Literature DB >> 28743796

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

Sheridan L Roberts1, Xin-Peng Dun1, Robin D S Doddrell1, Thomas Mindos1, Louisa K Drake2, Mark W Onaitis3, Francesca Florio4, Angelo Quattrini5, Alison C Lloyd6, Maurizio D'Antonio4, David B Parkinson7.   

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, in mice, sustained Sox2 expression in vivo blocks myelination in the peripheral nerves and maintains Schwann cells in a proliferative non-differentiated state, which is also associated 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.
© 2017. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Mouse; Myelination; Peripheral nervous system; Repair; Schwann cell; Sox2

Mesh:

Substances:

Year:  2017        PMID: 28743796      PMCID: PMC5611958          DOI: 10.1242/dev.150656

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  64 in total

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Journal:  Neuron       Date:  2000-05       Impact factor: 17.173

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3.  N-cadherin mediates axon-aligned process growth and cell-cell interaction in rat Schwann cells.

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4.  The Ras/Raf/ERK signalling pathway drives Schwann cell dedifferentiation.

Authors:  Marie C Harrisingh; Elena Perez-Nadales; David B Parkinson; Denise S Malcolm; Anne W Mudge; Alison C Lloyd
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5.  Functional consequences of mutations in the early growth response 2 gene (EGR2) correlate with severity of human myelinopathies.

Authors:  L E Warner; J Svaren; J Milbrandt; J R Lupski
Journal:  Hum Mol Genet       Date:  1999-07       Impact factor: 6.150

6.  EGR2 mutations in inherited neuropathies dominant-negatively inhibit myelin gene expression.

Authors:  R Nagarajan; J Svaren; N Le; T Araki; M Watson; J Milbrandt
Journal:  Neuron       Date:  2001-05       Impact factor: 17.173

7.  Analysis of congenital hypomyelinating Egr2Lo/Lo nerves identifies Sox2 as an inhibitor of Schwann cell differentiation and myelination.

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-02-03       Impact factor: 11.205

8.  Transforming growth factor beta (TGFbeta) mediates Schwann cell death in vitro and in vivo: examination of c-Jun activation, interactions with survival signals, and the relationship of TGFbeta-mediated death to Schwann cell differentiation.

Authors:  D B Parkinson; Z Dong; H Bunting; J Whitfield; C Meier; H Marie; R Mirsky; K R Jessen
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9.  Regulation of the myelin gene periaxin provides evidence for Krox-20-independent myelin-related signalling in Schwann cells.

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Journal:  J Cell Biol       Date:  2004-02-02       Impact factor: 10.539

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  29 in total

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7.  Evaluation of two methods to isolate Schwann cells from murine sciatic nerve.

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9.  Cell Shape and Matrix Stiffness Impact Schwann Cell Plasticity via YAP/TAZ and Rho GTPases.

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