Chemogenetic Silencing of Neonatal Spontaneous Activity of Projection Neurons in the Dorsal Striatum of Mice

Materials and reagents

Biological materials

1. Mice: Oprm1-2A-Cre (Oprm1-Cre [11]),

2. Virus for DREADD: pAAV-hSyn-DIO-HA-hM4D(Gi)-IRES-mCitrine (a gift from Bryan Roth, Addgene viral prep # 50455-AAV8, http://n2t.net/addgene:50455; RRID: Addgene_50455)

   
   

1. Clozapine-N-oxide dihydrochloride (HelloBio, catalog number: HB6149)

2. Sterile 0.9% NaCl (Fresenius Kabi AG, catalog number: 936808)

3. Isoflurane (1000 mg/g) (Attane vet 1000 mg/g) (Primal Critical Care, catalog number: 170579)

4. 70% EtOH (Anora Industrial, ETAX, catalog number: 1025904)

5. Hydrogen peroxide 1% (Pharmacare)

6. Glycerol 99% (Sigma-Aldrich, catalog number: G6279) or sterile PBS (Sigma-Aldrich, catalog number: P2272)

7. Green dye: Fast green FCF (Sigma-Aldrich, catalog number: F-7262)

   
   

1. CNO solution (see Recipes)

2. Green dye in glycerol solution or PBS (see Recipes)

   
   

1. CNO solution

   In a sterile 1.5 mL Eppendorf tube, measure the precise quantity of CNO powder and add sterile saline solution. Vortex well until the powder is totally dissolved. Aliquot the solution and store it at -20 °C.

   Components	Final concentration	Quantity
   CNO powder	30 mg/mL	15 mg
   NaCl	9 g/L	500 μL
   Total		~ 0.5 mL

   
   

2. Green dye in glycerol solution or PBS

   Use a sterile Eppendorf tube (0.2–1.5 mL), add 200 µL of glycerol (99%) or sterile PBS, add green dye powder for a final concentration of dye of 1%, and vortex well until it becomes green. Store the solution with PBS at 4 °C; the glycerol-based solution can be stored at room temperature.

   Components	Final concentration	Quantity
   Glycerol or PBS	99%	200 μL
   Green dye powder	1%	2 mg
   Total		200 µL

   
   

Laboratory supplies

1. NF33BV-2 33 ga. beveled NanoFil needle (World Precision Instruments, UK, catalog number: NF33BV-2)

2. NanoFil syringe 10 μL (World Precision Instruments, UK, catalog number: NANOFIL)

3. 200 μL pipette tip for making a mask (SARTORIUS, Safetyspace Tips, model: 790201)

4. T-style male luer fitting for tubing i.d. 1/8 in. to connect the mask and tubes (i.e., Sigma-Aldrich, catalog number: Z274240)

5. Scissors (World Precision Instruments, UK, catalog number: 500216)

6. Tape (Scotch Brand, Scotch® Magic™ 810, catalog number: 810-3PK-BXD)

7. Autoclavable bags (200 x 300 mm, Ratiolab, catalog number: 7001000)

8. Ice

9. Cotton buds

10. Eppendorf tube 1.5 mL (FisherBrand, catalog number: 05-408-129)

11. Eppendorf tube 0.2 mL (Nippon Genetics EUROPE GmbH, catalog number: FG-021)

12. Pipette 0.1–2 μL (Thermo Scientific™, F1-ClipTip™, catalog number: 4641310N)

13. Sterile filtered pipette tips 0.1–10 μL (SARTORIUS, Safetyspace filter tips, model: 790011F)

14. Hamilton syringe with male luer lock (25 μL), instrument syringe (Hamilton, model: 1702 TLLX, catalog number: 80222)

15. 30G syringe needles (hypodermic needle, Microlance^TM 3) (VWR, catalog number: 613-3942)

16. Blu Tack (Bostik, model: Blu Tack® Handy)

17. Wipes Kimberly-Clark^TM Kimtech Science^TM delicate task wipes (Fisher Scientific, Kimberly-Clark^TM, catalog number: 7558)

