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NRG1 type I dependent autoparacrine stimulation of Schwann cells in onion bulbs of peripheral neuropathies

  • Robert Fledrich
  • , Dagmar Akkermann
  • , Vlad Schütza
  • , Tamer A. Abdelaal
  • , Doris Hermes
  • , Erik Schäffner
  • , M. Clara Soto-Bernardini
  • , Tilmann Götze
  • , Axel Klink
  • , Kathrin Kusch
  • , Martin Krueger
  • , Theresa Kungl
  • , Clara Frydrychowicz
  • , Wiebke Möbius
  • , Wolfgang Brück
  • , Wolf C. Mueller
  • , Ingo Bechmann
  • , Michael W. Sereda
  • , Markus H. Schwab
  • , Klaus Armin Nave
  • Ruth M. Stassart

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

In contrast to acute peripheral nerve injury, the molecular response of Schwann cells in chronic neuropathies remains poorly understood. Onion bulb structures are a pathological hallmark of demyelinating neuropathies, but the nature of these formations is unknown. Here, we show that Schwann cells induce the expression of Neuregulin-1 type I (NRG1-I), a paracrine growth factor, in various chronic demyelinating diseases. Genetic disruption of Schwann cell-derived NRG1 signalling in a mouse model of Charcot-Marie-Tooth Disease 1A (CMT1A), suppresses hypermyelination and the formation of onion bulbs. Transgenic overexpression of NRG1-I in Schwann cells on a wildtype background is sufficient to mediate an interaction between Schwann cells via an ErbB2 receptor-MEK/ERK signaling axis, which causes onion bulb formations and results in a peripheral neuropathy reminiscent of CMT1A. We suggest that diseased Schwann cells mount a regeneration program that is beneficial in acute nerve injury, but that overstimulation of Schwann cells in chronic neuropathies is detrimental.

Original languageEnglish
Article number1467
JournalNature Communications
Volume10
Issue number1
DOIs
StatePublished - 1 Dec 2019

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