Generation of Mouse Primary Hypothalamic Neuronal Cultures for Circadian Bioluminescence Assays

Materials and Reagents

1. 96-well plate (Corning, catalog number: 3610 )

2. BD Falcon cell strainer, 70 µm (BD Biosciences, catalog number: 352350 )

3. 100-mm culture dish

4. 35-mm dish

5. 15-ml Falcon tube

6. 10-ml serological pipette

7. Fire-polished glass pipette

8. 2-8-month-old male and female C57BL/6J mice

9. Bmal1-luciferase lentivirus (Brown et al., 2005)

10. Poly-D-lysine hydrobromide (Millipore Sigma, catalog number: P6407 )

11. Laminin (BD Biosciences, catalog number: 354232 )

12. Hank’s balanced salt solution, HBSS (PAA, catalog number: H15-008 )

13. Earle’s balanced salt solution, EBSS, with Phenol Red (Thermo Fisher Scientific, Gibco, catalog number: 24010043 )

14. Papain, suspension (Worthington Biochemical Corporation, catalog number: LS003126 )

15. Deoxyribonuclease I, DNaseI (Worthington Biochemical Corporation, catalog number: LS002058 )

16. Neurobasal medium, minus phenol red (Thermo Fisher Scientific, Gibco, catalog number: 12348017 )

17. B-27 supplement (Thermo Fisher Scientific, Gibco, catalog number: 17504044 )

18. GlutaMAX supplement (Thermo Fisher Scientific, Gibco, catalog number: 35050061 )

19. Ovomocoid (Worthington Biochemical Corporation, catalog number: LS003085 )

20. Bovine serum albumin (MilliporeSigma, catalog number: A7030 )

21. L-cysteine (MilliporeSigma, catalog number: C7352 )

22. Fetal bovine serum, FBS (Thermo Fisher Scientific, Gibco, catalog number: 10500-064 )

23. Trypan blue solution (MilliporeSigma, catalog number: T8154 )

24. Cytosine β-D-arabinofuranoside, AraC (Millipore Sigma, catalog number: C1768 )

25. Pasteur pipettes (Th. Geyer, catalog number: 7691061 )

26. 2-Mercaptoethanol (Millipore Sigma catalog number: M3148 )

27. Adhesive clear PCR seal (Biozym, catalog number: 600208 )

28. D-luciferin sodium salt (Applichem, catalog number: A1006 )

29. Polybrene, Hexadimethrine bromide (Millipore Sigma, catalog number: H9268 )

Equipment

1. Sterile laminar flow hood (Thermo Fisher Scientific, model: MSC-Advantage, catalog number: 51025411 )

2. Multimode microplate reader (Berthold Technologies, model: Tristar LB941 )

3. Fluorescence microscope (Nikon, model: Eclipse Ts2R )

4. LED unit (Nikon, model: C-LEDFL470 )

5. Fluorescence filter cube (Nikon, model: C-LED470 , Excitation: 470/40 nm, Dichroic: 500 nm, Emission: 535/55 nm)

6. 10× objective (Nikon, model: CFI Achromat ADL-10× , NA: 0.4)

7. 20× objective (Nikon, model: CFI Achromat LWD ADL-20× , NA: 0.4)

8. Hemocytometer (Laboroptik, model: Neubauer )

9. Water bath (GFL, model: 1002 )

10. Dissecting microscope (Leica, model: MZ6 )

11. Dissection scissors (Fine Science Tools, catalog number: 91402-14 )

12. Dissection forceps (Fine Science Tools, catalog number: 11000-12 )

13. No.11 scalpel (Feather, catalog number: 200210011 )

14. No.5 sharp forceps (Fine Science Tools, catalog number: 11252-20 )

15. 2 × curved forceps (Fine Science Tools, catalog number: 11274-20 )

16. Student Fine Scissors (Fine Science Tools, catalog number: 91460-11 )

Software

1. MicroWin 2000 (Labsis, https://labsis.de)

Procedure

1. Schedule matings

   1. To generate E15-16 embryos, schedule the mating day of the adult mice 15-16 d before dissection. We use 2-8-month-old adult C57BL/6J mice for mating.

   2. On the next morning, confirm successful mating by vaginal plug check as described previously (Behringer et al., 2016).