18. Gloves

19. Tunnel for mice handling (https://3rc.org/refined-mouse-handling-overview/operations-and-tunnels), e.g., cardboard tube

20. PVC tubing 1/8 in. i.d. 1/4 in. o.d. (i.e., OC-TUBING, WPI, US)

Equipment

1. Stereotaxic frame for mice (StoelTing, US, model: 51615M)

2. Temperature controller with heating pad (Supertech Instruments UK Ltd., UK, model: TMP-5b and AHP-1)

3. Micro 4 Pump controller for NanoFil syringe (World Precision Instruments, UK, model: UMP3-4)

4. Anesthesia unit (Univentor, model: Univentor 400 Anesthesia Unit with tubes, 10 mL gas-tight glass syringe; anesthesia box, model: 8329001)

5. Air pump (EHEIM GmbH & Co. KG., Germany, model: EHEIM-100)

6. Dual guide LED light illuminator (Zeiss, Germany, model: ZEISS Cold Light Source)

7. Stereo microscope on boom stand (Olympus SZ30, model: SZ3060 SZ-STB1)

Procedure

1. Viral transduction

   1. Disinfect the workstation and surgical tools with 70% EtOH. If the procedure is done in the laboratory hood, a 15–30 min UV light can also be used to disinfect the workstation and instruments before the procedure. The syringe can be sterilized by autoclaving or another method recommended by the manufacturer. Wear gloves and wash them with 70% EtOH.

   2. Use scissors to make a mask for the pup. Cut the 200 μL tip so it can be connected to the anesthesia tube. Cut the other side so the pup's nose can fit in the tube. Place the tip connected to the anesthesia tube on the heating pad and fix it on the surface using tape or blu tack.

      Note: We used a 200 μL tip and 1/8 i.d. tubes, but other materials can be used to make the mask, e.g., a 1 mL tip or a plastic Pasteur pipette tip. With these materials, it is also possible to use 1/4 i.d. tubes and fittings to place the mask.

   3. Prepare the viral vector for injection.

      1. Calculate the amount of the viral vector needed for injection, retrieve the proper amount of the aliquots from the -80 °C freezer, and thaw on ice. Always consider the extra amount needed due to possible loss of liquid when filling the syringe.

         Note: Any excess amount of the viral solution should be discarded after the procedure since thaw/freezing cycles are not recommended. Keep the virus-containing liquid on ice.

      2. Using a filtered tip, add glycerol to the viral solution (0.4–4 μL of viral aliquot). If you want to see the liquid with the virus, use glycerol or PBS with dye (see Recipes). Always use a new tip for each aliquot and discard the used tip (into an autoclavable bag or Virkon detergent solution, depending on your safety regulations).

         Note: Step A3b can be skipped. Some researchers find that adding glycerol can protect the AAV and be used for in vivo injections [12,13]. Nevertheless, the absence of glycerol should not be considered dramatic, as many effective protocols do not include this step. The dye is needed for two reasons: first, the liquid containing viral particles is visible during the injection procedure, and second, the injected liquid can be visible within the brain of the neonatal pups through the scalp [14].

      3. Mount the needle to the Nanofil syringe and attach it to the stereotaxic frame.

      4. Place the blu tack piece on the heating pad or another surface and place the tube with the virus on it. The tube should stay vertical so the syringe can be filled when attached to the frame.

      5. Using the pump, fill the NanoFil syringe with the virus-containing liquid in the amount needed to be injected for all the coordinates for one animal and 100 nL extra to compensate for liquid loss during injection or syringe itself. Use 10 nL/s pump speed for liquid withdrawal.

      6. Carefully move the syringe attached to the frame to the side, so the frame is available to place the animal.

   4. Anesthesia of the pup.

      1. Turn on a heating pad to keep at 34–35 °C. It should be warm before the animal goes to the anesthesia unit.

      2. Adjust the anesthesia unit to provide 4.7%–4.8% isoflurane anesthesia with appropriate air pressure to the unit box. Place a napkin in the box.

