Orphan glutamate receptor δ1 subunit required for high-frequency hearing

Jiangang Gao, Stephane F. Maison, Xudong Wu, Keiko Hirose, Sherri M. Jones, Ildar Bayazitov, Yong Tian, Guy Mittleman, Douglas B. Matthews, Stanislav S. Zakharenko, M. Charles Liberman, Jian Zuo

Research output: Contribution to journalArticlepeer-review

47 Scopus citations


The function of the orphan glutamate receptor delta subunits (GluRδ1 and GluRδ2) remains unclear. GluRδ2 is expressed exclusively in the Purkinje cells of the cerebellum, and GluRδ1 is prominently expressed in inner ear hair cells and neurons of the hippocampus. We found that mice lacking the GluRδ1 protein displayed significant cochlear threshold shifts for frequencies of >16 kHz. These deficits correlated with a substantial loss of type IV spiral ligament fibrocytes and a significant reduction of endolymphatic potential in high-frequency cochlear regions. Vulnerability to acoustic injury was significantly enhanced; however, the efferent innervation of hair cells and the classic efferent inhibition of outer hair cells were unaffected. Hippocampal and vestibular morphology and function were normal. Our findings show that the orphan GluRδ1 plays an essential role in high-frequency hearing and ionic homeostasis in the basal cochlea, and the locus encoding GluRδ1 represents a candidate gene for congenital or acquired high-frequency hearing loss in humans.

Original languageEnglish
Pages (from-to)4500-4512
Number of pages13
JournalMolecular and cellular biology
Issue number12
StatePublished - Jun 2007


Dive into the research topics of 'Orphan glutamate receptor δ1 subunit required for high-frequency hearing'. Together they form a unique fingerprint.

Cite this