inverted microscope. Melanoblasts, a component of the developing skin, are fluorescently labeled allowing their behavior to be observed using confocal microscopy.

Abstract

Melanoblasts are the neural crest derived precursors of melanocytes; the cells responsible for producing the pigment in skin and hair. Melanoblasts migrate through the epidermis of the embryo where they subsequently colonize the developing hair follicles^1,2. Neural crest cell migration is extensively studied in vitro but in vivo methods are still not well developed, especially in mammalian systems. One alternative is to use ex vivo organotypic culture^3-6. Culture of mouse embryonic skin requires the maintenance of an air-liquid interface (ALI) across the surface of the tissue^3,6. High resolution live-imaging of mouse embryonic skin has been hampered by the lack of a good method that not only maintains this ALI but also allows the culture to be inverted and therefore compatible with short working distance objective lenses and most confocal microscopes. This article describes recent improvements to a method that uses a gas permeable membrane to overcome these problems and allow high-resolution confocal imaging of embryonic skin in ex vivo culture⁶. By using a melanoblast specific Cre-recombinase expressing mouse line combined with the R26YFPR reporter line we are able to fluorescently label the melanoblast population within these skin cultures. The technique allows live-imaging of melanoblasts and observation of their behavior and interactions with the tissue in which they develop. Representative results are included to demonstrate the capability to live-image 6 cultures in parallel.

Introduction

Traditionally embryonic skin has been cultured by dissecting from the mouse embryo and mounting on a polycarbonate Nuclepore membrane. The membrane is then floated on culture medium, thus maintaining an air-liquid interface across the surface of the developing tissue^3,4. This technique has been used to assay melanoblast behavior by fixing the tissue and assessing melanoblast distribution using β-galactosidase as a marker⁷. We have developed a method that allows live-imaging of fluorescently labeled melanoblasts in ex vivo skin culture⁶. Here we describe the method in detail from dissection, to setup, to live confocal imaging and include some recent improvements.

Melanoblasts are the embryonic precursors of melanocytes, the cells that produce pigment in hair and skin. Melanoblasts arise in the neural crest adjacent to the neural tube at around embryonic day 9 (E9) in the developing mouse embryo. Subsequently they migrate along a dorsolateral pathway between the ectoderm and the developing somites. At E12.5 they move from the dermis to the epidermis where they proliferate and continue their migration. The primary hair follicle pattern begins to form in the epidermis at E14.5 and by E15.5 melanoblasts are localizing to these follicles. For a review of melanoblast/melanocyte development see Thomas & Erickson (2008)¹. In order to label the melanoblast population we have combined Tyr::CreB animals that express Cre-recombinase driven by the mouse tyrosinase promoter⁸ with R26YFPR animals that express yellow fluorescent protein (YFP) conditionally from the ROSA26 locus⁹.

We describe a method to culture embryonic skin and capture images using an inverted confocal microscope. It is adapted form the original method described in Mort et al. (2010)⁶. The present method allows imaging in a 6-well format and removes the reliance on Nuclepore membranes and on matrigel to support the culture. Instead using a small block of 1% agarose to stabilize the embryonic skin. Removing the reliance on matrigel is important especially in situations where the response of the embryonic skin to soluble growth factors is the focus of study. Our original method has already been used to gain new insights into melanoblast development^10-13 and we anticipate that the improvements we describe here will make it more powerful as an experimental technique especially where multiple parallel cultures are a requirement.

Protocol

All animal work was performed in accordance with institutional guidelines under license by the UK Home Office (project license number PPL 60/3785 and 60/4424).

1. Preparation

1. Label the melanoblasts in the developing skin by combining an appropriate Cre-recombinase expressing mouse line with a fluorescent reporter mouse line. Tyr::CreA, Tyr::CreB⁸ and Wnt1::Cre¹⁴ have been used successfully as Cre-expressing lines and R26YFPR⁹ as a reporter line.
2. Prepare the culture medium in a laminar flow hood; supplement Dulbecco's Modified Eagle Medium (DMEM) with (1% v/v Penicillin/Streptomycin), 10% v/v fetal calf serum and 0.584 gm/L L-glutamine.
3. The live imaging apparatus is outlined in Figure 1 Sterilize the imaging chamber base by wiping down with 70% ethanol. Sterilize the inserts, imaging clips, and O-rings by soaking overnight in 70% ethanol. Use a sterile lid from a 6-well plate as the lid of the chamber.
4. The bottom surface of the imaging chamber consists of a lummox membrane held in place by an O-ring (Figure 1). Start with a 35 mm gas permeable lummox dish. Place the dish over the imaging chamber and cut out the gas permeable membrane with a single edged razor blade. Push the O-ring over the membrane to secure it to the imaging chamber.
5. The imaging clips (6 in total) clamp the embryonic skin in place (Figure 1) before use they must be filled with 1% agarose. Prepare a 2% solution of agarose with sterile dH₂O by microwaving and cooling to 60 °C. Mix 1:1 with 10 ml culture medium (see step 2) preheated to 60 °C. Stand the 6 imaging clips in a sterile 6-well plate. Drip the 1% agarose solution into the center of each clip using a fine pastette and allow to cool. Add 1 ml cold sterile PBS to each well to prevent the agarose from drying out. The imaging clips can be stored for several hours in PBS.
6. To carry out the delicate separation of embryonic skin and to handle the dissected tissue use the 'hair stick method' as described in Kashiwagi et al.³ Instead of using a chopstick a bamboo kebab skewer can be used. Make a small slit in the flat end of the skewer using a single edged razor blade and insert a soft toothbrush bristle. Trim the skewer so that it is approximately 15 cm in length.
7. Use a confocal microscope with a full environmental chamber or stage top chamber providing 5% CO₂ in air. Prewarm the microscope stage to 37 °C for at least 1 hr prior to imaging. This helps to prevent sample drift caused by expansion of the stage components as they warm up.
8. Prepare a multi-position set using the microscope's control software so that one can quickly and easily center on the middle of each culture to set up an experiment.

