
mGlu receptors in the retina
Author(s) -
Dhingra Anuradha,
Vardi Noga
Publication year - 2012
Publication title -
wiley interdisciplinary reviews: membrane transport and signaling
Language(s) - English
Resource type - Journals
eISSN - 2190-4618
pISSN - 2190-460X
DOI - 10.1002/wmts.43
Subject(s) - metabotropic glutamate receptor 6 , metabotropic glutamate receptor , neuroscience , biology , class c gpcr , metabotropic glutamate receptor 7 , amacrine cell , metabotropic glutamate receptor 1 , retina , metabotropic glutamate receptor 2 , neurotransmission , microbiology and biotechnology , metabotropic glutamate receptor 8 , glutamate receptor , receptor , biochemistry
Glutamate, a key neurotransmitter in the vertebrate retina, acts via ionotropic and metabotropic receptors. Retina expresses mRNA for all metabotropic glutamate receptors and proteins for all but mGluR3. Every retinal cell class expresses one or more of these receptors. In general, these receptors are present presynaptically and serve to modulate synaptic transmission. While mGluRs on the photoreceptor terminal act as autoreceptors to titer glutamate levels, those on the horizontal cell processes seem to shape the light response. Similarly, autoreceptors on bipolar axon terminals modulate glutamate release and the receptors on amacrine and ganglion cells modulate feedforward signals by modulating K + or Ca 2+ current to fine tune light responses. Since most of the mGluR subtypes are present in amacrine and ganglion cells that belong to many cell types, the pathways downstream of mGluRs are highly diverse with primarily modulatory effects. An exception to most mGluRs that have a modulatory function is mGluR6 because it plays a key role in the feedforward transmission from photoreceptors to ON bipolar cells and is also required for the correct localization of the synaptic proteins in the dendritic tips. In humans, mutations in the gene encoding mGluR6 cause autosomal recessive night blindness. In addition, mGluRs appear to play a trophic role in development and after retinal damage, suggesting potential future therapeutic implications. WIREs Membr Transp Signal 2012, 1:641–653. doi: 10.1002/wmts.43 For further resources related to this article, please visit the WIREs website .