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.

Details

Title
Injured adult motor and sensory axons regenerate into appropriate organotypic domains of neural progenitor grafts
Author
Dulin, Jennifer N 1   VIAFID ORCID Logo  ; Adler, Andrew F 1 ; Kumamaru, Hiromi 1 ; Poplawski, Gunnar H D 1 ; Lee-Kubli, Corinne 1 ; Strobl, Hans 1 ; Gibbs, Daniel 1 ; Kadoya, Ken 2 ; Fawcett, James W 3 ; Lu, Paul 4 ; Tuszynski, Mark H 4 

 Department of Neurosciences, University of California, San Diego, La Jolla, CA, USA 
 Department of Neurosciences, University of California, San Diego, La Jolla, CA, USA; Department of Orthopaedic Surgery, Hokkaido University, Sapporo, Japan 
 John van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK 
 Department of Neurosciences, University of California, San Diego, La Jolla, CA, USA; Veterans Administration Medical Center, San Diego, CA, USA 
First page
1
Publication year
2018
Publication date
Jan 2018
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1985579029
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.