Genetic or transcranial magnetic stimulation of B-RAF-MEK signaling promotes CST axon sprouting and functional regeneration
Francesco BoatoiD, Xiaofei GuaniD, Yanjie Zhu, Youngjae RyuiD, Mariel VoutounouiD, Christopher RynneiD, Chase R. FreschliniD, Paul ZumboiD, Doron BeteliD, Katherine S. MathoiD, Sergey N. Makarov, Zhuhao WuiD, Young‐Jin SoniD, Aapo R. NummenmaaiD, Z. Josh HuangiD, Dylan J. EdwardsiD, Jian ZhongiD
Abstract
Facilitating axon regeneration in the injured central nervous system remains a challenging task. RAF-MEK signaling plays an important role in axon elongation during nervous system development. Here we show that activation of B-RAF in mature corticospinal neurons elicited the expression of a discrete set of transcription factors previously implicated in the regeneration of zebrafish optic nerve axons. Genetic activation of B-RAF-MEK signaling promoted robust regeneration and sprouting of corticospinal tract axons after injury. Newly sprouting axon collaterals formed synaptic connections with spinal interneurons, correlating with the recovery of skilled motor function. Seeking a non-invasive way to stimulate axon regeneration, we found that suprathreshold high-frequency repetitive transcranial magnetic stimulation activates the B-RAF canonical effectors MEK1/2 and requires MEK1/2 activity to promote corticospinal axon regeneration and sprouting after injury. These data demonstrate a central role of neuron-intrinsic RAF-MEK signaling in enhancing the growth capacity of mature corticospinal neurons and propose HF-rTMS as a potential therapy for spinal cord injury. One Sentence SummaryGenetic or HF-rTMS-mediated activation of B-RAF- MEK signaling promotes CST axon sprouting and functional regeneration after a spinal cord injury.
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