Meeting details menu

Meeting Authors
Meeting Abstracts
Keynote lectures
Oral communications
Poster presentations
Special symposia
Other

Acta Physiologica Congress

Back

Acta Physiologica 2006; Volume 186, Supplement 650
Joint Meeting of The German Society of Physiology and The Federation of European Physiological Societies 2006
3/26/2006-3/29/2006
Ludwig-Maximilians-University, Munich


NG2-EXPRESSING CELLS IN GLIAL-AXON RECOGNITION AND MYELINATION.
Abstract number: ST4-4

Trotter1 J

1Molecular Cell Biology, Dept. of Biology, Johannes Gutenberg University of Mainz

NG2-expressing cells are a heterogeneous population of cells in the central and peripheral nervous systems. NG2 is expressed by oligodendrocyte and Schwann cell progenitors and down-regulated as these cells mature and express myelin proteins. In addition it is expressed by cells in grey matter in developing and adult brain that make close contact to neurons.

NG2 is a type I membrane protein with a PDZ-recognition domain at the intracellular C-terminus. PDZ-binding partners of NG2 include GRIP which binds also to GluRB and GluRC subunits of AMPA receptors expressed by immature glial cells. NG2, GRIP and AMPA receptors may thus form a tripartite complex at the contact site between the glial cell and glutamate releasing neurons. NG2 also binds Syntenin, which can interact with the cytoskeleton and may thus play a role in the motility of NG2-expressing cells and their processes.

NG2-expressing cells appear to play a role in the remyelination of demyelinated lesions. Some Multiple Sclerosis patients make antibodies against NG2 and these could conceivably influence the disease by inhibiting remyelination or adversely influencing glial-neuronal signalling at e.g. synapses.

Supported by the Deutsche Forschungsgemeinschaft and the gemeinnützige Hertie- Stiftung.

To cite this abstract, please use the following information:
Acta Physiologica 2006; Volume 186, Supplement 650 :ST4-4

Our site uses cookies to improve your experience.You can find out more about our use of cookies in our standard cookie policy, including instructions on how to reject and delete cookies if you wish to do so.

By continuing to browse this site you agree to us using cookies as described in our standard cookie policy .

CLOSE