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Glycine and glycine receptor signalling in non-neuronal cells

1
Institute of Biomedical Research, Hasselt University and transnationale Universiteit Limburg, Diepenbeek, Belgium
2
Kennedy Institute of Rheumatology Division, Faculty of Medicine, Imperial College London, Charing Cross Campus, London, UK
3
Department of Pharmacology, School of Pharmacy, University of London, London, UK
Glycine is an inhibitory neurotransmitter acting mainly in the caudal part of the central nervous system. Besides this neurotransmitter function, glycine has cytoprotective and modulatory effects in different non-neuronal cell types. Modulatory effects were mainly described in immune cells, endothelial cells and macroglial cells, where glycine modulates proliferation, differentiation, migration and cytokine production. Activation of glycine receptors (GlyRs) causes membrane potential changes that in turn modulate calcium flux and downstream effects in these cells. Cytoprotective effects were mainly described in renal cells, hepatocytes and endothelial cells, where glycine protects cells from ischemic cell death. In these cell types, glycine has been suggested to stabilize porous defects that develop in the plasma membranes of ischemic cells, leading to leakage of macromolecules and subsequent cell death. Although there is some evidence linking these effects to the activation of GlyRs, they seem to operate in an entirely different mode from classical neuronal subtypes.
Keywords:
glycine receptor, cytoprotection, glia, immune cells, renal cells, hepatocytes, endothelial cells
Citation:
Van den Eynden J, SahebAli S, Horwood N, Carmans S, Brône B, Hellings N, Steels P, Harvey RJ and Rigo J-M (2009). Glycine and glycine receptor signalling in non-neuronal cells. Front. Mol. Neurosci. 2:9. doi: 10.3389/neuro.02.009.2009
Received:
24 June 2009;
 Paper pending published:
13 July 2009;
Accepted:
23 July 2009;
 Published online:
20 August 2009.

Edited by:

Jochen C. Meier, Max Delbrück Center for Molecular Medicine, Germany

Reviewed by:

Luis Aguayo, Universidad de Concepción, Chile
Claudia Eder, University of London, UK
Copyright:
© 2009 Van den Eynden, SahebAli, Horwood, Carmans, Brône, Hellings, Steels, Harvey and Rigo. This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
*Correspondence:
Jean-Michel Rigo, Institute of Biomedical Research, Hasselt University and transnationale Universiteit Limburg, Agoralaan, Building C, B-3590 Diepenbeek, Belgium. e-mail: jeanmichel.rigo@uhasselt.be

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