   3. Confirm pregnancy by palpitation or visually before dissection.




2. Reagent preparation

   Note: Avoid repeated freeze-thaw cycles for labile reagents.

   1. Prepare poly-D-lysine (PDL) stock solution (500 µg/ml). Divide into 5-ml aliquots and store at -20 °C.

   2. Prepare laminin stock solution (0.1 µg/µl) in PBS. Divide into 250-µl aliquots and store at -20 °C.

   3. Prepare ovo/albumin inhibition solution, containing 6 mg ovomucoid and 6 mg bovine serum albumin in 6 ml EBSS. Store at 4 °C until use.

   4. Prepare DNaseI solution, with 1,000 U DNase I in 500 µl EBSS and store at -20 °C.

   5. Prepare plating medium (Neurobasal + 2% (v/v) B27 + 2 mM Glutamax + 10% (v/v) FBS + 1× penicillin/streptomycin) and store at 4 °C until use. Equilibrate at 37 °C before adding it to the culture.

   6. Prepare feeding medium (same as plating medium, but without FBS) and store at 4 °C until use. Equilibrate at 37 °C before adding it to the culture.

   7. Prepare digestion solution (100 U Papain, 5 ml EBSS, 1.1 mM EDTA (11 µl 0.5 M EDTA), 5.5 mM cysteine (3.3 mg), 0.067 mM 2-Mercaptoethanol (2.34 µl 1 % (v/v)/14.3 M pure liquid) and 250 µl DNaseI solution), sterile filtrate with a 0.2-µm filter. Activate at 37 °C for 20-30 min before use.

   8. Prepare resuspension medium (2.7 ml EBSS, 300 µl ovo/albumin inhibition solution, 150 µl DNaseI solution).




3. PDL and laminin double coating

   1. One day before dissection coat 96-well plates with PDL and laminin.

   2. Dilute PDL stock solution with PBS to working concentration 50 µg/ml. Mix 0.5 ml PDL stock solution (500 µg/ml) with 4.5 ml PBS to prepare 5 ml diluted PDL solution (50 µg/ml).

   3. Filter with 0.2-µm filter before use.

   4. Coat the culture surface of a 96-well plate with 7.5 µg/cm² PDL. Cover the wells of a 96-well plate with 48 µl diluted PDL solution (50 µg/ml).

   5. Incubate overnight at room temperature (or at least for 2 h at 37 °C).

   6. Wash 3 times with 100 µl sterile H₂O.

   7. Allow to dry completely under a sterile cell culture hood.

   8. Thaw laminin stock solution slowly at 2-8 °C.

   9. Dilute laminin stock solution with PBS to a working concentration of 6.4 µg/ml. Mix 320 µl laminin stock solution (0.1 µg/µl) with 4.68 ml PBS to prepare 5 ml diluted laminin solution (6.4 µg/ml).

   10. Cover the PDL-coated wells with 50 µl diluted laminin solution (6.4 µg/ml). The final coating concentration will be around 1 µg/cm².

   11. Incubate for 2 h at 37 °C.

   12. Wash 3 times with sterile 100 µl PBS, add 100 µl plating medium and store at 37 °C and 5 % CO₂ in the incubator.




4. Dissection

   Note: A swiftly executed preparation procedure is crucial for cell viability. Consider practicing the procedure several times before preparing experimental samples. Before starting the dissection, ensure that required materials are in place and that all equipment is disinfected.

   1. Use embryonic day 15 to 16 (E15-16) old embryos from a pregnant mother (C57BL/6J mothers usually have 8-10 pups).

   2. Work under a laminar flow hood and always apply aseptic techniques to reduce the risk of contamination with bacteria, fungi, and mycoplasma.

   3. Sacrifice mother by cervical dislocation, open the abdominal cavity with dissection scissors and forceps. The embryos are located at the posterior part of the abdominal cavity.

   4. Carefully remove the uterus horns with two curved forceps with gentle opposite pulling motions and transfer them into a 100-mm culture dish filled with ice-cold HBSS.

   5. Extract embryos with dissection scissors and curved forceps and transfer them into a new 100-mm culture dish with ice-cold HBSS.

