Adeno-associated Virus-mediated Transgene Expression in Genetically Defined Neurons of the Spinal Cord

Summary

Intraspinal injection of recombinase dependent recombinant adeno-associated virus (rAAV) can be used to manipulate any genetically labelled cell type in the spinal cord. Here we describe how to transduce neurons in the dorsal horn of the lumbar spinal cord. This technique enables functional interrogation of the manipulated neuron subtype.

Abstract

Selective manipulation of spinal neuronal subpopulations has mainly been achieved by two different methods: 1) Intersectional genetics, whereby double or triple transgenic mice are generated in order to achieve selective expression of a reporter or effector gene (e.g., from the Rosa26 locus) in the desired spinal population. 2) Intraspinal injection of Cre-dependent recombinant adeno-associated virus (rAAV); here Cre-dependent AAV vectors coding for the reporter or effector gene of choice are injected into the spinal cord of mice expressing Cre recombinase in the desired neuronal subpopulation. This protocol describes how to generate Cre-dependent rAAV vectors and how to transduce neurons in the dorsal horn of the lumbar spinal cord segments L3-L5 with rAAVs. As the lumbar spinal segments L3-L5 are innervated by those peripheral sensory neurons that transmit sensory information from the hindlimbs, spontaneous behavior and responses to sensory tests applied to the hindlimb ipsilateral to the injection side can be analyzed in order to interrogate the function of the manipulated neurons in sensory processing. We provide examples of how this technique can be used to analyze genetically defined subsets of spinal neurons. The main advantages of virus-mediated transgene expression in Cre transgenic mice compared to classical reporter mouse-induced transgene expression are the following: 1) Different Cre-dependent rAAVs encoding various reporter or effector proteins can be injected into a single Cre transgenic line, thus overcoming the need to create several multiple transgenic mouse lines. 2) Intraspinal injection limits manipulation of Cre-expressing cells to the injection site and to the time after injection. The main disadvantages are: 1) Reporter gene expression from rAAVs is more variable. 2) Surgery is required to transduce the spinal neurons of interest. Which of the two methods is more appropriate depends on the neuron population and research question to be addressed.

Introduction

The dorsal spinal cord is essential for information exchange between the periphery of the body and the brain. Sensory stimuli such as heat, cold, touch, or noxious stimuli are detected by specialized peripheral neurons, which convey this information to neurons of the spinal cord dorsal horn. Here, a complex network of inhibitory and excitatory interneurons modulates and eventually relays sensory information via spinal projection neurons to supraspinal sites^1,2. The computations carried out by spinal inter- and projection neurons gate sensory information, thus determining which information is suppressed or relayed at which intensity. Changes in the integration of sensory stimuli, such as an altered balance between inhibition and excitation, can cause sensory dysfunctions such as hypersensitivity or allodynia (painful sensations after normally non-painful stimulation). These changes are thought to be the underlying cause of various chronic pain states^3,4. Thus, spinal circuits are of high importance in sensory processing and consequently in the perception of an organism's environment and self. With the recent advent and combination of molecular, genetic, and surgical techniques that allow the precise manipulation of genetically identified spinal neuron subpopulations, scientists are now beginning to understand the underlying spinal circuits responsible for the processing of distinct sensory modalities.

Intraspinal injection of rAAV into wild-type or transgenic mice has greatly contributed to the manipulation, analysis, and understanding of the function of specific subsets of spinal neurons^{5,6,7,8,9,10,11}. This technique allows the delivery of marker proteins (such as GFP/ GFP fusion proteins), reporter proteins (such as GCaMP), or effector proteins (such as bacterial toxins, channelrhodopsin, or pharmacogenetic receptors) in a spatially restricted manner to spinal neurons. Local injection of Cre-dependent rAAVs into transgenic mice expressing Cre recombinase in a specific subset of spinal neurons allows the specific analysis of the respective neuronal population. We have employed this technique to label, ablate, inhibit or activate spinal glycinergic neurons demonstrating that they are an essential part of the spinal gate controlling pain and itch transmission⁷. In these experiments, intraspinal injection of Cre-dependent rAAV into GlyT2::Cre mice enabled the selective manipulation of glycinergic neurons in the lumbar spinal cord. Thereby, simultaneous manipulation of supraspinal circuits that contain glycinergic neurons critical for the survival of the animal can be avoided.

