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Transplanted embryonic stem cells survive, differentiate and promote recovery in injured rat spinal cord

Abstract

Transplantation approaches using cellular bridges1,2, fetal central nervous system cells3,4,5, fibroblasts expressing neurotrophin-3 (ref. 6), hybridoma cells expressing inhibitory protein-blocking antibodies7, or olfactory nerves ensheathing glial cells8 transplanted into the acutely injured spinal cord have produced axonal regrowth or functional benefits. Transplants of rat or cat fetal spinal cord tissue into the chronically injured cord survive and integrate with the host cord, and may be associated with some functional improvements9. In addition, rats transplanted with fetal spinal cord cells have shown improvements in some gait parameters10, and the delayed transplantation of fetal raphe cells can enhance reflexes11. We transplanted neural differentiated mouse embryonic stem cells into a rat spinal cord 9 days after traumatic injury. Histological analysis 2–5 weeks later showed that transplant-derived cells survived and differentiated into astrocytes, oligodendrocytes and neurons, and migrated as far as 8 mm away from the lesion edge. Furthermore, gait analysis demonstrated that transplanted rats showed hindlimb weight support and partial hindlimb coordination not found in 'sham-operated' controls or control rats transplanted with adult mouse neocortical cells.

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Figure 1: BrdU labeled ES cell-derived cells 2 weeks after transplantation.
Figure 2: Transplanted ES cell-derived cells differentiate into oligodendrocytes, astrocytes and neurons.
Figure 3: ES cell-derived cell transplantation improved behavioral recovery.

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References

  1. Richardson, P.M., McGuinness, U.M. & Aguayo, A.J. Axons from CNS neurones regenerate into PNS grafts. Nature 284, 264–265 (1980).

    Article  CAS  Google Scholar 

  2. Xu, X.M., Guenard, V., Kleitman, N. & Bunge, M.B. Axonal regeneration into Schwann cell-seeded guidance channels grafted into transected adult rat spinal cord. J. Comp. Neurol. 351, 145–160 (1995).

    Article  CAS  Google Scholar 

  3. Bernstein, J.J. & Goldberg, W.J. Fetal spinal cord homografts ameliorate the severity of lesion-induced hindlimb behavioral deficits. Exp. Neurol. 98, 633–644 (1987).

    Article  CAS  Google Scholar 

  4. Bregman, B.S. et al. Recovery of function after spinal cord injury: mechanisms underlying transplant- mediated recovery of function differ after spinal cord injury in newborn and adult rats. Exp. Neurol. 123, 3–16 (1993).

    Article  CAS  Google Scholar 

  5. Howland, D.R., Bregman, B.S., Tessler, A. & Goldberger M.E. Transplants enhance locomotion in neonatal kittens whose spinal cords are transected: a behavioral and anatomical study. Exp. Neurol. 135, 123–145 (1995).

    Article  CAS  Google Scholar 

  6. Grill, R., Murai, K., Blesch, A., Gage, F.H. & Tuszynski, M.H. Cellular delivery of neurotrophin-3 promotes corticospinal axonal growth and partial functional recovery after spinal cord injury. J. Neurosci. 17: 5560–5572 (1997).

    Article  CAS  Google Scholar 

  7. Schnell, L. & Schwab, M.E. Axonal regeneration in the rat spinal cord produced by an antibody against myelin-associated neurite outgrowth inhibitors. Nature 343, 269–272 (1990).

    Article  CAS  Google Scholar 

  8. Li, Y., Field, P.M. & Raisman, G. Repair of adult rat corticospinal tract by transplants of olfactory ensheathing cells. Science 227, 2000–2002 (1997).

    Article  Google Scholar 

  9. Anderson, D.K. et al. Transplants of fetal CNS grafts in chronic compression lesions of the adult cat spinal cord. Resor. Neurol. Neurosci. 2, 309–325 (1991).

    CAS  Google Scholar 

  10. Stokes, B.T. & Reier, P.J. Fetal grafts alter chronic behavioral outcome after contusion damage to the adult rat spinal cord. Exp. Neurol. 116, 1–12 (1992).

    Article  CAS  Google Scholar 

  11. Privat, A., Mansour, H., Rajaofetra, N. & Geffard, M. Intraspinal transplants of serotonergic neurons in the adult rat. Brain Res. Bull. 22, 123–129 (1989).

    Article  CAS  Google Scholar 

  12. Gage, F.H. et al. Survival and differentiation of adult neuronal progenitor cells transplanted to the adult brain. Proc. Natl. Acad. Sci. USA 92, 11879–11883 (1995).

    Article  CAS  Google Scholar 

  13. Dinsmore, J. et al. Embryonic stem cells differentiated in vitro as a novel source of cells for transplantation. Cell Transplant. 5, 131–143 (1996).

    Article  CAS  Google Scholar 

  14. Brustle, O. et al. In vitro-generated neural precursors participate in mammalian brain development. Proc. Natl. Acad. Sci. USA 94, 14809–14814 (1997).

    Article  CAS  Google Scholar 

  15. Basso, D.M., Beattie, M.S. & Bresnahan, J.C. A sensitive and reliable locomotor rating scale for open field testing in rats. J. Neurotrauma 12,1–21 (1995).

    Article  CAS  Google Scholar 

  16. Liu, X.Z. et al. Neuronal and glial apoptosis after traumatic spinal cord injury. J. Neurosci. 17, 5395–5406 (1997).

    Article  CAS  Google Scholar 

  17. Bain, G., Kitchens, D., Yao, M. & Gottlieb, D.I. Embryonic stem cells express neuronal properties in vitro. Dev. Biol. 168, 342–357 (1995).

    Article  CAS  Google Scholar 

  18. Lagenaur, C. & Schachner, M. Monoclonal antibody (M2) to glial and neuronal cell surfaces. J. Supramol. Struct. Cell Biochem. 15, 335–346 (1981).

    Article  CAS  Google Scholar 

  19. Baumrind, N.L., Parkinson, D., Wayne, D.B., Heuser, J.E. & Pearlman, A.L. EMA: a developmentally regulated cell-surface glycoprotein of CNS neurons that is concentrated at the leading edge of growth cones. Dev. Dyn. 194, 311–325 (1992).

    Article  CAS  Google Scholar 

  20. Waxman, S.G. Demyelination in spinal cord injury and multiple sclerosis: What can we do to enhance functional recovery? J. Neurotrauma 9, s105–s117 (1992).

    PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by National Institutes of Health grants NS01931, NS37927 (J.W.M.), NS32636 (D.W.C.) and RR-12309 (D.I.G.); the Alan A. and Edith L. Wolff Charitable Trust (D.I.G.); the Christopher Reeve Paralysis Foundation (J.W.M. and D.W.C.); and the Keck Foundation (J.W.M., D.W.C. and D.I.G.).

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Correspondence to John W. McDonald.

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McDonald, J., Liu, XZ., Qu, Y. et al. Transplanted embryonic stem cells survive, differentiate and promote recovery in injured rat spinal cord. Nat Med 5, 1410–1412 (1999). https://doi.org/10.1038/70986

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