Sustained MAPK/ERK activation in adult Schwann cells impairs nerve repair

Journal article

The MAPK/ERK pathway has a critical role in PNS development. It is required for Schwann cell (SC) differentiation and myelination; sustained embryonic MAPK/ERK activation in SCs enhances myelin growth overcoming signals that normally end myelination. Excess activation of this pathway can be maladaptive as in adulthood acute strong activation of MAPK/ERK has been shown to cause SC dedifferentiation and demyelination. We used a mouse model (including male and female animals) in which gain of function Mek1DD allele produces sustained MAPK/ERK activation in adult SCs and we determined the impact of such activation on nerve repair. In the uninjured nerve, MAPK/ERK activation neither impaired myelin nor did it re-activate myelination. However, in the injured nerve it was detrimental and resulted in delayed repair and functional recovery. In the early phase of injury the rate of myelin clearance was faster. Four weeks following injury, when nerve repair is normally advanced, myelinated axons of Mek1DD mutants demonstrated higher rates of myelin decompaction, a reduced number of Cajal bands and decreased internodal length. We noted the presence of abnormal Remak bundles with long SCs processes and reduced numbers of C-fibres/Remak bundle. Both the total number of regenerating axons and the intra-epidermal nerve fibres density in the skin were reduced. Sustained activation of MAPK/ERK in adult SCs is therefore deleterious to successful nerve repair, emphasising the differences in the signalling processes coordinating nerve development and repair. Our results also underline the key role of SCs in axon regeneration and successful target reinnervation.

Authors: Cervellini, I; Galino, J; Zhu, N; Allen, S; Birchmeier, C

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Society for Neuroscience
• Journal: Journal of Neuroscience
• Volume: 38
• Issue: 3
• Pages: 679-690
• Publication date: 2017-12-07
• Acceptance date: 2017-10-19
• DOI: 10.1523/JNEUROSCI.2255-17.2017
• EISSN: 1529-2401
• ISSN: 0270-6474