While an intraspinal injection of rAAVs limits infection to the site of injection, viral transduction can occur not only in local neurons but also in neurons that connect to the injection site via axonal projections. The latter is often used to trace CNS areas providing neuronal input to a particular nucleus in the brain. The infection of axonal projections can, however, also be a confounding factor when a defined population of neurons shall be studied at a particular site. To address these issues, we have recently conducted a comprehensive analysis of AAV serotypes and expression cassettes to identify serotypes and promoters that can be used to either minimize or maximize retrograde transduction. In the context of this specific research in spinal circuits, we analyzed the ability of different serotypes and promoters to retrogradely transduce neurons in the dorsal root ganglia (DRG), the rostral ventromedial medulla (RVM), and the somatosensory cortex¹². The technique outlined in this protocol can therefore be used either to analyze spinal neurons at the injection site or to analyze projection neurons that provide input to the injected site of the spinal cord. In the protocol described here, three injections of rAAV into the left side of the lumbar spinal cord are performed to enable transduction of neurons in the three lumbar segments (L3-L5). The L3-L5 segments receive the majority of the sensory input from the hindlimb ipsilateral to the injection site. We demonstrate that functional manipulation of genetically labeled neurons in L3-L5 is sufficient to evoke robust behavioral changes, thus providing functional evidence for the circuit function of such a genetically labeled neuron subtype.

Protocol

All animal experiments were approved by the Swiss cantonal veterinary office (Zurich) and are in accordance and compliance with all relevant regulatory and institutional guidelines.

NOTE: All materials along with respective manufacturers and/or vendors are listed in the Table of Materials.

1. Generation of Cre-dependent AAV Vectors

NOTE: A variety of Cre-dependent vectors with different promoters can be purchased (see Table of Materials) or, if the desired expression construct is not available, it can be generated by modifying existing AAV constructs. Note, the promoter and serotype can have an impact on the spread of viral transduction (see ¹²). The first part of this protocol briefly describes the generation of two different Cre-dependent AAV vectors suitable for gain and loss of function experiments, respectively.

