Skip to main content

Preparation, Maintenance, and Use of Serum-Free Aggregating Brain Cell Cultures

  • Protocol
  • First Online:
In Vitro Neurotoxicology

Part of the book series: Methods in Molecular Biology ((MIMB,volume 758))

Abstract

Serum-free aggregating brain cell cultures are free-floating three-dimensional primary cell cultures able to reconstitute spontaneously a histotypic brain architecture to reproduce critical steps of brain development and to reach a high level of structural and functional maturity. This culture system offers, therefore, a unique model for neurotoxicity testing both during the development and at advanced cellular differentiation, and the high number of aggregates available combined with the excellent reproducibility of the cultures facilitates routine test procedures. This chapter presents a detailed description of the preparation, maintenance, and use of these cultures for neurotoxicity studies and a comparison of the developmental characteristics between cultures derived from the telencephalon and cultures derived from the whole brain. For culture preparation, mechanically dissociated embryonic brain tissue is used. The initial cell suspension, composed of neural stem cells, neural progenitor cells, immature postmitotic neurons, glioblasts, and microglial cells, is kept in a serum-free, chemically defined medium under continuous gyratory agitation. Spherical aggregates form spontaneously and are maintained in suspension culture for several weeks. Within the aggregates, the cells rearrange and mature, reproducing critical morphogenic events, such as migration, proliferation, differentiation, synaptogenesis, and myelination. For experimentation, replicate cultures are prepared by the randomization of aggregates from several original flasks. The high yield and reproducibility of the cultures enable multiparametric endpoint analyses, including “omics” approaches.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 159.00
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 109.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Honegger, P., Lenoir, D., and Favrod, P. (1979) Growth and differentiation of aggregating fetal brain cells in a serum-free defined medium. Nature 282, 305–308.

    Article  PubMed  CAS  Google Scholar 

  2. Herculano-Houzel, S. and Lent, R. (2005) Isotropic fractionator: a simple, rapid method for the quantification of total cell and neuron numbers in the brain. J. Neurosci. 25, 2518–2521.

    Article  PubMed  CAS  Google Scholar 

  3. Pakkenberg, B., Pelvig, D., Marner, L., Bundgaard, M.J., Gundersen, H.J., Nyengaard, J.R., and Regeur, L. (2003) Aging and the human neocortex. Exp. Gerontol. 38, 95–99.

    Article  PubMed  Google Scholar 

  4. Honegger, P. and Monnet-Tschudi, F. (2001) Aggregating neural cell cultures. In S. Fedoroff and A. Richardson (eds.) Protocols for Neural Cell Culture, 3rd ed., Humana Press, Totowa, N.J. pp. 199–218.

    Chapter  Google Scholar 

  5. Honegger, P. and Schilter, B. (1992) Serum-free aggregate cultures of fetal rat brain and liver cells: Methodology and some practical application in neurotoxicology. In G. Zbinden (ed.) In Vitro Techniques in Neurobiology, Neuro-pharmacology and Neurotoxicology, MTC Verlag, Zollikon, Switzerland, pp. 51–79.

    Google Scholar 

  6. Honegger, P. and Schilter, B. (1995) The use of serum-free aggregating brain cell cultures in neurotoxicology. In L.W. Chang (ed.) Neurotoxicology: Approaches & Methods, Academic Press, New York, USA, pp. 507–516.

    Chapter  Google Scholar 

  7. Zurich, M.-G., Monnet-Tschudi, F., Costa, L.G., Schilter, B. and Honegger, P. (2004) Aggregating brain cell cultures for neurotoxicological studies. In E. Tiffani-Castiglioni (ed.) Methods in Pharmacology and Toxicology: In vitro Neurotoxicology, Principles and Challenges, Totowa, New Jersey, USA, pp. 243–266.

    Chapter  Google Scholar 

  8. Monnet-Tschudi, F., Zurich, M.-G., Boschat, C., Corbaz, A., and Honegger, P. (2006) Involvement of environmental mercury and lead in the etiology of neurodegeneraqtive diseases. Rev. Environmental Health 21,105–117.

    CAS  Google Scholar 

  9. Monnet-Tschudi, F., Zurich, M.-G., and Honegger, P. (2007) Neurotoxicant-induced inflammatory response in three-dimensional brain cell cultures. Human Exp. Toxicol. 26, 339–346.

    Article  CAS  Google Scholar 

  10. Zurich, M.-G., Lengacher, S., Braissant, O., Monnet-Tschudi, F., Pellerin, L., and Honegger, P. (2005) Unusual astrocyte reactivity caused by the food mycotoxin ochratoxin A in aggregating rat brain cell cultures. Neuroscience 134, 771–782.

