Spared corticospinal neurons activate an endogenous plasticity program after partial CNS injury
- 1Yale University
Abstract
Functional recovery after incomplete spinal cord injury depends substantially on the capacity of anatomically spared neurons to remodel their connections, yet the molecular programs underlying this endogenous plasticity remain poorly understood. To identify and validate these mechanisms, we combined retrograde labeling, unilateral corticospinal tract injury, and spatial transcriptomics in mice, with an in vitro human neuron model of neurite regeneration. Injured corticospinal neurons (CSNs) exhibited widespread transcriptional downregulation; the few activated pathways included stress, cell death, and degenerative programs. In contrast, spared CSNs activated a coordinated pro-plasticity program characterized by metabolic, immune, and cytoskeletal remodeling together with suppression of axon growth-inhibitory signaling. Computational network and drug perturbation analyses identified, and human neuronal experiments validated, ARHGEF12 suppression and the histone deacetylase inhibitor (HDAC) vorinostat as complementary target- and state-based strategies to enhance neurite regeneration. These findings define key components of endogenous plasticity and provide a framework for discovering neural repair targets.
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BibTeX
@misc{murillo2026spared,
title = {{Spared corticospinal neurons activate an endogenous plasticity program after partial CNS injury}},
author = {M. Murillo and C. F. O'Brien and N. Golan and E. X. Yin and K. Brennand and W. B. Cafferty},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.08.750239},
url = {https://www.biorxiv.org/content/10.64898/2026.09.08.750239v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - Spared corticospinal neurons activate an endogenous plasticity program after partial CNS injury
AU - M. Murillo
AU - C. F. O'Brien
AU - N. Golan
AU - E. X. Yin
AU - K. Brennand
AU - W. B. Cafferty
PY - 2026
DA - 2026/09/08
PB - bioRxiv
DO - 10.64898/2026.09.08.750239
UR - https://www.biorxiv.org/content/10.64898/2026.09.08.750239v1
AB - Functional recovery after incomplete spinal cord injury depends substantially on the capacity of anatomically spared neurons to remodel their connections, yet the molecular programs underlying this endogenous plasticity remain poorly understood. To identify and validate these mechanisms, we combined retrograde labeling, unilateral corticospinal tract injury, and spatial transcriptomics in mice, with an in vitro human neuron model of neurite regeneration. Injured corticospinal neurons (CSNs) exhibited widespread transcriptional downregulation; the few activated pathways included stress, cell death, and degenerative programs. In contrast, spared CSNs activated a coordinated pro-plasticity program characterized by metabolic, immune, and cytoskeletal remodeling together with suppression of axon growth-inhibitory signaling. Computational network and drug perturbation analyses identified, and human neuronal experiments validated, ARHGEF12 suppression and the histone deacetylase inhibitor (HDAC) vorinostat as complementary target- and state-based strategies to enhance neurite regeneration. These findings define key components of endogenous plasticity and provide a framework for discovering neural repair targets.
ER -