1. Pharmacogenetic Activation (Gain of Function)
   1. Order pAAV.hSyn.flex.hM3D(Gq)-mCherry (see Table of Materials) for designer receptors exclusively activated by designer drugs (DREADD)-mediated activation.
   2. Upon receiving the bacterial stab culture, streak out bacteria on LB plates (bacteriological-grade agar dissolved in Luria-Bertani liquid medium) supplemented with the appropriate antibiotic. Incubate over night at 37 °C and pick a single colony on the next day.
      NOTE: Plasmids containing AAV vector genomes can be unstable and recombination of the viral genome, especially within the viral inverted terminal repeats (ITR), can occur during amplification in E. coli. We suggest using recA-deficient/-suppressed strains such as MDS42 or Stbl3 to avoid recombination within the plasmid containing the AAV genome.
   3. Amplify bacteria following the instructions given by the vendor of the chosen DNA-Maxi-Kit and prepare high quality plasmid DNA with a commercially available DNA-Maxi-Kit (e.g., see Table of Materials). Perform a quality control of the plasmid DNA preparation by verifying the integrity and identity of the plasmid DNA through restriction digest of an aliquot of the plasmid DNA.
      NOTE: There are recognition sites for the restriction endonuclease SmaI within the ITRs. Include a SmaI digest in the quality control to verify the integrity of the ITRs.
   4. Send the DNA to a viral vector core facility in order to produce high quality rAAV.
      NOTE: High titer, high quality viral preps are crucial for avoiding confounding phenotypes caused by contaminations in the viral prep. We therefore recommend having the rAAV of choice produced in an established vector core facility, unless the AAV production is well established in the laboratory.
2. Ablation (Loss of Function)
   NOTE: Bacterial toxins or toxin receptors can be used to mediate cell ablation or neuronal silencing. We have generated pAAV.EF1α.flex.DTA to express diphtheria toxin fragment A (DTA) in a Cre-dependent manner.
   1. To generate a Cre-dependent viral vector, choose a Cre-dependent vector with a suitable promoter (e.g., pAAV.EF1α.flex.hChR2(H134R)-eYFP). Amplify the coding sequence of choice (e.g., DTA) by polymerase chain reaction with primers that include AscI and NheI or compatible restriction endonuclease recognition sites in their overhangs (see Foster et al.⁷)
   2. Using standard molecular biology techniques, perform restriction digests of the vector DNA (pAAV.EF1α.FLEX.hChR2(H134R)-eYFP) and of the PCR-amplified insert (NheI-DTA-AscI) with the restriction endonucleases AscI and NheI. Ligate the purified fragments.
   3. Transform the ligation reaction into suitable bacteria, according to the protocol given by the supplier of the competent bacteria of choice, and plate the bacteria onto LB plates. Use recA-deficient/-suppressed strains, such as MDS42 or Stbl3, for cloning and subsequent amplification of the plasmid DNA.
   4. On the day after transformation, pick clones and inoculate them in LB medium supplemented with the appropriate antibiotic overnight at 37 °C. On the next day, extract plasmid DNA from cultured bacteria. Verify successful cloning by restriction digests and sequencing of the extracted plasmid DNA.
   5. Amplify high quality, bacterial plasmid DNA (see step 1.1.3). Send amplified DNA to a viral vector core facility for virus production.