      3. Place the pup in the anesthesia unit box and keep it closed for at least 2 min until breathing slows down. Switch the unit to provide isoflurane to the tube with a mask.

      4. Use a small piece of wipe to make a flat pillow to support the animal's head in a horizontal position. Remove the pup and place it on the heating pad. Adjust its nose to the mask to breathe 4.7%–4.8% isoflurane. Tape the body to the heating pad with a piece of tape. When the animal is fixed on the frame, reduce isoflurane to 2%–2.5%. Check if the animal is anesthetized.

      Caution: Always follow the animal's breathing; it should not be too slow or stop. Do not push too much with the tape on the thorax and do not squeeze the pup. The tape should only be kept so that the head does not move. If the breathing is fragmented, remove the animal from the mask immediately.

   5. Viral injection.

      1. Wash the head with the cotton bud with 70% EtOH.

      2. Adjust the light so you can see lambda coordinate as an intersection of thick red vessels (see Figure 1).

         
         

         
         Figure 1. Schematic image of the setup for the viral injection procedure. A. Setup consists of an anesthetizing unit for isoflurane connected to the switcher, directing the flow to the mask or box. The air pump supplying the unit is not shown. The syringe with a needle is assembled to the injecting pump headstage. The headstage is attached to the stereotaxic frame. A heating pad is placed on the stereotaxic frame surface. The pup is positioned on the heating pad, with its nose in the anesthesia mask. A stereoscope is used to see head blood vessels and lambda. The light source is adjusted to light up the pup’s head. B. The pup is placed on the heating pad. The pup’s nose is in the cut pipette tip (mask) connected to the tube system, which provides isoflurane. The tube system is fixed on the surface of the heating pad with the blu tack. A tape is used to gently fix the head of the pup. The head is placed on the flat pillow made from the wipe. The direction of isoflurane flow is demonstrated by arrows. C. The 0 coordinate from vascular lambda is defined as the very middle of the crossing between three branches of blood vessels.

         
         

      3. Place the syringe tip to ML and AP lambda coordinates to find the 0 coordinate; then, find the coordinate needed for your purpose (for dorsal striatum: AP 2.4; ML ±1.2).

      4. Carefully and slowly move the tip down to cross the skin and skull to achieve the correct DV coordinate (for dorsal striatum, DV 2.3 and 2.7). If the tip does not go smoothly through the skull and skin, use a common 30 G syringe needle to make a small hole in the skull before pushing the injecting needle. Start with the lower coordinate.

         Note: There should not be bleeding. In case some minor bleeding occurs, use hydroxy peroxide and cotton bud to remove it. Never contact blood with the needle tip, as it will be clogged.

      5. Inject virus liquid in the needed volume (we used 150 nL). Use 5 nL/s speed. (For dorsal striatum: next, move to the upper coordinate DV 2.3 and inject the same volume again with the same speed.) Wait 5 min before moving the needle up to remove it. Remove it slowly and carefully from the head.

      6. Repeat steps A5c–A5e for the next coordinate if needed.

      7. Wash the pup’s head with the cotton bud with hydroxy peroxide and then dry it.

   6. Recovery.

      1. Remove the animal from the mask but keep it on the heating pad until it reacts to the touch and moves.

      2. Place the pup into the dam’s cage.

         
         

2. Subcutaneous CNO injections

   1. Retrieve the vial with CNO from the freezer and thaw it at room temperature.

   2. Separate pups from the dam and transfer them into the empty clean cage.

      Note: When handling active pups, it is recommended to use a plastic tunnel or a cardboard tube rather than cupped hands. See https://3rc.org/refined-mouse-handling-overview/operations-and-tunnels.

   3. Gently transfer a single pup from the cage and place it onto the weighing scale.

      Caution: Make sure to prevent the pup's escape during the weighing procedure, e.g., by placing a lid on top of the scale.

