Long‐Term Culture of Hippocampal Neurons

Carlos Vicario‐Abejón1

1 Centro de Investigaciones Biológicas, Censejo Superior de Investigaciones Cientificas, Madrid
Publication Name:  Current Protocols in Neuroscience
Unit Number:  Unit 3.2
DOI:  10.1002/0471142301.ns0302s26
Online Posting Date:  May, 2004
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Abstract

In culture, hippocampal cells can develop to express neuronal antigens and acquire mature neuronal morphologies, including axons, complex dendritic trees, and synapses that are electrophysiologically active. This system is suitable for studying neuronal differentiation and other events, such as synaptogenesis. It is also a valuable model for investigating synaptic plasticity and exploring the mechanisms of neuronal degeneration. This unit provides a protocol for culturing neurons prepared from embryonic (E‐18) rat or mouse hippocampus, but could also be used to grow neurons from embryonic cortex, olfactory bulb, striatum, or spinal cord. A second method is included for preparing neuronal cultures from embryos with different genotypes, such as those from transgenic mice. Also described is the preparation of polyornithine‐ and fibronectin‐coated coverslips, which are highly adhesive and promote neurite outgrowth, for use in the culture protocols.

Keywords: hippocampus; embryo; culture; rat; mouse

     
 
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Table of Contents

  • Basic Protocol 1: Culture of Hippocampal Neurons from Embryonic Day 18 Rat or Mouse
  • Alternate Protocol 1: Culture of Hippocampal Neurons from Transgenic Mouse Embryos
  • Support Protocol 1: Polyornithine/Fibronectin‐Coated Coverslips
  • Reagents and Solutions
  • Commentary
  • Literature Cited
  • Figures
     
 
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Materials

Basic Protocol 1: Culture of Hippocampal Neurons from Embryonic Day 18 Rat or Mouse

  Materials
  • Pregnant rat (e.g., Sprague‐Dawley, Taconic) or mouse, ∼18 days pregnant
  • CO 2, metophane, or ether to anesthetize animal
  • 70% ethanol
  • Dissection solution (see recipe), ice cold (keep in ice bucket)
  • Chopping solution (see recipe)
  • Trypsinization solution (see recipe)
  • Supplemented DMEM/F‐12/N2/10% FBS (see recipe)
  • Trituration solution (see recipe)
  • 0.2% to 0.4% trypan blue
  • PBS with antibiotics (see recipe)
  • Supplemented DMEM/N2/10% FBS (see appendix 2A for DMEM; see recipe for N2 supplements)
  • 1 mM cytosine β‐D‐arabinofuranoside (Ara‐C; Sigma)
  • Surgical instruments:
    • Scissors
    • Microdissecting scissors
    • Curved forceps (medium and small sizes)
    • Dumont no. 5 titanium forceps
    • Microdissecting scissors with angled blades (Castroviejo style)
  • Dissecting microscope and optic fiber lights
  • Neubauer hemacytometer
  • Inverted microscope
  • 12‐mm‐diameter polyornithine/fibronectin‐coated circular coverslips for 24‐well microtiter plate wells (see protocol 3)
  • Additional reagents and equipment for tissue culture and for cell counting using a hemacytometer and trypan blue (see appendix 3B)

Alternate Protocol 1: Culture of Hippocampal Neurons from Transgenic Mouse Embryos

  • Pregnant mouse bearing transgenic embryos, 16 to 18 days pregnant
  • DMEM/F‐12/N2 (see recipe)
  • FBS ( appendix 2A or Sigma)

Support Protocol 1: Polyornithine/Fibronectin‐Coated Coverslips

  Materials
  • Concentrated HNO 3
  • 15 µg/ml polyornithine (see recipe)
  • PBS with antibiotics (see recipe)
  • 1 µg/ml fibronectin (see recipe)
  • 12‐mm‐diameter circular coverslips for 24‐well microtiter plate wells (Bellco Glass)
  • Staining rack (cover‐glass staining outfit, Thomas Scientific)
  • Oven, 225°C
  • 24‐well microtiter plates
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Figures

