In ovo Expression of MicroRNA in Ventral Chick Midbrain

Summary

Ectopic expression is one technique to elucidate the microRNAs role in brain development. However, targeting specific areas using in ovo electroporation is challenging. Here, we show an efficient way to selectively electroporate ventral and dorsal midbrain regions.

Abstract

Non-coding RNAs are additional players in regulating gene expression. Targeted in ovo electroporation of specific areas provides a unique tool for spatial and temporal control of ectopic microRNA expression. However, ventral brain structures like ventral midbrain are rather difficult to reach for any manipulations. Here, we demonstrate an efficient way to electroporate miRNA into ventral midbrain using thin platinum electrodes. This method offers a reliable way to transfect specific areas of the midbrain and a useful tool for in vivo studies.

Introduction

The recognition of small non-coding RNAs as additional players for gene expression launched a new complexity to genomic programming/gene regulation. Different species of non-coding RNAs have functional importance in neural cells, including small non-coding RNAs^1-4. MicroRNAs (miR or miRNA) for example show distinct and changing expression profiles in developing brains⁵. Targeted in ovo electroporation of chick embryos provides a unique opportunity for temporal and spatial control of gene expression and silencing during development.

This video demonstrates the different steps of performing ectopic expression of miRs in specific areas of the chick midbrain using in ovo electroporation^6-10. To ensure a long lasting effect of these small non-coding RNAs in cells, the DNA sequence of miRs were cloned into mono- or bi-cistronic vectors. For in ovo electroporation, miR containing vector is injected into the midbrain neural tube by exposing the embryo after making a small window in the egg shell. To transfect specific areas of the midbrain small plus (anode) and minus (cathode) platinum electrodes are placed at specific positions. For ventral midbrain transfection, the anode is placed underneath the left ventral midbrain and the cathode above the right half of the midbrain before applying a current. The opening in the eggshell is closed with tape and embryos are incubated for as long as required for any analysis. This method was originally described by Muramatsu et al.⁶ and improved by Momose et al.⁸ for specific area transfection.

Schematic Overview.

1. The embryo in the egg is exposed by cutting a small window into the eggshell.
2. The dissolved vector(s) is injected into the midbrain using a micro capillary.
3. Two electrodes - placed parallel or under and above the embryo - generate a pulsed electric field.
4. The electric field temporally creates pores in the cell membrane, which facilitate entry into the cell by the negatively charged DNA (or RNA) attracted to the anode^11,12.

Protocol

1. Requirements for In ovo Electroporation

1. Preparing the vector construct: miR sense and antisense primers were designed after the instructions of Ambion, annealed and ligated into ApaI/EcoRI digested pSilencer U6.1 vector. After successful transformation one of the resulting clones was grown and pSilencer plasmid was isolated by alkaline lysis method using a Quiagen midi preparation kit.
2. Electrodes: Electrodes can be purchased or easily be built¹³. We use self-made electrodes of platinum wire (Φ = 0.2, 0.25, or 0.5 mm in diameter) or in some cases an even smaller tungsten wire electrode (Φ = 0.1 mm)⁸ depending on which area we want to electroporate. To avoid scorching of tissue, we use as a rule the nearer to the tissue the thinner the electrodes. For broad electroporation of midbrain, we use 0.5 mm platinum wires soldered to a brass/stainless steel tubular shaft and fixed to an electrode holder with a distance of 3-5 mm (Figure 1). To electroporate specific areas, we use 0.25 mm platinum wire anodes and 0.2 mm platinum wire or 0.1 mm tungsten for the cathode with an approximate distance of 1 mm or less.
3. Solutions: Have the following solutions ready:
   1. Autoclaved chicken Ringer, pH 7.5 (9.0 g NaCl, 0.42 g KCl, 0.24 g CaCl2, dissolve in 1 L distilled water).
   2. PBS (8 g NaCl, 0.2 g KCl, 0.24 g KH₂PO4, 1.44 g Na₂HPO₄, dissolve in 1l distilled H₂O).
   3. Fast Green: stock solution 10 mg/ml distilled H₂O
   4. Slow drying ink (less shellac and thus less poisoning for the embryo). Note: A blue dichroic filter attached to a fiber optic lamp as described in Canto-Soler and Adler¹⁴ enhances the contrast and can eliminate the need to inject ink.

Figure 1. Schematic diagram of electrodes and electrode holder. (A, B, C) Platinum wire was soldered to one side of a stainless steel tubular shaft. A hole was drilled into the other side of the tubular shaft thus that pin plugs can fit in. (A) Red and blue colored wires were connected to the pin plugs. At the opposite end the wire was fitted to banana connectors that work with the electrical sockets of the electroporator. (A, C) The platinum wire was bent in an angel of 90°. A layer of nail varnish isolated the shaft above the bend.