   6. Decapitate the embryos with dissection scissors.

   7. Hold the head in position by piercing No. 5 sharp forceps into orbital cavities and by pushing the rostral part of the brain down. Simultaneously use curved forceps to remove the outer skin and skull, by peeling them gently off from caudal to rostral. Start with the left hemisphere and then repeat that step with the right hemisphere. Carefully remove the brain with curved forceps and deposit it into a 35-mm Petri dish with ice-cold HBSS. Repeat Steps D5 to D7 for the other embryos.

      Note: Avoid applying pressure onto the tissue while extracting the brains, to maintain brain integrity. Furthermore, take care that the brains are always covered with medium, do not let them dry out.

   8. Under a dissecting microscope, isolate the hypothalami with forceps and scalpel (see Figure 1 for details). Collect them in a 35-mm dish with ice-cold HBSS and keep on ice. Use a cut 1,000-µl pipette tip or a dropper with a wide opening to transfer the dissected tissue.

      
      

      
      Figure 1. Steps for hypothalamus dissection from intact E16 brains. A. Turn the brain over so that the ventral part is facing upwards. Remove the caudal part of the brain by making a coronal cut at the posterior border of the mammillary bodies. Make a second coronal cut ~1.5 mm anterior from the first to remove the rostral part of the brain. B. Rotate the remaining brain to get a coronal orientation and make sure that the rostral part is facing upwards. Dissect the hypothalamic tissue block: make two lateral cuts ~0.5 mm each from the midline and one additional cut ventral to the anterior commissure (ac). Red dashed lines indicate the cutting positions. The dissected area is highlighted in blue. Further abbreviations: LV – lateral ventricle, Thal – thalamus, Hypo – hypothalamus, Teg – tegmentum, Med – medulla oblongata, VP – ventral pallidum, OCh – optic chiasm, 3V – 3rd ventricle, Cx – cortex, CPu – caudate putamen.

      
      

5. Dissociation and plating

   1. Transfer dissected hypothalami into a 15-ml Falcon tube, remove remaining HBSS and add 5 ml digestion solution.

   2. Digest the tissue pieces for 30-60 min at 37 °C while stirring gently every 4-5 min.

      Note: A longer digestion period may increase cell yield, but it will also decrease viability. The incubation time must be determined empirically. Start with 30 min, determine yield and viability as described in Step E13. Increase incubation time if necessary.

   3. Triturate 13 times with a 10-ml serological pipette.

   4. Carefully and slowly triturate 13 times with a fire-polished glass pipette. Avoid creating bubbles during trituration.

   5. Wait 2 min for remaining undissociated tissue to settle and transfer supernatant into a new 15- ml Falcon tube.

   6. Centrifuge at 300 × g for 5 min.

   7. Remove the clear supernatant and resuspend the cell pellet with 3 ml resuspension medium.

   8. Gently triturate 7 times with a fire-polished glass pipette.

   9. Remove remaining tissue clumps by using a 70 µm cell strainer.

   10. Carefully and slowly transfer the cell suspension to 5 ml ovo/albumin inhibition solution in a 15-ml Falcon tube and centrifuge at 70 × g for 5 min to prepare a discontinuous density gradient.

   11. Remove supernatant.

   12. Add 2-3 ml plating medium and resuspend 7 times with a fire-polished glass pipette.

   13. Quantify the number of viable cells by trypan blue exclusion assay (e.g., with a Neubauer chamber).

   14. Seed 3.25 × 10⁵ viable cells/cm² in plating medium into a 96-well plate double coated with PDL and laminin.




6. Feeding and lentiviral transduction with Bmal1-luciferase reporter

   1. On the next day, transduce the cells with Bmal1-luciferase lentivirus (Brown et al., 2005). Details for lentiviral particle production are described in Tsang et al. (2020).

      Note: It is recommended to use a GFP-expressing control virus to determine transduction efficiency.

   2. Thaw lentiviral aliquots at room temperature immediately before use. Avoid keeping them for prolonged times at ambient temperature and avoid unnecessary freeze-thaw cycles.

   3. Prepare several lentiviral dilutions (e.g., 0, 1:5, 1:50. 1:250) in feeding medium containing 16 µg/ml polybrene.

      Note: It is recommended testing at least three different concentrations to determine the optimal transduction conditions. We transduced the cells with ~ 1 × 10⁸ infection units (IFUs) per 1 ml in the presence of 8 µg/ml polybrene.

