Skip to main content
Log in

Optimized and efficient preparation of astrocyte cultures from rat spinal cord

  • Original paper
  • Published:
Cytotechnology Aims and scope Submit manuscript

Abstract

Astrocytes constitute a major class of glial cells in the CNS, and play crucial roles in physiological functioning, performance and maintenance of the CNS, as well as promotion of neuronal migration and maturation. Astrocytes have also been directly and indirectly implicated in the pathophysiology of various trauma occurrences, development of neurodegenerative diseases and nerve regeneration. To further understand mechanisms by which astrocytes elicit these effects, the first critical step in the study of astrocytes is the preparation of purified astrocytes cultures. Here we describe a simple and convenient procedure for producing rat primary astrocyte cultures of high purity, viability and proliferation. For astrocyte culture, we have optimized the isolation procedures and cultivation conditions including coating substrates, enzyme digestion, seeding density and composition of the culture medium. Using immunofluorescent antibodies against GFAP and OX-42 in combination of Hoechst 33342 fluorescent staining, we found that the purity of the astrocyte cultures was >99%. Astrocytes had high viability as measured by 3-(4, 5-dimethyl-2-yl)-2, 5-diphenyl-2H-tetrazolium bromide (MTT) assay. In addition, flow cytometric analysis was used to measure and observe variations in the cell cycle after 1–2 passages and proliferation of astrocytes was detected with a high percentage of cells stand in S+G2/M phase. Therefore, the method described here is ideal for experiments, which require highly pure astrocyte cultures.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Allan S (2005) The neurovascular unit and the key role of astrocytes in the regulation of cerebral blood flow. Cerebrovasc Dis 21:137–138

    Article  Google Scholar 

  • Aronica E, Catania MV, Geurts J, Yankaya J, Troost D (2001) Immunohistochemical localization of group I and II metabotropic glutamate receptors in control and amyotrophic lateral sclerosis human spinal cord: upregulation in reactive astrocytes. Neurosci 105:509–520

    Article  CAS  Google Scholar 

  • Aronica E, Gorter JA, Ijlst-Keizers H, Rozemuller AJ, Yankaya B, Leonstra Troost D (2003) Expression and functional role of mGluR3 and mGluR5 in human astrocytes and glioma cells: opposite regulation of glutamate transporter proteins. Eur J Neurosci 17:1–13

    Article  Google Scholar 

  • Avola R, Condorelli DF, Surrentino S, Turpeenoja L, Costa A, Giuffrida Stella AM (1988) Effect of epidermal growth factor and insulin on DNA, RNA, and cytoskeletal protein labeing in parmary rat astrocyglial cell cultures. J Neurosci Res 19:230–238

    Article  CAS  Google Scholar 

  • Avola R, Reale S, Costa A, Insirello L, Spina-Purrello V, Giuffrida-Stella AM (1993) Effects of bFGF and IGF-I on polyadenylated RNA and non-histone chromosomal protein labeling in cultured astrocytes. J Neurochem 61:200–210

    Article  Google Scholar 

  • Ciccarelli R, Sureda FX, Casabona G, Di Iorio P, Caruso A, Spinella F (1997) Opposite influence of the metabotropic glutamate receptor subtypes mGlu3 and -5 on astrocyte proliferation in culture. Glia 21:390–398

    Article  CAS  Google Scholar 

  • Estin C, Vernadakis A (1986) Primary glial cells and brain fibroblasts: interactions in culture. Brain Res Bull 16:723–731

    Article  CAS  Google Scholar 

  • Frangakis MV, Kimelberg HK (1984) Dissociation of neonatal rat brain by dispase for preparation of primary astrocyte cultures. Neurochem Res 9:1689–1698

    Article  CAS  Google Scholar 

  • Gallo F, Morale MC, Farinella Z, Avola R, Marchetti B (1996) Growth factors released from astroglial cells in primary culture participate in the cross talk between luteinizing hormone-releasing hormone (LHRH) neurons and astrocytes. Effects on LHRH neuronal proliferation and secretion. Ann N Y Acad Sci 784:513–516

    Article  CAS  Google Scholar 

  • Goldman JE (1996) Developmental origins of astrocytes. In: Jessen KR, Richardson WD, (eds), Glial cell development Oxford: BIOS Scientific pp 31

    Google Scholar 

  • Haberg A, Qu H, Sonnewald U (2006) Glutamate and GABA metabolism in transient and permanent middle cerebral artery occlusion in rat: importance of astrocytes for neuronal survival. Neurochem Int 48:531–540

    CAS  Google Scholar 

  • Hansoson E, Ronnback L (2003) Glial neuronal signaling in the central nervous system. FASEB J 17:341–348

