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Injured adult motor and sensory axons regenerate into appropriate organotypic domains of neural progenitor grafts

Author

Listed:
  • Jennifer N. Dulin

    (University of California, San Diego)

  • Andrew F. Adler

    (University of California, San Diego)

  • Hiromi Kumamaru

    (University of California, San Diego)

  • Gunnar H. D. Poplawski

    (University of California, San Diego)

  • Corinne Lee-Kubli

    (University of California, San Diego)

  • Hans Strobl

    (University of California, San Diego)

  • Daniel Gibbs

    (University of California, San Diego)

  • Ken Kadoya

    (University of California, San Diego
    Hokkaido University)

  • James W. Fawcett

    (University of Cambridge)

  • Paul Lu

    (University of California, San Diego
    Veterans Administration Medical Center)

  • Mark H. Tuszynski

    (University of California, San Diego
    Veterans Administration Medical Center)

Abstract

Neural progenitor cell (NPC) transplantation has high therapeutic potential in neurological disorders. Functional restoration may depend on the formation of reciprocal connections between host and graft. While it has been reported that axons extending out of neural grafts in the brain form contacts onto phenotypically appropriate host target regions, it is not known whether adult, injured host axons regenerating into NPC grafts also form appropriate connections. We report that spinal cord NPCs grafted into the injured adult rat spinal cord self-assemble organotypic, dorsal horn-like domains. These clusters are extensively innervated by regenerating adult host sensory axons and are avoided by corticospinal axons. Moreover, host axon regeneration into grafts increases significantly after enrichment with appropriate neuronal targets. Together, these findings demonstrate that injured adult axons retain the ability to recognize appropriate targets and avoid inappropriate targets within neural progenitor grafts, suggesting that restoration of complex circuitry after SCI may be achievable.

Suggested Citation

  • Jennifer N. Dulin & Andrew F. Adler & Hiromi Kumamaru & Gunnar H. D. Poplawski & Corinne Lee-Kubli & Hans Strobl & Daniel Gibbs & Ken Kadoya & James W. Fawcett & Paul Lu & Mark H. Tuszynski, 2018. "Injured adult motor and sensory axons regenerate into appropriate organotypic domains of neural progenitor grafts," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-017-02613-x
    DOI: 10.1038/s41467-017-02613-x
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    Cited by:

    1. T. M. O’Shea & Y. Ao & S. Wang & A. L. Wollenberg & J. H. Kim & R. A. Ramos Espinoza & A. Czechanski & L. G. Reinholdt & T. J. Deming & M. V. Sofroniew, 2022. "Lesion environments direct transplanted neural progenitors towards a wound repair astroglial phenotype in mice," Nature Communications, Nature, vol. 13(1), pages 1-22, December.
    2. Michael Pitonak & Miriam Aceves & Prakruthi Amar Kumar & Gabrielle Dampf & Peyton Green & Ashley Tucker & Valerie Dietz & Diego Miranda & Sunjay Letchuman & Michelle M. Jonika & David Bautista & Heath, 2022. "Effects of biological sex mismatch on neural progenitor cell transplantation for spinal cord injury in mice," Nature Communications, Nature, vol. 13(1), pages 1-12, December.

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