   4. Replace half of the volume of the plating medium by half of the volume of lentiviral particle-containing feeding medium.

   5. 24 h later, refresh half of the volume of the old medium with fresh feeding medium containing 5 µM AraC.

   6. Feed the cells every 3 d with feeding medium, as above, but without AraC.

      Note: It is recommended to perform quality control experiments to ensure that the prepared culture is free from microbial contamination (e.g., bacteria, fungi, or mycoplasma). Mycoplasma contamination can be tested by using PCR-based detection kits (LookOut Mycoplasma PCR Detection Kit, MilliporeSigma). Although cell identification and integrity tests are commonly performed in cell culture, they are not necessary for these primary cultures, since isolated cells are directly used for the experiment and not maintained for longtime.




7. Synchronization and bioluminescence measurements

   1. On day 9 in vitro (DIV9), synchronize the cells for 2 h with 100 nM dexamethasone. Therefore, pipette 25 µl pre-warmed feeding medium containing 900 nM dexamethasone into the wells containing 200 µl medium and incubate for 2 h at 37 °C and 5% CO₂.

   2. During incubation prepare the feeding medium containing 0.5 mM D-luciferin and place it into a water bath at 37 °C.

      Note: D-luciferin is light sensitive. Protect from light.

   3. After incubation aspirate medium and change to pre-warmed feeding medium with 0.5 mM D-luciferin.

   4. Seal the plate with transparent adhesive foil, place it into the microplate reader and start the measurement.

   5. Perform the luminescence measurement without filter at 34 °C with an integration time of 1 min per well.

   6. Normalize all bioluminescence traces by subtracting the 24-h running average and analyze circadian parameters as described previously (Landgraf et al., 2015).

      Note: Synaptic formation starts to be evident at DIV7 (Figure 2). Neurons are considered to be mature at DIV14 (Biffi et al., 2013; Kos et al., 2016). We use DIV9 neurons for standard circadian luciferase experiments. Bmal1-luciferase reporter rhythms are stable for a week without further medium refreshing during the recording.

Figure 2. Synaptic connectivity increases with days in vitro. Representative bright-field (left) and fluorescence (right) images of primary hypothalamic neurons transduced with a GFP-expressing lentivirus. 10× and 20× magnification.

Data analysis

The Mikrowin2000 software allows real-time monitoring of bioluminescence signals. Bmal1-luciferase rhythms are plotted and displayed. During the measurement, wells of interest can be selected and examined. Mikrowin2000 continuously saves the experiment as a *.dat file, which can be opened by the software once the measurement procedure has been completed. To analyze the data, export the raw data to Excel. Calculate the 24-h running average and subtract that from baseline readings for normalization (Figure 3). We use GraphPad Prism for plotting, sine wave fitting, rhythm parameter determination and statistical analyses. Statistical assessment of rhythmicity is done with JTK_cycle or CircaCompare (Hughes et al., 2010; Parsons et al., 2020).

Figure 3. Bioluminescence measurements of synchronized primary hypothalamic neurons expressing Bmal1-luciferase. Bioluminescence traces are normalized by subtracting their 24-h running average. Circadian parameters, such as amplitude, period (wavelength), and dampening rate (K) are determined by fitting a damped sine wave function (Y = Amplitude*exp(-K*X)*sin((2*pi*X/Wavelength) + Phase shift). A. Representative raw data (black) and the calculated 24-h running average (red). B. Representative normalized data (black) and damped sine wave fit (blue). C. Quantification of period, amplitude and dampening rate. Data are presented as mean ± SEM (n = 6).

Acknowledgments

This study was supported by funds of the German Research Foundation (DFG; OS353-7/1, OS353-10/1 and GRK-1957). The protocol was used for Tsang et al. (2020).

Competing interests

The authors report no conflict of interest.

Ethics

Animal experiments reported in this protocol have been approved by the ethics commission of the Ministry of Energy Change, Agriculture, Environment and Digitalization (MELUR) of the State of Schleswig-Holstein (Az 4_2019-10-01_Oster; 2019-2021).

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