ASN NEURO, 2025 · DOI: https://doi.org/10.1080/17590914.2024.2440299 · Published: January 1, 2025
Functional recovery following spinal cord injury will require the regeneration and repair of damaged neuronal pathways. It is well known that the tissue response to injury involves inflammation and the formation of a glial scar at the lesion site, which significantly impairs the capacity for neuronal regeneration and functional recovery. There are initial attempts by both supraspinal and intraspinal neurons to regenerate damaged axons, often influenced by the neighboring tissue pathology. Many experimental therapeutic strategies are targeted to further stimulate the initial axonal regrowth, with little consideration for the diversity of the affected neuronal populations. Neurons are not homogenous but instead exhibit a wide array of diversity in their gene expression, physiology, and intrinsic responses to injury. Understanding this diverse intrinsic response is crucial, as complete functional recovery requires the successful coordinated regeneration and reorganization of various neuron pathways.
Understanding neuronal diversity can lead to tailored treatments that target specific neuronal populations affected by SCI.
Considering the distance between the cell body and the injury site can optimize regenerative responses while minimizing neuronal death.
Stimulating the formation of new bypass circuits involving multiple neuronal populations can promote functional recovery.