2. Transduction of Spinal Cells

1. Preparation of Virus Solution
   Caution: Viruses are infectious reagents and should be handled according to the relevant guidelines. In most cases, rAAVs can be handled at biosafety level 1 (BSL1).
   1. On the day of injection, defrost a stock aliquot of the desired purified virus on ice and keep it on ice until directly before the injection. Avoid repeated freeze-thaw-cycles, as these will reduce the effective titer of the virus.
      NOTE: If necessary, the defrosted virus aliquot can be kept at 4 °C for up to 3 days.
   2. Dilute the virus particles in sterile 0.9% NaCl or phosphate buffered saline (PBS).
      NOTE: The appropriate titer depends on the experimental aims and should be determined experimentally. A good total viral load to start with is 3x10⁹ genome copies (3.33x10¹² GC/mL, 3x300 nL injected). Taking excess and some loss while loading the capillary into account, about 2.5 µL of virus solution will be needed for each mouse.
2. Preparation of Micropipettes for Intraspinal Injections
   1. 'Pull' thin-wall glass capillaries (outer diameter 1 mm) on a micropipette puller to create a ~5.5 mm long, shallow shank. Use a 3.0 mm heater filament and settings of program 00 with P(A) adapted as in Table 1.
      NOTE: Pulling can be done in advance. The pulled capillaries should be stored in a closed container on modeling clay to avoid dust, which could later clog the micropipette. Autoclaving of micropipettes is not necessary.
   2. Clip the shank of the pulled capillary with laminectomy forceps to a length of about 4.5 to 5 mm to create a tip opening with an inner diameter of 25-35 μm. Using a microscope with a micrometer scale, measure the inner diameter of several micropipettes to get a feeling for how large the opening should be, or measure for every micropipette.
      NOTE: A smaller tip can lead to clogging; a larger tip might cause tissue damage and difficulties to penetrate the spinal cord.
3. Preparation of Surgical Setup and Tools
   1. Ensure the equipment is clean and ready to be used. Disinfect the work area by wiping with 70% ethanol and sterilize tools by autoclaving or disinfecting them. Do not leave any disinfectant on the microliter syringe that would harm the viral vector to be used.
4. Anesthesia and Preparation of the Animal for Surgery
   NOTE: The total duration of the surgery is 60-90 min.
   1. Choose 6- to 10-week old mice to facilitate the surgical procedure.
      NOTE: If the experimental design requires it, the injection of younger or older animals is possible. Any strain and both sexes can be used in principle, but use the same background strain (e.g., C57BL/6J) for comparison of behaviors between different transgenic mouse lines. If sex differences are expected or to be investigated, analyze males and females in separate groups.
   2. Induce anesthesia using ~5% isoflurane. Place the animal in the stereotaxic frame on a heat mat and maintain anesthesia at 1-2.5% isoflurane (air flow rate 900 mL/min). Monitor the respiration rate throughout the surgery.
   3. Apply lubricant eye ointment to prevent corneal drying during the surgery.
   4. Shave the animal's back and remove hair carefully with wet tissues. Disinfect the shaved skin with iodine solution and allow the skin to dry.
   5. Give analgesic treatment (e.g., 0.1-0.2 mg/kg buprenorphine subcutaneously).
5. Exposure of the Vertebral Column at the Lumbar Spinal Cord Level
   NOTE: Due to the differential development of the spinal cord and the vertebral column, the respective levels are not aligned, but the lumbar spinal cord segment L4 is at the same level as the thoracic vertebra T13.
   1. Locate the most caudal rib pair by palpating along the vertebral column. Using a scalpel, make a 1.5-2.5 cm longitudinal cut into the skin starting from just rostral to the most caudal rib pair.
   2. Lift the skin with forceps and detach it from the underlying muscle with scissors. Throughout the surgery, keep the exposed tissues moist with sterile 0.9% NaCl.
   3. Using fine forceps and small scissors, make an incision into the next, thin membranous layer right next to the midline and cut it off from the spinous processes. It is separate from the underlying paraspinous muscle, but attached to the spinous processes.
6. Identification of the Vertebrae at the Lumbar Spinal Cord Level
   NOTE: Once the vertebral column is exposed, the intertransverse ligaments and the dorsal spinous processes should be visible. Several anatomical landmarks can aid in identifying the correct vertebra to target (Figure 1B).
   1. Pull the skin back towards the tail to expose the iliac crest. At the same level, the most caudal pair of visible intertransverse ligaments joins the L6 spinous process. Count backwards in a caudal to rostral direction to identify the vertebra of interest.
   2. Palpate along the vertebral column. The most caudal rib pair is located just rostral to the T13 vertebra and the pelvic bone at hip level is at the level of the L6 vertebra.
   3. Locate the spot where the tendon along the side of the vertebral column is whitest and most medial. The T13 vertebra is located just rostral. The lumbar spinal cord segment L4 is located within this vertebra.
7. Fixation of the Vertebral Column and Exposure of the Lumbar Spinal Cord
