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Survival and function of aggregate cultures of rat fetal dopamine neurons grafted in a rat model of Parkinson's disease

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Summary

The ability to maintain tissue in culture prior to grafting would greatly facilitate the widespread application of graft therapy to neurological diseases such as Parkinson's disease. However, neurons cultured on planar substrata can be easily damaged when they are removed from the substrata and redissociated for use in grafting procedures. To overcome this limitation we utilized aggregate tissue culture methods, which allowed dopamine (DA)-rich neuronal tissue to be grafted directly following culture, without an additional redissociation. Fetal rat dopamine-neuron-containing ventral mesencephalon was cultured for 9 days in rotating flasks. The cells formed many small spheres (280 μm mean diameter), each estimated to contain about 10000 cells. Forty such aggregate spheres were injected via a 22G needle into the DA-denervated striata of host Parkinsonian rats. A significant reduction of amphetamine-induced rotation was seen onward from 6 weeks post-transplantation, with a complete reversal of rotational asymmetry by 15 weeks post-transplantation. Well placed, surviving grafts were found in all behaviorally compensated rats (N = 6). Grafts contained an average of 517 tyrosine hydroxylase (TH)-positive neurons, as well as TH-positive fibers seen extending into the host striatum. These results suggest that aggregate culture methods are a promising means to maintain and deliver tissue for transplant therapy.

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References

  • Abercrombie M (1946) Estimation of nuclear population from microtome sections. Anat Rec 94:239–247

    Google Scholar 

  • Aebischer P, Winn SR, Galletti PM (1988) Transplantation of neural tissue in polymer capsules. Brain Res 448:364–368

    Google Scholar 

  • Aitken AR (1987) The preparation and use of embryonic brain wholemounts. J Neurosci Meth 19:297–304

    Google Scholar 

  • Björklund A, Stenevi U (1979) Reconstruction of the nigrostriatal pathway by intracerebral nigral transplants. Brain Res 177:555–560

    Google Scholar 

  • Björklund A, Stenevi U, Schmidt RH, Dunnett SB, Gage FH (1983) Intracerebral grafting of neuronal cell suspensions. I. Introduction and general methods of preparation. Acta Physiol Scand Suppl 522:1–7

    Google Scholar 

  • Brundin P, Barbin G, Isacson O, Mallat M, Chamak B, Prochiantz A, Gage FH, Björklund A (1985) Survival of intracerebrally grafted rat dopamine neurons previously cultured in vitro. Neurosci Lett 61:79–84

    Google Scholar 

  • Brundin P, Björklund A (1987) Survival, growth and function of dopaminergic neurons grafted to the brain. In: Seil FJ, Herbert E, Carlson B (eds) Progress in brain research Vol 71. Elsevier, North Holland, pp 293–308

    Google Scholar 

  • Brundin P, Barbin G, Strecker RE, Isacson O, Prochiantz A, Björklund A (1988) Survival and function of dissociated rat dopamine neurones grafted at different developmental stages or after being cultured in vitro. Dev Brain Res 39:233–243

    Google Scholar 

  • Colombo JA, Almeida JI, Molina S (1987) In vitro culture and labeling of neural cell aggregates followed by transplantation. Exp Neurol 98:606–615

    Google Scholar 

  • DeLong GR (1970) Histogenesis of fetal mouse isocortex and hippocampus in reaggregating cell cultures. Dev Biol 22:563–583

    Google Scholar 

  • di Porzio U, Rougon G, Novotny EA, Barker JL (1987) Dopaminergic neurons from the embryonic mouse mesencephalon are enriched in culture through immunoreaction with monoclonal antibody to neural specific protein 4 and flow cytometry. Proc Natl Acad Sci 84:7334–7338

    Google Scholar 

  • Doering LC, Fedoroff S (1982) Isolation and identification of neuroblast precursor cells from mouse neopallium. Dev Brain Res 5:229–233

    Google Scholar 

  • Garber BB, Moscona AA (1972) Reconstruction of brain tissue from cell suspensions. I. Aggregation patterns of cells dissociated from different regions of the developing brain. Dev Biol 27:217–234

    Google Scholar 

  • Gibbs RB, Pixley SKR, Cotman CW (1986) Transplantation of septal neurons maintained in long-term culture. Brain Res 382:409–415

    Google Scholar 

  • Goldberg WJ, Bernstein JJ (1987) Transplant-derived astrocytes migrate into host lumbar and cervical spinal cord after implantation of E14 fetal cerebral cortex into adult thoracic spinal cord. J Neurosci Res 17:391–403

