TY - JOUR
T1 - A GluD Coming-Of-Age Story
AU - Yuzaki, Michisuke
AU - Aricescu, A. Radu
N1 - Funding Information:
This work was funded by the UK Medical Research Council (MRC) (grant L009609 to A.R.A.), the Japan Society for the Promotion of Science (grant 15H05772 to M.Y.) and the Human Frontier Science Program (grant RGP0065/2014 to M.Y. and A.R.A.).
Publisher Copyright:
© 2016 Elsevier Ltd
PY - 2017/3/1
Y1 - 2017/3/1
N2 - The GluD1 and GluD2 receptors form the GluD ionotropic glutamate receptor (iGluR) subfamily. Without known endogenous ligands, they have long been referred to as ‘orphan’ and remained enigmatic functionally. Recent progress has, however, radically changed this view. Both GluD receptors are expressed in wider brain regions than originally thought. Human genetic studies and analyses of knockout mice have revealed their involvement in multiple neurodevelopmental and psychiatric disorders. The discovery of endogenous ligands, together with structural investigations, has opened the way towards a mechanistic understanding of GluD signaling at central nervous system synapses. These studies have also prompted the hypothesis that all iGluRs, and potentially other neurotransmitter receptors, rely on the cooperative binding of extracellular small-molecule and protein ligands for physiological signaling.
AB - The GluD1 and GluD2 receptors form the GluD ionotropic glutamate receptor (iGluR) subfamily. Without known endogenous ligands, they have long been referred to as ‘orphan’ and remained enigmatic functionally. Recent progress has, however, radically changed this view. Both GluD receptors are expressed in wider brain regions than originally thought. Human genetic studies and analyses of knockout mice have revealed their involvement in multiple neurodevelopmental and psychiatric disorders. The discovery of endogenous ligands, together with structural investigations, has opened the way towards a mechanistic understanding of GluD signaling at central nervous system synapses. These studies have also prompted the hypothesis that all iGluRs, and potentially other neurotransmitter receptors, rely on the cooperative binding of extracellular small-molecule and protein ligands for physiological signaling.
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U2 - 10.1016/j.tins.2016.12.004
DO - 10.1016/j.tins.2016.12.004
M3 - Review article
C2 - 28110935
AN - SCOPUS:85009804153
SN - 0166-2236
VL - 40
SP - 138
EP - 150
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - 3
ER -