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A dual role of erbB2 in myelination and in expansion of the Schwann cell precursor pool

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Official URL:http://www.jcb.org/cgi/content/abstract/148/5/1035
PubMed:View item in PubMed
Creators Name:Garratt, A.N. and Voiculescu, O. and Topilko, P. and Charnay, P. and Birchmeier, C.
Journal Title:Journal of Cell Biology
Journal Abbreviation:J Cell Biol
Volume:148
Number:5
Page Range:1035-1046
Date:6 March 2000
Keywords:Cre-loxP, Neuregulin, Myelin, Glia, Neuropathy , Animals, Mice
Abstract:Neuregulin-1 provides an important axonally derived signal for the survival and growth of developing Schwann cells, which is transmitted by the ErbB2/ErbB3 receptor tyrosine kinases. Null mutations of the neuregulin-1, erbB2, or erbB3 mouse genes cause severe deficits in early Schwann cell development. Here, we employ Cre-loxP technology to introduce erbB2 mutations late in Schwann cell development, using a Krox20-cre allele. Cre-mediated erbB2 ablation occurs perinatally in peripheral nerves, but already at E11 within spinal roots. The mutant mice exhibit a widespread peripheral neuropathy characterized by abnormally thin myelin sheaths, containing fewer myelin wraps. In addition, in spinal roots the Schwann cell precursor pool is not correctly established. Thus, the Neuregulin signaling system functions during multiple stages of Schwann cell development and is essential for correct myelination. The thickness of the myelin sheath is determined by the axon diameter, and we suggest that trophic signals provided by the nerve determine the number of times a Schwann cell wraps an axon.
ISSN:0021-9525
Publisher:Rockefeller University Press (U.S.A.)
Additional Information:Copyright (c) 2000 by The Rockefeller University Press
Item Type:Article

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