   1. Place the animal onto a cushion of rolled up tissues to elevate it to the spinal clamps of the stereotaxic frame.
   2. Fix the target vertebra to avoid movements of the vertebral column due to breathing. For this aim, align the clamps adjacent to the target vertebra, fix one clamp in position and hold the vertebral column with Adson forceps while fixing the second clamp.
      NOTE: The column should be perpendicular to the injection plane and firmly fixed so that it does not move upon pressure from above. If necessary, a second pair of clamps can be fixed to the vertebral column. In this case, it is useful to fix the two pairs of clamps to the two vertebrae adjacent to the target vertebra.
   3. Remove the paraspinous muscle above the vertebrae of interest. Using a scalpel, make a parallel incision just medial to the tendons that are parallel to the vertebral column, as well as perpendicular incisions rostral and caudal to the target vertebra. Be careful not to cut too deep. Tear/cut away the muscle using rongeurs. Use forceps as needed to remove tissue remaining on the vertebra or above the dura in the intervertebral space.
   4. In the intervertebral space, the dorsal blood vessel should be visible marking the midline of the spinal cord. For unilateral injections, perform a partial laminectomy by drilling a hole into the middle of the target side of the vertebra. Use a fine dentistry drilling apparatus with a 0.5 mm spherical cutter and drill especially carefully when approaching the spinal cord. Remove any remaining bone fragments with a 26G beveled needle to expose the spinal cord.
   5. Using a 26G beveled needle, perforate the dura in the drilled hole, and in the intervertebral space rostral and caudal to the target vertebra, all approximately 200 µm lateral to the dorsal blood vessel. Cerebrospinal fluid should be escaping from the holes and the spinal cord should be slightly bulging out.
8. Preparation of the Injection Syringe
   NOTE: The injection syringe should be prepared immediately before the start of the injection to reduce the risk of dust particles clogging the micropipette.
   1. Mount the glass capillary onto a microliter syringe using the removable needle compression fitting kit. Fasten the nut tightly to ensure a tight and secure fit.
   2. Fill the microliter syringe with sterile distilled water and start pressing it out with the plunger.
      NOTE: If there is too much resistance so that the water does not easily come out of the tip, the micropipette is likely blocked and should be exchanged.
   3. Mount the syringe onto a micromanipulator connected to an electronically controlled microinjector. Be careful not to touch anything with the micropipette.
   4. Using the microinjector, draw up about 1 µL of air to create a bubble between the water and the virus.
   5. Place a 2.5 µL droplet of virus solution onto a piece of paraffin film, carefully move the tip of the micropipette into the droplet using the stereotaxic frame and draw it up. Then carefully press dispense until a bit of virus solution emerges at the tip.
   6. Retract the syringe and, using a pen, mark the micropipette with a scale and note the level of the virus solution; this will facilitate the monitoring of whether the infusion is progressing as programmed.
9. Intraspinal Injections
   1. Move the tip of the micropipette above one of the holes in the dura and then down until a slight dent is noted in the dura. To target the injection to the spinal dorsal horn, move down 500 µm in 100 µm consecutive increments (speed 1 mm/s) and then 200 µm up to allow for mechanical stabilization of the tissue.
      NOTE: The final depth of the tip is 300 µm in this case, but can be adapted depending on the target area.
      1. If the tissue is resistant to penetration, the micropipette might be catching on the dura. In this case, retract and move slightly to overlie the hole, or use the needle again to perforate the dura properly before repeating the penetration attempt.
   2. Program the pump to a target injection volume of 300 nL at an injection speed of 50 nL/min and press the start button to begin the infusion.
   3. After the injection is completed, check the scale to see whether the virus level has dropped and leave the micropipette in place for an additional 3 min to allow the pressure to equilibrate before slowly retracting the syringe.
   4. Repeat step 2.9.1.-2.9.3. for the other two injection sites.
10. Suturing and Recovery
    1. Remove the spinal clamps and the cushion below the mouse.
    2. Close the wound in layers with interrupted stiches, suturing the superficial tissue layers with absorbable sutures and the skin with non-absorbable sutures. Apply iodine disinfectant on the sutured wound.
    3. Terminate the anesthesia and leave the animal on the heat mat until it recovers before returning it to its home cage.
11. Postoperative Care
    1. Monitor the health of the animal on the day of surgery, the next day, and then every 2-3 days. Ensure that the animal has a normal gait, a healthy appearance (weight, eyes, fur, and behavior), and that the wound is healing.
    2. Continue analgesic treatment (e.g., 0.1-0.2 mg/kg buprenorphine subcutaneously) as necessary, three times per day.

