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Neurosphere contains neural stem cells that are capable of self-renewal and multilineage differentiation including neurons, astrocytes, and oligodendrocytes (Gage, 2000). Cell culture model using differentiated neurosphere cultures are suggested to be a valuable tool for studying the pathogenesis of prion disease at the cellular level (Iwamaru et al., 2013). This protocol describes the procedure for a culture of whole brain-derived neurospheres from newborn mouse brains. Neurosphere formation steadily occurs within a week from the cultures of neonatal whole brains and these cells have stem cell properties.

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Isolation and Culture of Neurospheres for the Study of Pathogenesis of Prion Disease

Neuroscience > Development > Neuron
Authors: Yoshifumi Iwamaru
Yoshifumi IwamaruAffiliation: Influenza and Prion Disease Research Center, National Institute of Animal Health (NIAH), Tsukuba, Japan
Bio-protocol author page: a1216
Takato Takenouchi
Takato TakenouchiAffiliation: Division of Animal Sciences, National Institute of Agrobiological Sciences, Tsukuba, Japan
Bio-protocol author page: a1217
 and Hiroshi Kitani
Hiroshi KitaniAffiliation: Division of Animal Sciences, National Institute of Agrobiological Sciences, Tsukuba, Japan
For correspondence: kitani@affrc.go.jp
Bio-protocol author page: a1218
Vol 4, Iss 6, 3/20/2014, 5623 views, 0 Q&A, How to cite
DOI: https://doi.org/10.21769/BioProtoc.1081

[Abstract] Neurosphere contains neural stem cells that are capable of self-renewal and multilineage differentiation including neurons, astrocytes, and oligodendrocytes (Gage, 2000). Cell culture model using differentiated neurosphere cultures are suggested to be a valuable tool for studying the pathogenesis of prion disease at the cellular level (Iwamaru et al., 2013). This protocol describes the procedure for a culture of whole brain-derived neurospheres from newborn mouse brains. Neurosphere formation steadily occurs within a week from the cultures of neonatal whole brains and these cells have stem cell properties.

Keywords: Neural stem cell, Isolation and culture, Neurosphere, Neonatal mouse brain, Prion protein

Materials and Reagents

  1. Newborn mice (age at one day after birth)
    Present culture method can be applied to any mouse strains, regardless of sex. We used prion protein overexpressing transgenic mouse and prion protein-deficient mouse for our present study (Iwamaru et al., 2013).
  2. Dulbecco's phosphate buffered saline without Ca and Mg (D-PBS) (Nacalai Tesque, catalog number: 14249-95)
  3. Di‐sodium dihydrogen ethylenediamine tetraacetate dihydrate (EDTA) (Nacalai Tesque, catalog number: 151-11)
  4. Hank's balanced salt solution (HBSS) (Sigma-Aldrich, catalog number: H8264)
  5. Dulbecco's modified Eagle's medium/nutrient mixture F-12 Ham (DMEM/F12 Ham) (Sigma-Aldrich, catalog number: D8437)
  6. N-2 supplement (Life Technologies, catalog number: 17502-048)
  7. Penicillin-Streptomycin (Sigma-Aldrich, catalog number: P0781)
  8. Fetal bovine serum (FBS) (Hyclone, catalog number: SH30070.03)
  9. Accutase (Innovative Cell Technologies, catalog number: AT104)
  10. Trypsin (Sigma-Aldrich, catalog number: T8003) (see Recipes)
  11. Deoxyribonuclease I (DNase I) (Worthington Biochemical Corporation, catalog number: LS002139) (see Recipes)
  12. Epidermal growth factor human (EGF) (Sigma-Aldrich, catalog number: E9644) (see Recipes)
  13. Fibroblast growth factor-basic human (bFGF) (Sigma-Aldrich, catalog number: F0291) (see Recipes)
  14. Bovine serum albumin (BSA) (Sigma-Aldrich, catalog number: A9576) (see Recipes)
  15. Neurosphere basal medium (see Recipes)

Equipment

  1. Falcon 15 ml conical centrifuge tube (Corning, catalog number: 352096)
  2. Falcon 100 mm cell culture dish (Corning, catalog number: 353003)
  3. Nunc 60 mm dish with HydroCell surface (Thermo Fisher Scientific, catalog number: 174912)
  4. Disposable micro homogenizer (TaKaRa Bio, TaKaRa BioMasher Standard, catalog number: 9791A)
  5. Aerosol resistant tip (ART 1000 REACH tips) (Thermo Fisher Scientific, model: 2079)
  6. Membrane filter (EMD Millipore, Millex-GV 0.22 μm, 33 mm)
  7. Dissecting microscope (Olympus, model: SZH10)
  8. Centrifuge (KUBOTA, model: 5220)
  9. CO2 incubator (set at 37 °C and 5% CO2-95% air)
  10. Reciprocal shaker (TAITEC, model: NR-1)
  11. Laminar flow hood (W800 x H1050 x D500 mm) (Panasonic Corporation, SANYO, model: MCV-710ATS)
  12. Scissors (NAPOX B-5H, 154 mm; NAPOX B-1112H, 110 mm), fine forceps (NAPOX A-5, 110 mm; NAPOX MA-45, 110 mm), spatula (Laboran 9-891-03, 180 mm)
  13. Ice bucket

Procedure

  1. Dissect the brain from newborn mice under Laminar flow hood (Figure 1). Spray 70% ethanol upon newborn mice and cut the head (Figure 2A). Make small incisions (Figure 2B, arrows) and remove the skin. Then, carefully remove the skull with forceps and expose the brain (Figure 2C).


