4.6 Article

Sox10 Is Required for Schwann-Cell Homeostasis and Myelin Maintenance in the Adult Peripheral Nerve

Journal

GLIA
Volume 59, Issue 7, Pages 1022-1032

Publisher

WILEY-BLACKWELL
DOI: 10.1002/glia.21173

Keywords

Sry; high-mobility-group; glia; myelin; transcriptional control; conditional mouse mutagenesis; peripheral neuropathy; Charcot-Marie-Tooth disease

Categories

Funding

  1. IZKF Erlangen
  2. Deutsche Forschungsgemeinschaft [We1326/8-1, FOR 1075, TP5]
  3. Swiss National Science Foundation
  4. National Center of Competence in Research (NCCR)

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The transcription factor Sox10 functions during multiple consecutive stages of Schwann-cell development in the peripheral nervous system (PNS). Although Sox10 continues to be expressed in mature Schwann cells of the adult peripheral nerve, it is currently unclear whether it is still functional. Here, we used a genetic strategy to selectively delete Sox10 in glia of adult mice in a tamoxifen-dependent manner. The tamoxifen-treated mice developed a severe peripheral neuropathy that was associated with dramatic alterations in peripheral nerve structure and function. Demyelination and axonal degeneration were as much evident as signs of neuroinflammation. Compound action potentials exhibited pathophysiological alterations. Sox10-deleted Schwann cells persisted in the peripheral nerve, but did not exhibit a mature, myelinating phenotype arguing that Sox10 is rather required for differentiation and maintenance of the differentiated state than for survival. Our report is the first evidence that Sox10 is still essentially required for Schwann-cell function in the adult PNS and establishes a useful model in which to study human peripheral neuropathies. (C) 2011 Wiley-Liss, Inc.

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