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Functional integration of striatal allografts in a primate model of Huntington's disease

Abstract

Huntington's disease is an autosomal dominant, inherited disorder that results in progressive degeneration of the basal ganglia (especially the neostriatal caudate nucleus and putamen) and other forebrain structures and is associated with a clinical profile of movement, cognitive and psychiatric impairments for which there is at present no effective therapy1. Neuropathological, neurochemical and behavioral features of the disease can all be reproduced in experimental animals by local injection of excito-toxic2,3 or metabolic4,5 toxins into the neostriatum. All these features of the disease can be alleviated, at least in rats, by transplantation of embryonic striatal tissue into the degenerated striatum6–8, which was the basis for commencing the first clinical trials of striatal transplantation in Huntington's patients9,10. However, although rat striatal xenografts may temporarily reduce apomorphine-induced dyskinesias in monkeys11, there has been no demonstration that allograft techniques that work well in rats translate effectively to the much larger differentiated striatum of primates12. Here we demonstrate good survival, differentiation and integration of striatal allografts in the primate neostriatum, and recovery in a test of skilled motor performance. Long-term graft survival in primates indicates probable success for clinical transplants in Huntington's disease; in addition, our data suggest that graft placement has a direct influence on the pattern and extent of functional recovery.

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References

  1. Harper, P.S. In Huntington's Disease (W.B. Saunders, London, 1996).

    Google Scholar 

  2. Coyle, J.T. & Schwarcz, R. Lesions of striatal neurones with kainic acid provides a model for Huntington's chorea. Nature 263, 244–246 (1976).

    Article  CAS  Google Scholar 

  3. Ferrante, R.J., Kowall, N.W., Cipolloni, P.B., Storey, E. & Beal, M.F. Excitotoxin lesions in primates as a model for Huntington's disease: Histopathologic and neuro-chemical characterization. Exp. Neurol. 119, 46–71 (1993).

    Article  CAS  Google Scholar 

  4. Beal, M.F. et al. Neurochemical and histologic characterization of striatal excito-toxic lesions produced by the mitochondrial toxin 3-nitropropionic acid. J. Neurosci. 13, 4181–4192 (1993).

    Article  CAS  Google Scholar 

  5. Palfi, S.P. et al. Chronic 3-nitropropionic acid treatment in baboons replicates the cognitive and motor deficits of Huntington's disease. J. Neurosci. 16, 3019–3025 (1996).

    Article  CAS  Google Scholar 

  6. Björklund, A., Campbell, K., Sirinathsinghji, D.J.S., Fricker, R.A. & Dunnett, S.B., In Functional Neural Transplantation, (eds Dunnett, S.B. & Björklund, A.) 157–195 (Raven Press, New York, 1994)

    Google Scholar 

  7. Dunnett, S.B., Isacson, O., Sirinathsinghji, D.J.S., Clarke, D.J. & Björklund, A. Striatal grafts in rats with unilateral neostriatal lesions. III. Recovery from dopamine-dependent motor asymmetry and deficits in skilled paw reaching. Neuroscience 24, 813–820 (1988).

    Article  CAS  Google Scholar 

  8. Wictorin, K. Anatomy and connectivity of intrastriatal striatal transplants. Prog. Neurobiol. 38, 611–639 (1992).

    Article  CAS  Google Scholar 

  9. Philpott, L.M. et al. Neuropsychological functioning following fetal striatal transplantation in Huntington's chorea: Three case presentations. Cell Transplant. 6, 203–212 (1997).

    Article  CAS  Google Scholar 

  10. Madrazo, I., Franco-Bourland, R.E., Castrejon, H., Cuevas, C. & Ostrosky-Solis, F. Fetal striatal homotransplantation for Huntington's disease: First two case reports. Neurol. Res. 17, 312–315 (1995).

    Article  CAS  Google Scholar 

  11. Hantraye, P., Riche, D., Mazière, M. & Isacson, O. Intrastriatal transplantation of cross-species fetal striatal cells reduces abnormal movements in a primate model of Huntington's disease. Proc. Natl. Acad. Sci. USA 89, 4187–4191 (1992).

    Article  CAS  Google Scholar 

  12. Helm, G.A., Palmer, P.E., Simmons, N.E., DiPierro, C.C. & Bennett, J.P. Degeneration of long-term fetal neostriatal allografts in the Rhesus monkey: An electron microscopic study. Exp. Neurol. 123, 174–180 (1993).

    Article  CAS  Google Scholar 

  13. Marshall, J.W.B. & Ridley, R.M. Assessment of functional impairment following permanent middle cerebral artery occlusion in a nonhuman primate species. Neurodegeneration 5, 275–286 (1996).

    Article  CAS  Google Scholar 

  14. Annett, L.E. et al. Behavioural assessment of the effects of embryonic nigral grafts in marmosets with unilateral 6-OHDA lesions of the nigrostriatal pathway. Exp. Neurol. 125, 228–246 (1994).

    Article  CAS  Google Scholar 

  15. Graybiel, A.M. et al. Intrastriatal grafts derived from fetal striatal primordia. I. Phenotypy and modular organization. J. Neurosci. 9, 3250–3271 (1989).

    Article  CAS  Google Scholar 

  16. Ouimet, C.C., Miller, P.E., Hemmings, H.C., Walaas, S.I. & Creengard, P. DARPP-32, a dopamine- and adenosine-3′,5′-monophosphate-regulated phosphoprotein enriched in dopamine-innervated brain regions. J. Neurosci. 4, 111–124 (1984).

    Article  CAS  Google Scholar 

  17. Helm, G.A., Palmer, P.E., Simmons, N.E., DiPierro, C. & Bennett, J.P. Descriptive morphology of developing fetal neostriatal allografts in the rhesus monkey: A correlated light and electron microscopic golgi study. Neuroscience 50, 163–179 (1992).

    Article  CAS  Google Scholar 

  18. Isacson, O., Riche, D., Hantraye, P., Sofroniew, M.V. & Mazière, M. A primate model of Huntington's disease: Cross-species implantation of striatal precursor cells to the excitotoxically lesioned baboon caudate-putamen. Exp. Brain Res. 75, 213–220 (1989).

    Article  CAS  Google Scholar 

  19. Stephan, H., Baron, R. & Schwerdtfeger, W.K. In The Brain of the Common Marmoset: a Stereotaxic Atlas. (Springer-Verlag, Berlin, 1980).

    Google Scholar 

  20. Dunnett, S.B. & Björklund, A. Neural Transplantation: A Practical Approach. (IRL Press, Oxford, 1992).

    Google Scholar 

  21. Pakzaban, P., Deacon, T.W., Burns, L.H. & Isacson, O. Increased proportion of acetylcholinesterase-rich zones and improved morphological integration in host striatum of fetal grafts derived from the lateral but not the medial ganglionic eminence. Exp. Brain Res. 97, 13–22 (1993).

    Article  CAS  Google Scholar 

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Kendall, A., Rayment, F., Torres, E. et al. Functional integration of striatal allografts in a primate model of Huntington's disease. Nat Med 4, 727–729 (1998). https://doi.org/10.1038/nm0698-727

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