Journal article
SynCAM, a synaptic adhesion molecule that drives synapse assembly
Science (American Association for the Advancement of Science), Vol.297(5586), pp.1525-1531
08/30/2002
DOI: 10.1126/science.1072356
PMID: 12202822
Abstract
Synapses, the junctions between nerve cells through which they communicate, are formed by the coordinated assembly and tight attachment of pre- and postsynaptic specializations. We now show that SynCAM is a brain-specific, immunoglobulin domain-containing protein that binds to intracellular PDZ-domain proteins and functions as a homophilic cell adhesion molecule at the synapse. Expression of the isolated cytoplasmic tail of SynCAM in neurons inhibited synapse assembly. Conversely, expression of full-length SynCAM in nonneuronal cells induced synapse formation by cocultured hippocampal neurons with normal release properties. Glutamatergic synaptic transmission was reconstituted in these nonneuronal cells by coexpressing glutamate receptors with SynCAM, which suggests that a single type of adhesion molecule and glutamate receptor are sufficient for a functional postsynaptic response.
Details
- Title: Subtitle
- SynCAM, a synaptic adhesion molecule that drives synapse assembly
- Creators
- Thomas Biederer - Center for Basic Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. Thomas.Biederer@UTSouthwestern.eduYildirim SaraMarina MozhayevaDeniz AtasoyXinran LiuEge T KavalaliThomas C Südhof
- Resource Type
- Journal article
- Publication Details
- Science (American Association for the Advancement of Science), Vol.297(5586), pp.1525-1531
- Publisher
- United States
- DOI
- 10.1126/science.1072356
- PMID
- 12202822
- ISSN
- 0036-8075
- eISSN
- 1095-9203
- Language
- English
- Date published
- 08/30/2002
- Academic Unit
- Iowa Neuroscience Institute; Fraternal Order of Eagles Diabetes Research Center; Neuroscience and Pharmacology
- Record Identifier
- 9984040351902771
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