2. Preparations Directly Before In ovo Electroporation

1. Prepare the following material:
   1. Dilute Ink with chicken Ringer 1:6, add Antibiotic-Antimycotic solution (100x from Gibco) 1:100.
   2. Prepare vector solution: 1-2 μg/μl per specific DNA in H₂O supplemented with Fast Green (1:20).
   3. Sterilize forceps, scissors, tungsten needle and electrodes with 70% ethanol.
   4. Pull micropipettes for nucleic acid injection from borosilicate glass capillaries (length to outer diameter: 100 mm x 0.9 mm). We use a simple puller PUL-1 (WPI, Berlin) with the settings shown in Table 1.
   5. Set the parameters of the electroporator as shown in Table 2.

Parameters	Values
Heat	350
Pull	100
Velocity	50
Delay	200

Table 1. Settings for PUL-1

Parameters	Values
Frequency	50 Hz
Delay	20 - 50 msec*
Width	20 msec
Voltage	8-25 V *
Pulse	3 - 5 times
*Depending on electrode diameter and distance. Please take that into account when changing one of the parameters.

Table 2. Settings for the Pulse Stimulator

2. Prepare chick embryos for electroporation:
   1. Incubate fertilized chicken eggs on their longer side at 37 °C with 65% humidity for 39 hr to acquire embryos between Hamburger & Hamilton (HH) stages¹⁵ 9-11. The embryo settles at the topmost part of the egg, so you should mark it with a pencil line.
   2. Disinfect the eggs with 70% ethanol.
   3. Pierce the egg at its broader side, where the air cavity should be.
   4. Remove 1-2 ml of egg white. This will detach the embryo from the eggshell.
   5. Cello-tape the eggshell to avoid shell splinters falling onto the embryo. Use a pair of scissors to cut a small window into the eggshell around the pencil line.
   6. Inject a bit of ink underneath the area opaca to visualize the embryo.
   7. Make a cut into the vitelline membrane with a sharpened tungsten needle to achieve a better accessibility of the embryo for nucleic acid injection and electroporation.

3. Electroporation and Incubation

1. Add a few drops of warm Ringer's solution onto the embryos. This will lower the embryos, prevent overheating, sticking of the electrodes to the tissue and provide a medium for the current between the two electrodes.
2. Inject the vector solution into the lumen of the neural tube at midbrain level. If your DNA expression vector contains no reporter gene (e.g. EGFP), add a slightly lower concentrated reporter gene vector (1 μg/μl miR expressing vector to 0.9 μg/μl reporter gene vector) to the DNA solution. This will ensure that you recognize transfected cells later⁸. We use the so-called pCAX vector, a kind gift from C. Krull ¹³.
3. For a broad transfection of the midbrain, place the electrodes left and right of the embryo at the height of the midbrain. The distance between the electrodes should be around 3-5 mm. The other settings are 15V, 20 msec pulses and 50 msec delay for HH 10. Changing the position of the two electrodes slightly along the dorso-ventral (DV) axis of the midbrain assures a more a broad transfection of cells the DV axis transfection.
4. For ventral transfection, add some Ringer to raise the head from the yolk membrane and place the anode beneath ventral midbrain. If the head does not rise push the electrode under the membrane that separates yolk and embryo to avoid scorching of the neural tube. The cathode should be placed above the midbrain dorso-laterally opposite to the anode. Do not touch the neural tube. We transfect the left ventral half of the midbrain to avoid any difficulties with heart development. The distance between the electrodes is around 1-0.5 mm, the rest of the settings are 10V, 20 msec width and 50 msec delay.
5. Apply another drop of Saline on top of the embryos to cool it down and remove air bubbles.
6. Seal the eggs with the tape and incubate for at least 4 hr; the minimum time required for vector expression.

4. Fixation of Chicken Embryos

1. Remove the embryos from their eggs.
2. Clean embryos under a stereomicroscope and assess the extent of transfection with a fluorescent stereo microscope.
3. Fix the embryos over night in 4% PFA at 4°C. Proceed with sectioning and/or staining (in situ hybridization, immunohistochemistry) to analyse changes in the transfected area.

Results

The extent of the midbrain area transfected with miR is visible through the expression of GFP from a reporter vector injected along with the miR expressing vector (Figure 2). Using platinum electrodes with a diameter of 0.5 mm and placed parallel to the AP axis of midbrain leads normally to the transfection of a broad area along the DV- and AP- axis, including hindbrain, midbrain and sometimes diencephalon (Figures 2A and B). The size of the electrodes results in a wide electric field ap...

Discussion

This video demonstrates an effective method to transfect plasmid into the neuroepithelial cells of specific areas of the chick midbrain. Rectangular electric pulses of low voltage can introduce DNA into cells of the chick neural tube in ovo^6,16. However, the accuracy of DNA targeting is often hindered by the wide electric field, which rises through the relatively large electrodes (Φ = 0.5 mm). We tried to tackle that problem by using electrodes smaller in diameter following the guidelines of Momos...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Borosillicate glass capillaries	Hartenstein		Model: 0.9 mm
Microcapillary puller	WPI, Berlin		Model: Pul1-E
Electroporator	Intracel		Model: TSSIC
Stereomicroscope - fluorescence	LEICA		Model: MZFLIII
Stereomicroscope	Zeiss		Model: Stemi
Camera and software	Zeiss		Model: Axiocam MRc/ Axiovision Re. 4.8