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NRG1 type I dependent autoparacrine stimulation of Schwann cells in onion bulbs of peripheral neuropathies
Date Issued
2019
Author(s)
Akkermann, Dagmar
Schütza, Vlad
Abdelaal, Tamer A.
Hermes, Doris
Schäffner, Erik
Soto-Bernardini, M. Clara
Götze, Tilmann
Klink, Axel
Krueger, Martin
Kungl, Theresa
Frydrychowicz, Clara
Mueller, Wolf C.
Bechmann, Ingo
Schwab, Markus H.
Stassart, Ruth M.
DOI
10.1038/s41467-019-09385-6
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.
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s41467-019-09385-6.pdf
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