Author
Listed:
- Maria Teresa Dell’Anno
(Yale School of Medicine
Yale School of Medicine)
- Xingxing Wang
(Yale School of Medicine
Yale School of Medicine)
- Marco Onorati
(University of Pisa
Yale School of Medicine)
- Mingfeng Li
(Yale School of Medicine)
- Francesca Talpo
(Yale School of Medicine)
- Yuichi Sekine
(Yale School of Medicine
Yale School of Medicine)
- Shaojie Ma
(Yale School of Medicine)
- Fuchen Liu
(Yale School of Medicine)
- William B. J. Cafferty
(Yale School of Medicine)
- Nenad Sestan
(Yale School of Medicine
Yale School of Medicine
Yale School of Medicine)
- Stephen M. Strittmatter
(Yale School of Medicine
Yale School of Medicine
Yale School of Medicine)
Abstract
Traumatic spinal cord injury results in persistent disability due to disconnection of surviving neural elements. Neural stem cell transplantation has been proposed as a therapeutic option, but optimal cell type and mechanistic aspects remain poorly defined. Here, we describe robust engraftment into lesioned immunodeficient mice of human neuroepithelial stem cells derived from the developing spinal cord and maintained in self-renewing adherent conditions for long periods. Extensive elongation of both graft and host axons occurs. Improved functional recovery after transplantation depends on neural relay function through the grafted neurons, requires the matching of neural identity to the anatomical site of injury, and is accompanied by expression of specific marker proteins. Thus, human neuroepithelial stem cells may provide an anatomically specific relay function for spinal cord injury recovery.
Suggested Citation
Maria Teresa Dell’Anno & Xingxing Wang & Marco Onorati & Mingfeng Li & Francesca Talpo & Yuichi Sekine & Shaojie Ma & Fuchen Liu & William B. J. Cafferty & Nenad Sestan & Stephen M. Strittmatter, 2018.
"Human neuroepithelial stem cell regional specificity enables spinal cord repair through a relay circuit,"
Nature Communications, Nature, vol. 9(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05844-8
DOI: 10.1038/s41467-018-05844-8
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