3. Behavioral and Morphological Analyses

1. Behavioral Analysis
   NOTE: Allow animals to accommodate to the respective setup for at least 30 min before commencing measurements to let them adapt to the new experimental environment.
   1. von Frey Test
      1. Place animals individually into individual compartments of about 10 cm x 10 cm on a metal grid floor.
      2. Stimulate the plantar surface of the hindpaw ipsilateral to the injection site with a dynamic von Frey filament. Note the force at which the animal withdraws its paw from the stimulus.
      3. Repeat five times and calculate the average withdrawal threshold from the six measurements for each animal.
   2. Pin Prick Test
      1. Place animals into individual compartments of about 10 cm x 10 cm on a metal grid floor.
      2. Stimulate the plantar surface of the hindpaw ipsilateral to the injection site with a blunted 26-G needle without penetration of skin. Score behavior as zero (no reaction) or one (reaction).
      3. Repeat 9 times with intervals of 3 min between stimulations and calculate percentage response from the 10 measurements for each animal.
   3. Injection of DREADD-ligand clozapine-N-oxide (CNO)
      1. Dissolve CNO in dimethyl sulfoxide (DMSO) to create a stock solution of 0.2 mg/µL, which can be stored at room temperature.
      2. On the day of the experiment, dilute stock solution in sterile 0.9% NaCl to 0.2 µg/µL and inject 10 µL/g body weight intraperitoneally. Inject control animals with vehicle (0.2% DMSO in 0.9% NaCl).
         NOTE: According to experience, peak effects on behaviors can be expected 1-3 h after injection, and effects should completely subside after 24 h. In the case of activation of glycinergic neurons, observed behaviors include reduced pain and itch responses. Behaviors evoked by DREADD-mediated activation of neurons will depend on the targeted subset of spinal neurons.
   4. Injection of Pruritogens to Induce Itch
      1. Dissolve pruritogens in 0.9% NaCl to solutions of 8 mg/mL (chloroquine) or 10 mg/mL (histamine). 2 h after CNO administration, inject 10 µL of pruritogen or vehicle solution subcutaneously into the plantar surface of the hindpaw ipsilateral to the spinal injection site. Alternatively, inject the pruritogen intradermally into the calf, which has been shaved one day before to reduce aversive behavior caused by the shaving itself.
   5. Videotaping to Analyze Spontaneous Nocifensive or Pruritogen-induced Itch Behaviors
      1. Place animals individually into transparent compartments (about 10 cm diameter) with a bit of bedding from their respective home-cage on the floor.
      2. Videotape the animals for 5 min to record spontaneous and for 30 min to record pruritogen-induced behaviors. Analyze the videos off-line in bins of 5 min.
   6. Pain Versus Itch Behaviors
      1. Observe and note flinching, licking, and biting behaviors.
         NOTE: Flinching and licking of the affected site are considered responses to pain, whereas biting is associated with itch.
      2. Analyze videos at normal speed, measure the time that the mouse spent licking or biting the affected site, or measure in slow motion for a more precise distinction between licking and biting reflexes. Alternatively, count the number of licking/biting/flinching bouts.
2. Morphological Analysis
   1. Perform morphological analyses from one to three weeks after injection of the virus or at the end of a behavioral experiment.
      NOTE: We have detected eGFP expression as soon as 48 h after injection, but also found that expression increases significantly within the next days and even weeks. For cells with strong reporter expression, one week of incubation (from intraspinal injection until perfusion) may be enough. For cells with weak transgene expression, viruses with weak promoters or weaker fluorophores, a longer expression may be required to ensure detectable levels.
   2. Tissue Fixation
      1. Perfuse each mouse transcardially, first with of 20 mL of ice-cold artificial cerebrospinal fluid (ACSF) solution (NaCl 125 mM, NaHCO₃ 25 mM, NaH₂PO₄ 1.25 mM, D-glucose 20 mM, KCl 2.5 mM, and CaCl2 2 mM MgSO4 1 mM), then with 100 mL of 4% ice-cold paraformaldehyde (in 0.1 M sodium phosphate buffer, pH 7.4).
         Caution: Paraformaldehyde is toxic and must be handled with care.
      2. Immediately dissect the lumbar spinal cord, and post-fix the tissue for 2 h with 4% paraformaldehyde on ice. Briefly wash the post-fixed tissue with 0.1 M sodium phosphate buffer (pH 7.4) and then incubate it in 25% sucrose solution (in 0.1 M sodium phosphate buffer, pH 7.4) overnight at 4 °C.
      3. Cut the cryoprotected tissue at 30 μm on a cryostat and mount the sections on microscope slides.
   3. Immunofluorescence Staining
      1. After brief washes in PBS, apply 300 μL of blocking solution (10% Normal donkey serum in 0.3% Triton-PBS) on the sections for 1 h at room temperature.
      2. Incubate the slides with 300 μL of the respective combinations of primary antibodies in blocking solution (see Table of Materials) over night at 4 °C. Wash the sections 3 times for 5 min each in PBS.
      3. Incubate the slides with the respective combinations of secondary antibodies in blocking solution for 1 h at room temperature. Wash the sections 3 times for 5 min each in PBS.
      4. Briefly rinse the slides in ddH₂O, then mount the coverslips using fluorescent mounting medium.
      5. Acquire fluorescent images using a confocal microscope equipped with a 20x and a 40x objective.