2. Procedure

1. Mate the mice and designate the first day post coitum as day E0.5. At day E14.5, cull the female by cervical dislocation and expose the body cavity by making a small midline incision, pulling apart the skin towards the head and tail and then cutting the underlying peritoneum and pealing back to either side of the body. Dissect the uterus into cold sterile PBS by holding firmly with forceps and snipping along the mesometrium using surgical scissors. Keep the uterus on ice until required. For a detailed description see Shea et al. (2007)¹⁵.
2. Dissect embryos from the uterus by first cutting the length of the uterine wall with surgical scissors to release the decidua and then dissecting the embryos from the decidua by pulling them apart with two pairs of fine forceps. Screen for fluorescent reporter expression (if necessary).
3. Cull embryos by decapitation prior to dissection. Subsequently remove the tail and hind limbs and then the forelimbs using a single edged razor blade. Retain tissue for genotyping if required.
4. Make an incision in the ventrum close to the midline in a rostro-caudal direction. Using the hair sticks described in step 1.6, carefully tease away the skin from the underlying connective tissue rotating the embryo at the same time. Do not remove the skin completely but rather leave it attached along the ventral edge furthest from the first incision.
5. It is important not to let the skin become screwed up as it is then very difficult to mount. To prevent this, flatten out the skin using the hair sticks (dermal side up) on the surface of a dry Petri dish and then cut away from the embryo trunk using a single edged razor blade. The dermal side can be distinguished from the epidermal side by careful observation of the junction between the dissected tissue and the embryo before the skin is removed. The area of the dissected tissue is approximately 0.5 mm² when dissecting an E14.5 embryo.
6. Place an imaging clip on top of the skin so that the agarose is touching the dermal side of the tissue. Allow to stand for 60 sec and then carefully tease the edges of the tissue up the sides of the clip. Invert the clip and use the hair sticks to flatten out the skin and remove any air bubbles, taking care to touch the surface of the tissue (in the area that will be imaged) as little as possible.
7. Use silk suture thread to tie the skin to the imaging clip using two simple thumb knots on either side of the imaging clip so that they tighten and pull the skin into the groove close to the top of the clip. Invert the clip, push inside the imaging insert and place in the base. Fill the insert with ~5 ml of culture medium (see step 1.2). Figure 1 outlines the assembly of the imaging chamber.
8. Repeat Protocol for the remaining 5 samples.

3. Live Imaging

1. The imaging chamber has the same dimensions as a standard 6-well plate. Use an appropriate plate insert to mount the chamber on the stage of the confocal microscope.
2. An automated stage is required to image the cultures in parallel. Define the six positions to image in the confocal software. The exact settings will depend on the capability of the microscope used. Typically a small z-stack (3-5 z-positions to account for any stage drift) is used in each of the 6-positions and a z-stack is captured every 2 min for 18-24 hr. For live-imaging applications it is generally advantageous to use a wider than optically optimal pinhole setting to reduce laser power and the number of z-sections required.

Results

Figure 2 shows representative results from a time lapse experiment using embryonic skin from Tyr::CreB x R26YFPR embryos at E14.5. 6 embryonic skin cultures were imaged by confocal microscopy every 2 min for 18 hr. The freeware image analysis software package ImageJ was used to analyze the behavior of the YFP-labeled melanoblasts in the 6 movies. The melanoblasts were automatically tracked using the wrMTrck plugin developed by Jesper Søndergaard Pedersen (

Discussion

We describe a method to culture embryonic skin that is particularity amenable to live-cell imaging on inverted confocal microscopes. The method includes recent improvements that allow 6 cultures to be imaged in parallel and removes the reliance on matrigel and Nuclepore membranes of the original method⁶. The crucial technical difference from similar techniques is the use of a gas-permeable lummox membrane to establish an air liquid interface and also to act as a coverslip. We have successfully maintained the c...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
DMEM high glucose	Biochrom AG	F0475	without phenol red
Penicillin	Sigma	P3032
Streptomycin	Sigma	S9137
Fetal calf serum	Hyclone	SV30160.03
Glutamax	Gibco	35050-038
Ethanol	Generic
Live imaging chamber	Custom made
Lummox dishes	Sarstedt	94.6077.410
6-well plate	Greiner Bio-One	657-160
Single edged razor blade	Fisher Scientific	1244-3170
Agarose	Biogene	300-300
Fine pastette	Generic
PBS	Generic
Kebab skewers	Waitrose		Bamboo BBQ skewers 30 cm
Toothbrush	Generic
Petri dishes	Greiner Bio-One	633185
Suture thread	Look	SP115	Black silk suture thread