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Cell biology of spinal cord injury and repair
Timothy M. O’Shea, Joshua E. Burda, Michael V. Sofroniew
Timothy M. O’Shea, Joshua E. Burda, Michael V. Sofroniew
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Cell biology of spinal cord injury and repair

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Abstract

Spinal cord injury (SCI) lesions present diverse challenges for repair strategies. Anatomically complete injuries require restoration of neural connectivity across lesions. Anatomically incomplete injuries may benefit from augmentation of spontaneous circuit reorganization. Here, we review SCI cell biology, which varies considerably across three different lesion-related tissue compartments: (a) non-neural lesion core, (b) astrocyte scar border, and (c) surrounding spared but reactive neural tissue. After SCI, axon growth and circuit reorganization are determined by neuron-cell-autonomous mechanisms and by interactions among neurons, glia, and immune and other cells. These interactions are shaped by both the presence and the absence of growth-modulating molecules, which vary markedly in different lesion compartments. The emerging understanding of how SCI cell biology differs across lesion compartments is fundamental to developing rationally targeted repair strategies.

Authors

Timothy M. O’Shea, Joshua E. Burda, Michael V. Sofroniew

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Figure 2

Circuits reorganize after SCI.

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Circuits reorganize after SCI.
(A) Different types of circuit reorganiza...
(A) Different types of circuit reorganization after different types of SCI. Anatomically complete SCI is associated with synaptic plasticity that can give rise to maladaptive effects such as muscle spasticity or autonomic dysreflexia. Anatomically incomplete SCI can also give rise to axon growth and synaptic plasticity that can partially restore function. (B) Different potential growth responses of axons and synapses after SCI. DMo, descending motor projections.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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