Sox2 expression in Schwann cells inhibits myelination in vivo and induces influx of macrophages to the nerve

Author:

Roberts Sheridan L.1,Dun Xin-peng1ORCID,Doddrell Robin D. S.1ORCID,Mindos Thomas1,Drake Louisa K.2ORCID,Onaitis Mark W.3,Florio Francesca4,Quattrini Angelo4,D'Antonio Maurizio4,Parkinson David B.1ORCID

Affiliation:

1. Plymouth University Peninsula Schools of Medicine and Dentistry, John Bull Building, Plymouth Science Park, Plymouth, PL6 8BU, UK

2. University of Bath, Bath BA2 7AY, England, UK

3. Dept. of Thoracic Surgery, University of California, San Diego, USA

4. Division of Genetics and Cell Biology, and 4. Division of Neuroscience, San Raffaele Scientific Institute, DIBIT, 20132 Milan, Italy

Abstract

Correct myelination is crucial for the function of the peripheral nervous system. Both positive and negative regulators within the axon and Schwann cell function to ensure the correct onset and progression of myelination during both development and following peripheral nerve injury and repair. The Sox2 transcription factor is well known for its roles in the development and maintenance of progenitor and stem cell populations, but has also been proposed in vitro as a negative regulator of myelination in Schwann cells. We wished to test fully whether Sox2 regulates myelination in vivo and show here that sustained Sox2 expression in vivo blocks myelination in the peripheral nerves and maintains Schwann cells in a proliferative non-differentiated state, associated also with increased inflammation within the nerve. The plasticity of Schwann cells allows them to re-myelinate regenerated axons following injury and we show that re-myelination is also blocked by Sox2 expression in Schwann cells. These findings identify Sox2 as a physiological regulator of Schwann cell myelination in vivo and its potential to play a role in disorders of myelination in the peripheral nervous system.

Funder

Wellcome Trust

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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