Abstract
Glutamate delta-1 receptors (GluRδ1) are expressed in the adult hippocampus and inner ear and have recently been shown to be important for high-frequency hearing. Similar to the closest homolog glutamate delta-2 receptor (GluRδ2), no agonist-induced currents are observed from GluRδ1 receptors. In an effort to understand the function of the GluRδ1 subunit, we probed the conserved transmembrane 3 (TM3) region of the GluRδ1 subunit, where the GluRδ2 lurcher mutation is localized. Four mutations in the TM3 domain A650C, L652A, A654C, and F655A resulted in spontaneously open GluRδ1 channels suggesting that GluRδ1 receptors can form homomeric receptors. The leak currents were partially blocked by pentamidine but showed negligible inhibition by NASP. It has been demonstrated that extracellular Ca2+ binds and stabilizes the ligand binding domain (LBD) dimer interface leading to potentiation of currents through GluRδ2Lc channels. We found that extracellular Ca2+ potentiated the spontaneous currents through GluRδ1F655A suggesting that extracellular Ca2+ may interact with the conserved residues at GluRδ1 LBD dimer interface. A recent study suggested that d-serine and glycine bind to the GluRδ2 LBD and reduce spontaneous currents through the GluRδ2Lc channels. d-Serine and glycine produced only a modest reduction of spontaneous currents through GluRδ1F655A and had no effect on the spontaneous current through GluRδ1L652A. However, spontaneous currents in a chimeric GluRδ1-δ2Lc were robustly inhibited by d-serine. These results suggest that the activation gate is conserved in GluRδ1 receptors. Moreover, the conformational changes induced by d-serine and extracellular Ca2+ are conserved among GluRδ1 and GluRδ2 receptors.
| Original language | English |
|---|---|
| Pages (from-to) | 1-8 |
| Number of pages | 8 |
| Journal | Brain Research |
| Volume | 1382 |
| DOIs | |
| State | Published - Mar 25 2011 |
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All Science Journal Classification (ASJC) codes
- Neuroscience(all)
- Clinical Neurology
- Developmental Biology
- Molecular Biology
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Mutations in the transmembrane domain M3 generate spontaneously open orphan glutamate delta 1 receptor. / Yadav, Roopali; Rimerman, Ronald; Scofield, Margaret A.; Dravid, Shashank M.
In: Brain Research, Vol. 1382, 25.03.2011, p. 1-8.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Mutations in the transmembrane domain M3 generate spontaneously open orphan glutamate delta 1 receptor
AU - Yadav, Roopali
AU - Rimerman, Ronald
AU - Scofield, Margaret A.
AU - Dravid, Shashank M.
PY - 2011/3/25
Y1 - 2011/3/25
N2 - Glutamate delta-1 receptors (GluRδ1) are expressed in the adult hippocampus and inner ear and have recently been shown to be important for high-frequency hearing. Similar to the closest homolog glutamate delta-2 receptor (GluRδ2), no agonist-induced currents are observed from GluRδ1 receptors. In an effort to understand the function of the GluRδ1 subunit, we probed the conserved transmembrane 3 (TM3) region of the GluRδ1 subunit, where the GluRδ2 lurcher mutation is localized. Four mutations in the TM3 domain A650C, L652A, A654C, and F655A resulted in spontaneously open GluRδ1 channels suggesting that GluRδ1 receptors can form homomeric receptors. The leak currents were partially blocked by pentamidine but showed negligible inhibition by NASP. It has been demonstrated that extracellular Ca2+ binds and stabilizes the ligand binding domain (LBD) dimer interface leading to potentiation of currents through GluRδ2Lc channels. We found that extracellular Ca2+ potentiated the spontaneous currents through GluRδ1F655A suggesting that extracellular Ca2+ may interact with the conserved residues at GluRδ1 LBD dimer interface. A recent study suggested that d-serine and glycine bind to the GluRδ2 LBD and reduce spontaneous currents through the GluRδ2Lc channels. d-Serine and glycine produced only a modest reduction of spontaneous currents through GluRδ1F655A and had no effect on the spontaneous current through GluRδ1L652A. However, spontaneous currents in a chimeric GluRδ1-δ2Lc were robustly inhibited by d-serine. These results suggest that the activation gate is conserved in GluRδ1 receptors. Moreover, the conformational changes induced by d-serine and extracellular Ca2+ are conserved among GluRδ1 and GluRδ2 receptors.
AB - Glutamate delta-1 receptors (GluRδ1) are expressed in the adult hippocampus and inner ear and have recently been shown to be important for high-frequency hearing. Similar to the closest homolog glutamate delta-2 receptor (GluRδ2), no agonist-induced currents are observed from GluRδ1 receptors. In an effort to understand the function of the GluRδ1 subunit, we probed the conserved transmembrane 3 (TM3) region of the GluRδ1 subunit, where the GluRδ2 lurcher mutation is localized. Four mutations in the TM3 domain A650C, L652A, A654C, and F655A resulted in spontaneously open GluRδ1 channels suggesting that GluRδ1 receptors can form homomeric receptors. The leak currents were partially blocked by pentamidine but showed negligible inhibition by NASP. It has been demonstrated that extracellular Ca2+ binds and stabilizes the ligand binding domain (LBD) dimer interface leading to potentiation of currents through GluRδ2Lc channels. We found that extracellular Ca2+ potentiated the spontaneous currents through GluRδ1F655A suggesting that extracellular Ca2+ may interact with the conserved residues at GluRδ1 LBD dimer interface. A recent study suggested that d-serine and glycine bind to the GluRδ2 LBD and reduce spontaneous currents through the GluRδ2Lc channels. d-Serine and glycine produced only a modest reduction of spontaneous currents through GluRδ1F655A and had no effect on the spontaneous current through GluRδ1L652A. However, spontaneous currents in a chimeric GluRδ1-δ2Lc were robustly inhibited by d-serine. These results suggest that the activation gate is conserved in GluRδ1 receptors. Moreover, the conformational changes induced by d-serine and extracellular Ca2+ are conserved among GluRδ1 and GluRδ2 receptors.
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U2 - 10.1016/j.brainres.2010.12.086
DO - 10.1016/j.brainres.2010.12.086
M3 - Article
C2 - 21215726
AN - SCOPUS:79952535975
VL - 1382
SP - 1
EP - 8
JO - Brain Research
JF - Brain Research
SN - 0006-8993
ER -