TY - JOUR
T1 - NRG1 type I dependent autoparacrine stimulation of Schwann cells in onion bulbs of peripheral neuropathies
AU - Fledrich, Robert
AU - Akkermann, Dagmar
AU - Schütza, Vlad
AU - Abdelaal, Tamer A.
AU - Hermes, Doris
AU - Schäffner, Erik
AU - Soto-Bernardini, M. Clara
AU - Götze, Tilmann
AU - Klink, Axel
AU - Kusch, Kathrin
AU - Krueger, Martin
AU - Kungl, Theresa
AU - Frydrychowicz, Clara
AU - Möbius, Wiebke
AU - Brück, Wolfgang
AU - Mueller, Wolf C.
AU - Bechmann, Ingo
AU - Sereda, Michael W.
AU - Schwab, Markus H.
AU - Nave, Klaus Armin
AU - Stassart, Ruth M.
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2019/12/1
Y1 - 2019/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85063748352&partnerID=8YFLogxK
U2 - 10.1038/s41467-019-09385-6
DO - 10.1038/s41467-019-09385-6
M3 - Artículo
C2 - 30931926
AN - SCOPUS:85063748352
SN - 2041-1723
VL - 10
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1467
ER -