Results

In order to illustrate the expression levels that can be obtained by the intraspinal injection of rAAV encoding a marker protein, we first injected AAV1.CAG.eGFP into the lumbar spinal cord of wild-type mice. Three injections spaced approximately 1 mm apart produced a nearly continuous infection of lumbar spinal segments L3 to L5 (Figure 1A-C). Virus injection at a depth of 300 µm from the spinal surface leads to predominant infection of cell...

Discussion

Intraspinal injection of AAVs may become a powerful technique in a research laboratory, enabling the analysis of spinal cells with a high temporal and spatial solution. This protocol enables the transduction of the three main spinal segments innervated by sensory neurons extending their peripheral axons to the hindlimb. Transducing three segments produces robust and reproducible behavioral data. It also enables testing of a larger sensory area than possible after a single intraspinal injection. For example, the same inje...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Equipment
micropipette puller: DMZ-Universal-Electrode-Puller	Zeitz	NA
anesthesia unit: Oxymat3 oxygen concentrator	Weinmann	NA
anesthesia unit: VIP 3000 Veterinary Vaporizer	Midmark	NA
Heat mat: Mio Star Thermocare 100	Migros	717614700000
Electric shaver	Philips	BT9290
surgical microscope (OPMI pico)	Zeiss	NA
Small animal stereotaxic apparatus	Kopf	NA
Neurostar StereoDrive (optional)	Neurostar	NA
Model 51690 Cunningham mouse spinal adaptor	Harvard Apparatus	72-4811
PHD Ultra syringe pump with nanomite	Harvard Apparatus	70-3601
Hamilton 701 RN 10 μl glass microliter syringe	Hamilton	7635-01
Hamilton Removable needle (RN) compression fitting 1 mm	Hamilton	55750-01
fine dentistry drilling apparatus: Osada success 40	Osada	OS-40
spherical cutter, 0.5mm	Busch	12001005B
electronic von Frey anesthesiometer	IITC	23905
flexible von Frey hairs	IITC	#7
LSM710 Pascal confocal microscope	Zeiss	NA
0.8 NA × 20 Plan-apochromat objective	Zeiss	NA
1.3 NA × 40 EC Plan-Neofluar oil-immersion objective	Zeiss	NA
Name	Company	Catalog Number	Comments
Surgical Tools
Scalpel Handle #4, 13cm	Fine Science Tools	10004-13
Extra Fine Bonn Scissors	Fine Science Tools	14084-08
Adson forceps, 1 x 2 teeth, 12 cm	Fine Science Tools	11027-12
Friedman-Pearson rongeurs, curved, 0.7 mm cup	Fine Science Tools	16121-14
Dumont #2 laminectomy forceps	Fine Science Tools	11223-20
Olsen-Hegar needle holders, serrated, 8.5 mm clamp length	Fine Science Tools	12002-12
Fine forceps #5	Fine Science Tools	11254-20
Name	Company	Catalog Number	Comments
