Injured adult motor and sensory axons regenerate into appropriate organotypic domains of neural progenitor grafts.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29311559.
- Also identified by DOI 10.1038/s41467-017-02613-x and PMC identifier 5758751.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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.
Medical subject headings
- Axons
- Motor Neurons
- Nerve Regeneration
- Neural Stem Cells
- Sensory Receptor Cells
- Spinal Cord Dorsal Horn
- Spinal Cord Injuries