Videos

Literature Cited

   Altman, J. and Bayer, S. 1990. Prolonged sojourn of developing pyramidal cells in the intermediate zone of the hippocampus and their settling in the stratum pyramidale. J. Comp. Neurol. 301:343‐364.
   Altman, J. and Bayer, S.A. 1995. Atlas of Prenatal Rat Brain Development. CRC Press, Boca Raton, Fla.
   Amaral, D.G. and Witter, M.P. 1989 The three‐dimensional organization of the hippocampal formation: A review of anatomical data. Neuroscience 31:571‐591.
   Banker, G. and Goslin, K. 1998. Culturing Nerve Cells, 2nd ed. MIT Press, Cambridge, Mass.
   Bottenstein, J.E. 1985. Growth and differentiation of neural cells in defined media. In Cell Culture in the Neurosciences (J.E. Bottenstein and G. Sato, eds.) pp. 3‐43. Plenum, New York.
   Brewer, G.J., Torricelli, J.R., Evege, E.K., and Price, P.J. 1993. Optimized survival of hippocampal neurons in B27‐supplemented neurobasal, a new serum‐free medium combination. J. Neurosci. Res. 35:567‐576.
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   Geppert, M., Goda, Y., Hammer, R.E., Li, C., Rosahl, T.W., Stevens, C.F., and Sudhof, T.C. 1994. Synaptotagmin I: A major Ca2+ sensor for transmitter release at a central synapse. Cell 79:717‐727.
   Goslin, K., Asmussen, H., and Banker, G. 1998. Rat hippocampal neurons in low‐density culture. In Culturing Nerve Cells (G. Banker and K. Goslin, eds.) pp. 339‐370. MIT Press, Cambridge, Mass.
   Harrison, R.G. 1907. Observations on the living developing nerve fiber. Anat. Rec. 1:116‐118.
   Kaufman, M.H. 1995. The Atlas of Mouse Development. Academic Press, San Diego.
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   Okabe, S., Vicario‐Abejón, C. Segal, M., and McKay, R.D.G. 1998. Survival and synaptogenesis of hippocampal neurons without NMDA receptor function in culture. Eur. J. Neurosci. 10:2192‐2198.
   Mattson, M.P., Lee, R.E., Adams, M.E., Guthrie, P.B., and Kater, S.B. 1988. Interactions between entorhinal axons and target hippocampal neurons: A role for glutamate in the development of hippocampal circuitry. Neuron 1:865‐876.
   Papa, M., Bundman, M.C., Greenberger, V., and Segal, M. 1995. Morphological analysis of dendritic spine development in primary cultures of hippocampal neurons. J. Neurosci. 15:1‐11.
   Schlessinger, A.R., Cowan, W.M., and Gottlieb, D.I. 1975. An autoradiographic study of the time of origin and the pattern of granule cell migration in the dentate gyrus of the rat. J. Comp. Neurol. 159:149‐176.
   Soriano, E., DelRío, J.A., Martínez, A., and Super, H. 1994. Organization of the embryonic and early postnatal murine hippocampus. I. Immunocytochemical characterization of neuronal populations in the subplate and marginal zone. J. Comp. Neurol. 342:571‐595.
   Super, H. and Soriano, E. 1994. The organization of the embryonic and early postnatal murine hippocampus. II. Development of entorhinal, commissural, and septal connections studied with the lipophilic tracer Dil. J. Comp. Neurol. 344:101‐120.
   Vicario, C., Tabernero, A., and Medina, J.M. 1993. Regulation of lactate metabolism by albumin in rat neurons and astrocytes from primary culture. Ped. Res. 34:709‐715.
   Vicario‐Abejón, C., Johe, K.K., Hazel, T.G., Collazo, D., and McKay, R.D.G. 1995. Functions of basic fibroblast growth factor and neurotrophins in the differentiation of hippocampal neurons. Neuron 15:105‐114.
   Vicario‐Abejón, C., Collin, C., McKay, R.D.G., and Segal, M. 1998. Neurotrophins induce formation of functional excitatory and inhibitory synapses between cultured hippocampal neurons. J. Neursci. 18:7256‐7271.
Key Reference
   Banker and Goslin, 1998. See above.
  Chapters 2, 3, and 5 discuss general principles for culturing neuronal cells, and Chapter 13 describes a protocol for culturing rat hippocampal neurons.
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