    Google Scholar 

  • Hemmendinger LM, Garber BB, Hoffmann PC, Heller A (1981a) Selective association of embryonic murine mesencephalic dopamine neurons in vitro. Brain Res 222:417–422

    Google Scholar 

  • Hemmendinger LM, Garber BB, Hoffmann PC, Heller A (1981b) Target neuron-specific process formation by embryonic mesencephalic dopamine neurons in vitro. Proc Natl Acad Sci 78:1264–1268

    CAS  PubMed  Google Scholar 

  • Honegger P, Richelson E (1977) Biochemical differentiation of aggregating cell cultures of different fetal rat brain regions. Brain Res 133:329–339

    Google Scholar 

  • Hoffmann PC, Hemmendinger LM, Kotake C, Heller A (1983) Enhanced dopamine cell survival in reaggregates containing telencephalic target cells. Brain Res 274:275–281

    Article  CAS  PubMed  Google Scholar 

  • Kamo H, Kim SU, McGeer PL, Shin DH (1986) Functional recovery in a rat model of Parkinson's disease following transplantation of cultured human sympathetic neurons. Brain Res 397:372–376

    Google Scholar 

  • Kotake C, Hoffmann PC, Heller A (1982) The biochemical and morphological development of differentiating dopamine neurons coaggregated with their target cells of the corpus striatum in vitro. J Neurosci 2:1307–1315

    Google Scholar 

  • Lindsay RM, Raisman G, Seeley PJ (1987) Intracerebral transplantation of cultured neurons after reaggregation in a plasma clot. Neuroscience 21:685

    Google Scholar 

  • Loring JF, Erickson CA (1987) Neural crest cell migratory pathways in the trunk of the chick embryo. Dev Biol 121:220–236

    Google Scholar 

  • Marsden CD, Parkes JD (1977) Success and problems of longterm levodopa therapy in Parkinson's disease. Lancet 1:345–349

    Google Scholar 

  • Perlow MJ, Freed WJ, Hoffer BJ, Seiger Å, Olson L, Wyatt RJ (1979) Brain grafts reduce motor abnormalities produced by destruction of nigrostriatal dopamine system. Science 204:643–647

    Google Scholar 

  • Prochiantz A, di Porzio U, Kato A, Berger B, Glowinski J (1979) In vitro maturation of mesencephalic dopaminergic neurons from mouse embryos is enhanced in presence of their striatal target cells. Proc Natl Acad Sci USA 76:5387–5391

    CAS  PubMed  Google Scholar 

  • Schmidt RH, Björklund A, Stenevi U, Dunnett SB, Gage FH (1983) Intracerebral grafting of neuronal cell suspensions. III. Activity of intrastriatal nigral suspension implants as assessed by measurements of dopamine synthesis and metabolism. Acta Physiol Scand (Suppl) 522:19–28

    Google Scholar 

  • Schmued LC, Fallon JH (1986) Fluoro-gold: a new fluorescent retrograde axonal tracer with numerous unique properties. Brain Res 377:147–154

    Google Scholar 

  • Seeds NW (1974) Differentiation of aggregating brain cell cultures. In: Sato G (ed) Tissue culture of the nervous system. Plenum, New York, pp 35–53

    Google Scholar 

  • Strecker RE, Sharp T, Brundin P, Zetterström T, Ungerstedt U, Björklund A (1987) Autoregulation of dopamine release and metabolism by intrastriatal nigral grafts as revealed by intracerebral dialysis. Neuroscience 22:169–178

    Google Scholar 

  • Trapp BD, Honegger P, Richelson E, Webster de FH (1979) Morphological differentiation of mechanically dissociated fetal rat brain in aggregating cell cultures. Brain Res 160:117–130

    Google Scholar 

  • Ungerstedt U, Arbuthnott GW (1970) Quantitative recording of rotational behavior in rats after 6-hydroxy-dopamine lesions of the nigrostriatal dopamine system. Brain Res 24:485–493

    Article  CAS  PubMed  Google Scholar 

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Strecker, R.E., Miao, R. & Loring, J.F. Survival and function of aggregate cultures of rat fetal dopamine neurons grafted in a rat model of Parkinson's disease. Exp Brain Res 76, 315–322 (1989). https://doi.org/10.1007/BF00247891

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  • DOI: https://doi.org/10.1007/BF00247891

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