    Article  PubMed  CAS  Google Scholar 

  11. Pardo, B. and Honegger, P. (1999) Selective neurodegeneration induced in rotation-mediated aggregate cell cultures by a transient switch to stationary culture conditions: a potential model to study ischemia-related pathogenic mechanisms. Brain Res. 818, 84–95.

    Article  PubMed  CAS  Google Scholar 

  12. Monnet-Tschudi, F., Zurich, M.-G., Schilter, B., Costa, L.G., and Honegger, P. (2000) Maturation-dependent effects of chlorpyrifos and parathion and their oxygen analogs on acetylcholinesterase and neuronal and glial markers in aggregating brain cell cultures. Toxicol. Appl. Pharmacol. 165, 175–183.

    Article  PubMed  CAS  Google Scholar 

  13. Honegger, P., and Tenot-Sparti, M. (1992) Developmental effect of basic fibroblast growth factor and platelet-derived growth factor on glial cells in a three-dimensional cell culture system. J. Neuroimmunol. 40, 295–304.

    Article  PubMed  CAS  Google Scholar 

  14. Honegger, P., and Pardo, B. (1999) Separate neuronal and glial Na+,K+-ATPase isoforms regulate glucose utilization in response to membrane depolarization and elevated potassium. J. Cerebral Bloods Flow and Metabol. 19, 1051–1059.

    Article  CAS  Google Scholar 

  15. Besson Duvanel, C., Monnet-Tschudi, F., Braissant, O., Matthieu, J.-M., and Honegger, P. (2004) Tumor necrosis factor-α and αB-Crystallin up-regulation during antibody-mediated demyelination in vitro: a putative protective mechanism in oligodendrocytes. J. Neurosci. Res. 78, 711–722.

    Article  Google Scholar 

  16. van Vliet, E., Morath, S., Eskes, C., Linge, J., Rappsilber, J., Honegger, P., Hartung,T., Coecke S. (2008) A novel in vitro metabolomics approach for neurotoxicity testing, proof of principle for methyl mercury chloride and caffeine. Neurotoxicology. 29, 1–12.

    Article  PubMed  Google Scholar 

  17. Dunnett, S.B. and Björklund, A. (1992) Staging and dissection of rat embryos. In: Neural Transplantation. A Practical Approach. (S.B. Dunnett and A. Björklund, eds.) The Practical Approach Series, D. Rickwood and B.D. Hames, series eds., IRL Press, Oxford, pp. 1–19.

    Google Scholar 

  18. Cole, R. and de Vellis, J. (2001) Preparation of astrocytes, oligodendrocytes, and microglia cultures from primary rat cerebral cultures. In S. Fedoroff and A. Richardson (eds.) Protocols for Neural Cell Culture, 3rd ed., Humana Press, Totowa, N.J., pp. 117–127.

    Chapter  Google Scholar 

  19. Barroso-Chinea, P., Castle, M., Aymerich, M.S., Perez-Manso, M., Erro, E., Tunon, T. and Lanciego, J.L. (2007) Expression of the mRNAs encoding for the vesicular glutamate transporters 1 and 2 in the rat thalamus. J. Comp. Neurol. 501, 703–715.

    Article  PubMed  CAS  Google Scholar 

  20. Forsby, A., Bal-Price, A.K., Camins, A., Coecke, S., Fabre, N., Gustafsson, H., Honegger, H., Kinsner-Ovaskainen, A., Pallas, M., Rimbau, V., Rodrìguez-Farré, E., Sunol, C., Vericat, J.A., and Zurich, M.-G. (2009) Neuronal in vitro models for the estimation of acute systemic toxicity. Toxicol In Vitro 23, 1564–1569.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors are grateful to Ms Denise Tavel and Ms Brigitte Delacuisine for excellent technical assistance. This work was supported by the EU-FP6 grant (FP6-LIFESCIHEALTH-2004-512051) and by the 3R Research Foundation Switzerland.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Marie-Gabrielle Zurich .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2011 Springer Science+Business Media, LLC

About this protocol

Cite this protocol

Honegger, P., Defaux, A., Monnet-Tschudi, F., Zurich, MG. (2011). Preparation, Maintenance, and Use of Serum-Free Aggregating Brain Cell Cultures. In: Costa, L., Giordano, G., Guizzetti, M. (eds) In Vitro Neurotoxicology. Methods in Molecular Biology, vol 758. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-170-3_6

Download citation

  • DOI: https://doi.org/10.1007/978-1-61779-170-3_6

  • Published:

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61779-169-7

  • Online ISBN: 978-1-61779-170-3

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics