BMC Neuroscience, 2019 · DOI: https://doi.org/10.1186/s12868-019-0491-y · Published: March 5, 2019
The spinal cord has a limited ability to repair itself after injury. However, propriospinal (PS) neurons have shown some capacity for axonal regeneration after spinal cord injury, regrowing and re-establishing connections across a spinal lesion. This study examines how the distance of the injury from the cell body of long descending propriospinal tract (LDPT) neurons affects their molecular response to injury, comparing it to the response of short thoracic propriospinal (TPS) neurons. The location of axonal injury relative to the neuron's cell body significantly impacts its regenerative response. The study suggests inherent differences between LDPT and TPS neurons affect their response to axotomy, implying different therapies may be needed to maximize regeneration of all PS axons after spinal cord injury.
Identifies potential gene targets for therapies aimed at promoting regeneration after spinal cord injury.
Suggests that different or multiple therapies may be needed to stimulate maximal regeneration of all propriospinal axons, recognizing the differences between neuronal populations.
Provides insights into why thoracic propriospinal neurons are involved in recovery of function even with the failure of supraspinal axon regeneration.