c-Jun Reprograms Schwann Cells of Injured Nerves to Generate a Repair Cell Essential for Regeneration

Peter Arthur‐Farraj(University College London), Morwena Latouche(University College London), Daniel K. Wilton(University College London), Susanne Quintes(University College London), Elodie Chabrol(University College London), Ambily Banerjee(University College London), Ashwin Woodhoo(CIC bioGUNE), Billy Jenkins(University College London), Mary Rahman(University College London), Mark Turmaine(University College London), Grzegorz Wicher(Uppsala University), Richard Mitter(The Honourable Society of Lincoln's Inn), Linda Greensmith(National Hospital for Neurology and Neurosurgery), Axel Behrens(The Honourable Society of Lincoln's Inn), Gennadij Raivich(University College London), Rhona Mirsky(University College London), Kristján R. Jessen(University College London)
Neuron
August 1, 2012
Cited by 855Open Access
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Abstract

The radical response of peripheral nerves to injury (Wallerian degeneration) is the cornerstone of nerve repair. We show that activation of the transcription factor c-Jun in Schwann cells is a global regulator of Wallerian degeneration. c-Jun governs major aspects of the injury response, determines the expression of trophic factors, adhesion molecules, the formation of regeneration tracks and myelin clearance and controls the distinctive regenerative potential of peripheral nerves. A key function of c-Jun is the activation of a repair program in Schwann cells and the creation of a cell specialized to support regeneration. We show that absence of c-Jun results in the formation of a dysfunctional repair cell, striking failure of functional recovery, and neuronal death. We conclude that a single glial transcription factor is essential for restoration of damaged nerves, acting to control the transdifferentiation of myelin and Remak Schwann cells to dedicated repair cells in damaged tissue.


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