4.8 Article

The neurons that restore walking after paralysis

期刊

NATURE
卷 611, 期 7936, 页码 540-+

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41586-022-05385-7

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资金

  1. Defitech Foundation
  2. Rolex for Enterprise
  3. Carigest Promex
  4. Wings for Life
  5. Riders4Riders
  6. ALARME
  7. Panacee Foundation
  8. Pictet Group Charitable Foundation
  9. Firmenich Foundation
  10. Bertarelli Foundation
  11. International Foundation for Research in Paraplegia
  12. ONWARD medical
  13. Swiss National Science Foundation (National Centre of Competence in Research in Robotics) [51NF40_185543, 310030_192558]
  14. InnoSuisse STIMO Bridge [41871.1 IP-LS]
  15. Eurostars [E!12743, E!113969]
  16. Swiss National Science Foundation [32003BE_205563]
  17. European Research Council (ERC) [682999, 842578, 665667]
  18. Human Frontiers in Science Program long-term fellowship [LT001278/2017-L]
  19. Swiss National Supercomputing Center (CSCS)
  20. Intramural Research Program of the NIH, NINDS
  21. Wings for Life Spinal Cord Research Foundation
  22. Gene Expression Core Facility at the School of Life Sciences of EPFL
  23. European Research Council (ERC) [682999] Funding Source: European Research Council (ERC)
  24. Swiss National Science Foundation (SNF) [32003BE_205563, 310030_192558] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

For patients with chronic spinal cord injury, walking ability was restored through spatiotemporal epidural electrical stimulation (EESREHAB). By analyzing mice models, a specific population of neurons necessary for walking recovery with EES after spinal cord injury was identified.
A spinal cord injury interrupts pathways from the brain and brainstem that project to the lumbar spinal cord, leading to paralysis. Here we show that spatiotemporal epidural electrical stimulation (EES) of the lumbar spinal cord(1-3) applied during neurorehabilitation(4,5) (EESREHAB) restored walking in nine individuals with chronic spinal cord injury. This recovery involved a reduction in neuronal activity in the lumbar spinal cord of humans during walking. We hypothesized that this unexpected reduction reflects activity-dependent selection of specific neuronal subpopulations that become essential for a patient to walk after spinal cord injury. To identify these putative neurons, we modelled the technological and therapeutic features underlying EES(REHAB )in mice. We applied single-nucleus RNA sequencing(6-9) and spatial transcriptomics(10,11) to the spinal cords of these mice to chart a spatially resolved molecular atlas of recovery from paralysis. We then employed cell type(12,13) and spatial prioritization to identify the neurons involved in the recovery of walking.A single population of excitatory interneurons nested within intermediate laminae emerged. Although these neurons are not required for walking before spinal cord injury, we demonstrate that they are essential for the recovery of walking with EES following spinal cord injury. Augmenting the activity of these neurons phenocopied the recovery of walking enabled by EESREHAB, whereas ablating them prevented the recovery of walking that occurs spontaneously after moderate spinal cord injury. We thus identified a recovery-organizing neuronal subpopulation that is necessary and sufficient to regain walking after paralysis. Moreover, our methodology establishes a framework for using molecular cartography to identify the neurons that produce complex behaviours.

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