Cbln1 Is a Ligand for an Orphan Glutamate Receptor δ2, a Bidirectional Synapse Organizer

Author:

Matsuda Keiko1,Miura Eriko1,Miyazaki Taisuke2,Kakegawa Wataru1,Emi Kyoichi1,Narumi Sakae1,Fukazawa Yugo3,Ito-Ishida Aya14,Kondo Tetsuro15,Shigemoto Ryuichi3,Watanabe Masahiko2,Yuzaki Michisuke1

Affiliation:

1. Department of Physiology, School of Medicine, Keio University, Tokyo 160-8582, Japan.

2. Department of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan.

3. Division of Cerebral Structures, National Institutes for Physiological Sciences, Okazaki 444-8787, Japan.

4. Department of Cellular Neurobiology, Graduate School of Medicine, University of Tokyo, Tokyo 113-0033, Japan.

5. Molecular Neurophysiology, Neuroscience Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8566, Japan.

Abstract

Orphan No More The glutamate receptor δ2 (GluD2), another member of the ionotropic glutamate receptor family, has long been considered to be an orphan receptor because there are no known endogenous ligands. Nevertheless, GluD2 is essential for the normal development of cerebellar circuits. Using immunocytochemistry, binding assays, electrophysiology, and freeze-fracture electron microscopy, Matsuda et al. (p. 363 ) found that Cbln1, a soluble protein secreted from cerebellar granule cells, binds to the extracellular N terminus of GluD2 on Purkinje cells. Binding has two independent consequences: First, it leads to presynaptic differentiation and second, it causes postsynaptic clustering of several important synapse-specific molecules. Both events are needed for synapse formation between granule cells and Purkinje cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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