   4. Place the new needle onto the 25 μL Hamilton syringe and measure the proper volume of CNO according to the weight of the pup, with a final volume of 1 μL per gram of body weight. Control animals receive the injection of sterile saline, 1 μL per gram of body weight.

   5. Administer the injection subcutaneously into the loose skin on the neck of the pup.

      Caution: Always use different places on the skin for repeating injections.

   6. Following the injection, maintain the needle within the skin for a few seconds before gently withdrawing it to prevent any potential drug leakage from the injection site.

   7. Return the pup to the cage with the dam.

   8. Repeat the procedure for the remaining pups. Change the needle for each injection.

Data analysis

The effect of the suppression of neuronal activity during the critical developmental period was further investigated by electrophysiological recordings and immunostaining. A detailed description of performed experiments and subsequent analysis can be found in the original research article [15] under the methods section.

Validation of protocol

This protocol has been used and validated in the research article:

Kokinovic et al. [15]. Spontaneous activity of striatal projection neurons supports maturation of striatal inputs to substantia nigra dopaminergic neurons. eLife.

1. First, we validated the expression of fluorescent protein co-expressed with DREADD. A coronal slice of dorsal striatum with the expression of mCitrine is demonstrated in Figure S2B [15].

1. It is important to demonstrate the effectiveness of DREADD, which is expected to modify the firing rate of infected neurons. For example, see validation in Figure S2 C of the same publication. In this validation step, we show in vitro the effect of the 10 μM CNO on the firing rate of the striosomal SPN of a 10-day-old mouse injected by DREADD coding AAV at P0. An example trace of membrane potential recording done with whole-cell patch-clamp technique is demonstrated.

2. The outcome of the procedure for brain development was analyzed by electrophysiology and microscopy in adult mice, with results shown in Figures 6 and 7 of [15].

General notes and troubleshooting

General notes

1. Always check and follow the safety rules of your research area when handling viruses and GMO mice.

2. The procedures in this protocol require appropriate training and animal license.

3. Avoid contamination when more than one virus is used in the same setup by using different syringes for each or replaceable glass pipettes for each virus to avoid contact between the virus and the syringe. Always change filtered tips when adding glycerol or dye to each virus.

4. If more than one virus needs to be injected, they can be mixed and injected at once. The increase in the volume of injected liquid should be considered.

   
   

Troubleshooting

Problem 1: The NanoFil syringe is not injecting.

Possible cause: The tip of your needle is clogged by blood cells or another dried organic liquid.

Solution: Try to unclog the needle with a thin wire, then wash and sterilize it or simply replace it with a new one.

Problem 2: Unspecific signal in the brain tissue during validation.

Possible cause: Contamination of syringe, needle, or dye stock by another virus.

Solution: Clean and sterilize the syringe and needle and make another dye stock. Use only your own syringe, needle, and stocks.

Problem 3: No expression of the virally delivered construct after injection.

Possible cause(s): The needle did not reach the desired coordinates during injection, and all the liquid went off under the skin or into the brain ventricles; the virus prep is spoiled (i.e., it was kept at room temperature for a long time, exposed to UV light, or subjected to freezing/tawing cycles); reasons associated with construct and experiment design, such as promoter/enhancer, Cre-dependence, etc.

Solution(s): Use dye to visualize the virus-containing liquid during the injection procedure and verify that it goes inside the brain. Try another aliquot/prep for the virus injection. Check your experiment design and animal genotype.

Acknowledgments

Funding for this research was provided by the Research Council of Finland (former Academy of Finland; #330298, M.R.; #324548, S.M.) and Jane and Aatos Erkko Foundation (S.M.). The protocol outlined here was adapted from the original research paper [15].

Competing interests

The authors declare no competing interests.

Ethical considerations

All animal experiments were conducted according to the ethical guidelines (in accordance with EU directive 2010/63/EU) provided by the University of Helsinki. Breeding of the animals was done under the University of Helsinki license KEK22-013; procedures were done under the Regional State Administrative Agency of Southern Finland ESAVI/25166/2020.

References

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