The Spinal Transcriptome after Cortical Stroke: In Search of Molecular Factors Regulating Spontaneous Recovery in the Spinal Cord

• Published in: The Journal of neuroscience Vol. 39; no. 24; pp. 4714 - 4726
• Main Authors: Kaiser, Julia, Maibach, Martina, Salpeter, Iris, Hagenbuch, Niels, de Souza, Vladimir B C, Robinson, Mark D, Schwab, Martin E
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 12-06-2019
• Subjects: Axon sprouting; Axonogenesis; Axons; Biological activity; Complement activation; Cortex (motor); Degeneration; Fibers; Gene expression; Gene sequencing; Genes; Genomes; Inflammation; Injuries; Ischemia; Laminates; Mice; Microglia; Molecular modelling; Phagocytes; Pyramidal tracts; Recovery; Reinnervation; Rodents; Spinal cord; Spinal cord injuries; Spontaneous recovery; Stroke; Substantia grisea; plasticity; recovery; spinal cord; regeneration; stroke; transcriptome
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.2571-18.2019

In response to cortical stroke and unilateral corticospinal tract degeneration, compensatory sprouting of spared corticospinal fibers is associated with recovery of skilled movement in rodents. To date, little is known about the molecular mechanisms orchestrating this spontaneous rewiring. In this study, we provide insights into the molecular changes in the spinal cord tissue after large ischemic cortical injury in adult female mice, with a focus on factors that might influence the reinnervation process by contralesional corticospinal neurons. We mapped the area of cervical gray matter reinnervation by sprouting contralesional corticospinal axons after unilateral photothrombotic stroke of the motor cortex in mice using anterograde tracing. The mRNA profile of this reinnervation area was analyzed using whole-genome sequencing to identify differentially expressed genes at selected time points during the recovery process. Bioinformatic analysis revealed two phases of processes: early after stroke (4-7 d post-injury), the spinal transcriptome is characterized by inflammatory processes, including phagocytic processes as well as complement cascade activation. Microglia are specifically activated in the denervated corticospinal projection fields in this early phase. In a later phase (28-42 d post-injury), biological processes include tissue repair pathways with upregulated genes related to neurite outgrowth. Thus, the stroke-denervated spinal gray matter, in particular its intermediate laminae, represents a growth-promoting environment for sprouting corticospinal fibers originating from the contralesional motor cortex. This dataset provides a solid starting point for future studies addressing key elements of the post-stroke recovery process, with the goal to improve neuroregenerative treatment options for stroke patients.
We show that the molecular changes in the spinal cord target tissue of the stroke-affected corticospinal tract are mainly defined by two phases: an early inflammatory phase during which microglia are specifically activated in the target area of reinnervating corticospinal motor neurons; and a late phase during which growth-promoting factors are upregulated which can influence the sprouting response, arborization, and synapse formation. By defining for the first time the endogenous molecular machinery in the stroke-denervated cervical spinal gray matter with a focus on promotors of axon growth through the growth-inhibitory adult CNS, this study will serve as a basis to address novel neuroregenerative treatment options for chronic stroke patients.