Guest guest Posted February 16, 2011 Report Share Posted February 16, 2011 Hi , Here's the Abstract. It is also most likely in our 2010 Archives. I can't remember if I had the full text or only the Abstract. If you can't find the full text, try contacting Dr. Suter at the Institute. Gretchen Science. 2010 Jun 11;328(5984):1415-8. Epub 2010 May 6. Dlg1-PTEN interaction regulates myelin thickness to prevent damaging peripheral nerve overmyelination. Cotter L, Ozçelik M, C, Pereira JA, Locher V, Baumann R, Relvas JB, Suter U, Tricaud N. Institute of Cell Biology, Department of Biology, Eidgenössische Technische Hochschule (ETH) Zürich, CH-8093 Zürich, Switzerland. Abstract The thickness of the myelin sheath that insulates axons is fitted for optimal nerve conduction velocity. Here, we show that, in Schwann cells, mammalian disks large homolog 1 (Dlg1) interacts with PTEN (phosphatase and tensin homolog deleted on chromosome 10) to inhibit axonal stimulation of myelination. This mechanism limits myelin sheath thickness and prevents overmyelination in mouse sciatic nerves. Removing this brake results also in myelin outfoldings and demyelination, characteristics of some peripheral neuropathies. Indeed, the Dlg1 brake is no longer functional in a mouse model of Charcot-Marie-Tooth disease. Therefore, negative regulation of myelination appears to be essential for optimization of nerve conduction velocity and myelin maintenance. Quote Link to comment Share on other sites More sharing options...
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