The δ2 glutamate receptor

10 Years later

Research output: Contribution to journalArticle

89 Citations (Scopus)

Abstract

The orphan glutamate receptor δ2 (GluRδ2) is predominantly expressed in Purkinje cells and plays a crucial role in cerebellar functions: mice that lack the GluRδ2 gene display ataxia and impaired synaptic plasticity. However, when expressed alone or with other glutamate receptors, GluRδ2 does not form functional glutamate-gated ion channels nor does it bind to glutamate analogs. Therefore, the mechanisms by which GluRδ2 participates in cerebellar functions have been elusive. Studies of mutant mice such as lurcher, hotfoot, and GluRδ2 knockout mice have provided clues to the structure and function of GluRδ2. GluRδ2 has a channel pore similar to that of other glutamate receptors; the channel is functional at least when the lurcher mutation is present. GluRδ2 must be transported to the Purkinje cell surface to function; the absence of surface GluRδ2 causes the ataxic phenotype of hotfoot mice. In GluRδ2-null mice, the presence of naked spines not innervated by parallel fibers may influence the sustained innervation of mutant Purkinje cells by multiple climbing fibers. From these results, several hypotheses about mechanisms by which GluRδ2 functions are proposed in this article. Further characterization of GluRδ2's functions will provide key insights into normal and abnormal cerebellar functions.

Original languageEnglish
Pages (from-to)11-22
Number of pages12
JournalNeuroscience Research
Volume46
Issue number1
DOIs
Publication statusPublished - 2003 May 1
Externally publishedYes

Fingerprint

Glutamate Receptors
Purkinje Cells
Glutamic Acid
Neuronal Plasticity
Ataxia
Ion Channels
Knockout Mice
Spine

Keywords

  • Ataxia
  • Cerebellum
  • Grid2
  • Mutant
  • Orphan
  • Plasticity
  • Purkinje cells

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

The δ2 glutamate receptor : 10 Years later. / Yuzaki, Michisuke.

In: Neuroscience Research, Vol. 46, No. 1, 01.05.2003, p. 11-22.

Research output: Contribution to journalArticle

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