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Excoffier, B.

Publications and source records attributed to Excoffier, B..

2 recordsLinked to original sources

Axon guidance during CNS regeneration is required for specific brain innervation

Reconstruction of functional neuronal circuits in the mature brain remains a big challenge in the field of central nervous system (CNS) repair. Despite achievement of robust, long-distance regeneration through modulation of specific neuronal intrinsic growth properties, functional recovery is still limited due to major guidance defects of regenerating axons. Using co-activation of mTOR, JAK/STAT and c-myc pathways in retinal ganglion cells (RGC), we highlight that regenerating axons avoid the suprachiasmatic nucleus (SCN) due to repulsive mechanisms. We show that Slit/Robo guidance signaling is responsible for this reinnervation failure. In vivo suppression of this repulsive signaling allows regenerating axons to enter the SCN. The newly formed circuit is associated with functional behavioral recovery. Our results provide evidence that axon guidance mechanisms are required in the context of mature neuronal circuit repair.

neuroscience↗

The RSK-RPS6 axis controls the preconditioning effect and induces spinal cord regeneration

Unlike immature neurons and neurons from the peripheral nervous system (PNS), mature neurons from the central nervous system (CNS) cannot regenerate after injury. In the past 15 years, huge progress has been made to identify molecules and pathways necessary for neuroprotection and/or regeneration after CNS injury. In most regenerative models, phosphorylated ribosomal protein S6 (p-RPS6) is upregulated in neurons, which is often associated with an activation of the mTOR pathway. However, the exact contribution of post-translational modifications of this ribosomal protein in CNS regeneration remains elusive. In this study, we demonstrate that RPS6 phosphorylation is essential for PNS and CNS regeneration. We show that this phosphorylation is induced during the preconditioning effect in dorsal root ganglion (DRG) neurons, and that it is controlled by the p90S6 kinase RSK2. Our results reveal that RSK2 controls the preconditioning effect and that the RSK2-RPS6 axis is key for this process, as well as for PNS regeneration. Finally, we demonstrate that RSK2 promotes CNS regeneration in the dorsal column and allows functional recovery. Our data establish the critical role of RPS6 phosphorylation controlled by RSK2 in CNS regeneration and give new insights into the mechanism related to axon growth and circuit formation after traumatic lesion.

neuroscience↗