    Figure 1. Dissecting equipments arranged in a Laminar flow hood


    Figure 2. Dissection procedures to obtain neonatal mouse brain

  2. Scoop the brain by a small spatula and place them in ice cold HBSS (10 ml in 100 mm dish, Figure 3A). By using fine forceps, remove meninges under dissecting microscope (Figure 3B-C).


    Figure 3. Removal of meninges (B: arrow) from neonatal mouse brain under dissecting microscope. After removal of meninges, the brain becomes whitish color (C).

  3. Place cortices in sterilized disposable micro homogenizer and centrifuge at 5000 x g for 30 sec at 4 °C.
  4. Pipet the minced tissue with 2 ml of D-PBS containing 1 mM EDTA, 100 μg/ml trypsin, and 400 μg/ml DNase I until evenly homogenized and place them in a 15 ml Conical Centrifuge Tube.
  5. Incubate for 15 min at 37 °C in an incubator with constant agitation using a reciprocal shaker at 50 rpm. Add 1 ml of FBS, then gently pipet up and down to help the dissociation by using aerosol resistant tip to avoid contamination. Stand tubes for 2 min at 25 °C and collect supernatant by pipetting. Avoid to suck any visible tissue fragments.
  6. Centrifuge cell suspensions at 200 × g for 5 min at 25 °C and resuspend the pellet in Neurosphere basal medium (10 ml) by pipetting.
  7. Centrifuge the cell suspension at 200 x g for 5 min at 25 °C. Discard the supernatant, resuspend in 5 ml of Neurosphere basal medium at 25 °C and transfer it into Nunc 60 mm dishes with HydroCell Surface. Culture the cells at 37 °C in humidified CO2 incubator (5% CO2-95% air).
  8. Refill 0.5 ml of Neurosphere basal medium everyday.
  9. After 5-7 days, neurospheres with variable sizes (50-100 μm in diameter) are formed in the culture (Figure 4). Centrifuge neurosphere suspensions at 200 × g for 5 min at 25 °C, discard the supernatant, and resuspend in 2 ml of Accutase at 37 °C for 10 min.


    Figure 4. Neurosphere formation in Neurosphere basal medium after 5 days of culture. Scale bar = 100 μm

  10. Gently pipet up and down (about ten times) using aerosol resistant tip to dissociate into single cells. Check the cells under microscope for successful dissociation. Add 12 ml of HBSS and centrifuge at 200 x g for 5 min at 25 °C. Resuspend the pellet in 10 ml of Neurosphere basal medium at 25 °C and subculture into new Nunc 60mm dishes with HydroCell Surface at 1:4 split ratio (i.e. 25% of the harvested cells are seeded into the new dish with same size). Refill 0.5 ml of Neurosphere basal medium everyday. The neurospheres are subcultured at 4-6 day intervals.

Recipes

  1. Deoxyribonuclease I (DNase I)
    Dissolved at 4 mg /ml in D-PBS
    Sterile filtered (0.22 μm)
    Aliquoted (4 ml) and stored at -20 °C
    Use within 6 months
  2. Epidermal growth factor human (EGF)
    Dissolved at 50 μg /ml in sterile DMEM/F12 Ham containing 1% BSA
    Aliquoted (100 μl) and stored at -20 °C
    Use within 6 months
  3. Fibroblast growth factor-basic human (bFGF)
    Dissolved at 50 μg /ml in sterile DMEM/F12 Ham containing 1% BSA
    Aliquoted (50 μl) and stored at -20 °C
    Use within 6 months
  4. Bovine serum albumin (BSA)
    Dissolved at 300 mg /ml in D-PBS
    Sterile filtered (0.22 μm)
    Stored at 4 °C
    Use within 6 months
  5. Neurosphere basal medium
    Reagents
    Volume
    Final conc.
    DMEM/F12 Ham
    487.33 ml

    EGF
    500 μl
    50 ng/ml
    bFGF
    500 μl
    50 ng/ml
    BSA
    1.67 ml ml
    0.1%
    N2 supplement
    5 ml
    1%
    Penicillin-streptomycin
    5 ml
    100 IU/ml and 100 μg/ml, respectively
  6. Trypsin
    Dissolved at 1 mg /ml in D-PBS containing 10 mM EDTA
    Sterile filtered (0.22 μm)
    Aliquoted (4 ml) and stored at -20 °C
    Use within 6 months
    For the dissociation of minced brain tissue, mix the reagents as follows:
    Reagents
    Volume
    Final conc.
    Trypsin
    1 ml
    100 μg/ml
    DNase I
    1 ml
    400 μg/ml
    D-PBS
    8 ml


Acknowledgments

This protocol was adapted from our previously published paper: Iwamaru et al. (2013). This work was supported by a Grant-in-Aid from the BSE and Other Prion Disease Control Project of the Ministry of Agriculture, Forestry, and Fisheries of Japan and by a Grant-in-Aid for Young Scientists (category B) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

References

  1. Gage, F. H. (2000). Mammalian neural stem cells. Science 287(5457): 1433-1438.
  2. Iwamaru, Y., Takenouchi, T., Imamura, M., Shimizu, Y., Miyazawa, K., Mohri, S., Yokoyama, T. and Kitani, H. (2013). Prion replication elicits cytopathic changes in differentiated neurosphere cultures. J Virol 87(15): 8745-8755.


How to cite: Iwamaru, Y., Takenouchi, T. and Kitani, H. (2014). Isolation and Culture of Neurospheres for the Study of Pathogenesis of Prion Disease. Bio-protocol 4(6): e1081. DOI: 10.21769/BioProtoc.1081; Full Text



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