Consumables and Chemicals
Thin-wall glass capillary, 1mm outside diameter	World Precision Instruments	TW 100-3
Syringes (1, 5 and 20 ml)	B. Braun	(9166917V, 4606051V, 4606205V)
26G beveled needle	B. Braun	4665457
Sterile scalpel blades	B. Braun	BB523
Surgical sutures Safil Quick+ 4/0, absorbable	B. Braun	C1046220
Surgical sutures Premilene 5/0, non-absorbable	B. Braun	C0932191
Sterile PBS or saline (0.9%)		NA
Ethanol, 70% (disinfectant)		NA
Iodine solution (e.g. Braunol)	B. Braun	18380
Anaesthetics (e.g. Attane isoflurane)	Provet	2222
Aldasorber	Provet	333526
analgesics (e.g. buprenorphine: temgesic)	Indivior	GTIN: 7680419310018
Ophthalmic ointment (e.g. vita-pos)	Pharma medica	GTIN: 4031626710635
Cotton swabs (e.g. from)	IVF Hartmann	1628100
Facial tissues (e.g. from)	Uehlinger AG	2015.10018
Superfrost plus microscope slides	ThermoScientific	J1800AMNZ
Name	Company	Catalog Number	Comments
Mice
C57BL/6J mice (wildtype)	The Jackson Laboratory	RRID:IMSR_JAX:000664
Rorbtm1.1(cre)Hze/J mice (RORβCre)	The Jackson Laboratory	RRID:IMSR_JAX:023526
Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/J mice (R26Tom)	The Jackson Laboratory	RRID: IMSR_JAX:007914
Name	Company	Catalog Number	Comments
Viral vectors
AAV1.CB7.CI.eGFP.WPRE.rBG (AAV1.CAG.eGFP)	Penn Vector Core	AV-1-PV1963
AAV1.CAG.flex.eGFP.WPRE.bGH (AAV1.CAG.flex.eGFP)	Penn Vector Core	AV-1-ALL854
AAV1.CAG.flex.tdTomato.WPRE .bGH (AAV1.CAG.flex.tdTomato)	Penn Vector Core	AV-1-ALL864
AAV1.EF1a.flex.DTA.hGH (AAV1.EF1a.flex.DTA)	Penn Vector Core	Custom production
AAV1.hSyn.DIO.hM3D(Gq)-mCherry.hGH (AAV.flex.hM3D(Gi))	Penn Vector Core	Custom production
Name	Company	Catalog Number	Comments
Plasmids
pAAV.hSyn.flex.hM3D(Gq)-mCherry	Addgene	44361
pAAV.EF1α.flex.hChR2(H134R)-eYFP	Addgene	20298
Name	Company	Catalog Number	Comments
Bacteria
MDS42	ScarabGenomics
Stbl3	ThermoScientific	C737303
Name	Company	Catalog Number	Comments
Reagents
EndoFree Plasmid Maxi Kit	Quiagen	12362
NucleoBond PC 500	Machery & Nagel	740574
clozapine-N-oxide (CNO)	Enzo Life Sciences	BBL-NS105-0025
chloroquine diphosphate salt	Sigma	C6628
histamine	Sigma	H7125
Dapi	Invitrogen	D3571
Name	Company	Catalog Number	Comments
Antibodies (dilution)
Rabbit anti-GFP (1:1000)	Molecular Probes	RRID:AB_221570
Rabbit anti-NeuN (1:3000)	Abcam	RRID:AB_10711153
Goat anti-Pax2 (1 : 200)	R & D Systems	RRID:AB_10889828
Guinea pig anti-Lmx1b (1 : 10 000)	Dr Carmen Birchmeier	Muller et al. 2002
Rabbit anti-GFAP (1 : 1000)	DakoCytomation	RRID:AB_10013382
Secondary antibodies raised in donkey (1:800)	Jackson ImmunoResearch Laboratories	NA