Article
A mouse model of Schwartz-Jampel syndrome reveals myelinating Schwann cell dysfunction with persistent axonal depolarization in vitro and distal peripheral nerve hyperexcitability when perlecan is lacking.
The American journal of pathology - 1 May 2012
Bangratz Marie, Sarrazin Nadège, Devaux Jérôme, Zambroni Désirée, Echaniz-Laguna Andoni, René Frédérique, Boërio Delphine, Davoine Claire-Sophie, Fontaine Bertrand, Feltri Maria Laura, Benoit Evelyne, Nicole Sophie
Abstract excerpt
Congenital peripheral nerve hyperexcitability (PNH) is usually associated with impaired function of voltage-gated K(+) channels (VGKCs) in neuromyotonia and demyelination in peripheral neuropathies. Schwartz-Jampel syndrome (SJS) is a form of PNH that is due to hypomorphic mutations of perlecan, the major proteoglycan of basement membranes. Schwann cell basement membrane and its cell receptors are critical for...
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