    Article  Google Scholar 

  • Kim JA, Tran ND, Wang SJ, Fisher MJ (2003) Astrocyte regulation of human brain capillary endothelial fibrinolysis. Thromb Res 112:159–165

    Article  CAS  Google Scholar 

  • Lang B, Liu HL, Liu R, Feng GD, Jiao XY, Ju G (2004) Astrocytes in injured adult rat spinal cord may acquire the potential of neural stem cells. Neurosci 128:775–783

    Article  CAS  Google Scholar 

  • Largo C, Cuevas P, Somjen GG, Martin del Rio R, Herreras O (1996) The effect of depressing glial function in rat brain in situ on ion homeostasis, synaptic transmission, and neuron survival. J Neurosci 16:1219–1296

    CAS  Google Scholar 

  • Liao SL, Chen CJ (2001) Tyrosine kinase signaling involved in glutamate-induced astrocyte proliferation. Neuroreport 12:3519–3522

    Article  CAS  Google Scholar 

  • Ling EA (1976) Study in the changes of the proportions and numbers of the various glial cell types in the spinal cord of neonatal and young adult rats. Acta Anat 96:188–195

    Article  CAS  Google Scholar 

  • Mcdermott KW, Barry DS, Mcmahon SS (2005) Role of radial glia in cytogenesis patterning and boundary formation in the developing spinal cord. J Anat 207:241–250

    Article  Google Scholar 

  • Mi HY, Ben AB (1999) Purification and Characterization of Astrocyte Precursor Cells in the Developing Rat Optic Nerve. J Neurosci 19:1049–1061

    CAS  Google Scholar 

  • Miller S, Sehati N, Romano C, Cotman CM (1996) Exposure of astrocytes to thrombin reduces levels of the metabotropic glutamate receptor mGluR5. J Neurochem 67:1435–1447

    Article  CAS  Google Scholar 

  • Mosmann T (1983) Rapid colorimetric assay for cellular growth and survival application to proliferation and cytotoxic assay. J Immunol Methods 65:55–63

    Article  CAS  Google Scholar 

  • Phifer CB, Terry LM (1986) Use of hypothermia for general anesthesia in preweanling rodents. Physio Behav 38:887–890

    Article  CAS  Google Scholar 

  • Simpson DL, Morrison R, Velliis JD, Herschman HR (1982) Epidermal growth factor binding and mitogenic activity on purified population of cells from central nervous system. J Neurosci Res 8:453–462

    Article  CAS  Google Scholar 

  • Stahl B, Wiesinger H, Hamprecht B (1989) Characteristics of sorbitol uptake in rat glial primary cultures. J Neurochem 53:665–671

    Article  CAS  Google Scholar 

  • Travis J (1994) Glia: the brain’s other cells. Science 266:970–972

    Article  CAS  Google Scholar 

  • Valentino KL, Jones EG, Kane SA (1983) Expression of GFAP immunoreactivity during development of long fiber tracts in the rat CNS. Brain Res 285:317–336

    CAS  Google Scholar 

  • Walz W (1989) Role of glial cells in the regulation of the brain ion microenvironment. Prog Neurobiol 33:309–333

    Article  CAS  Google Scholar 

  • Walz W (1987) Swelling and potassium uptake in cultured astrocytes. Can J Physiol Pharmacol 65:1051–1057

    CAS  Google Scholar 

  • Warf BC, Fork-Seaning J, Miller RH (1991) Evidence for the ventral origin of oligodendrocyte precursors in the rat spinal cord. J Neurosci 11:2477–2488

    CAS  Google Scholar 

  • Wiesinger H, Schuricht B, Hamprecht B (1991) Replacement of glucose by sorbitol in growth medium causes selection of astroglial cells from heterogeneous primary cultures derived from newborn mouse brain. Brain Res 550:69–76

    Article  CAS  Google Scholar 

  • Wiesinger H, Thiess U, Hamprecht B (1990) Sorbitol pathway activity and utilization of polyols in astroglia-rich primary cultures. Glia 3:277–282

    Article  CAS  Google Scholar 

  • Zhang JM, Wang HK, Chang-quan YE, Ge WP, Wu CP, Poo MM, Duan SM (2003) ATP Released by astrocytes mediates glutamtergic activity-dependent heterosynaptic suppression. Neuron 40:971–982

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by the National Natural science foundation of China (30230450), Basic Research Program of China (2002CB515301).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gong Ju.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Yang, H., Liang, Z., Li, J. et al. Optimized and efficient preparation of astrocyte cultures from rat spinal cord. Cytotechnology 52, 87–97 (2006). https://doi.org/10.1007/s10616-006-9033-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10616-006-9033-4

Keywords

Navigation