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PMID: 16337696 Published · ppublish English Journal Article Review

Neuroligins and neurexins: linking cell adhesion, synapse formation and cognitive function.

Trends in neurosciences ·Vol. 29 ·No. 1 ·2006-01-00 ·Pages 21-9

Dean C, Dresbach T

Abstract

Cell adhesion represents the most direct way of coordinating synaptic connectivity in the brain. Recent evidence highlights the importance of a trans-synaptic interaction between postsynaptic neuroligins and presynaptic neurexins. These transmembrane molecules bind each other extracellularly to promote adhesion between dendrites and axons. This signals the recruitment of presynaptic and postsynaptic molecules to form a functional synapse. Remarkably, neuroligins alone can induce the formation of fully functional presynaptic terminals in contacting axons. Conversely, neurexins alone can induce postsynaptic differentiation and clustering of receptors in dendrites. Therefore, the neuroligin-neurexin interaction has the unique ability to act as a bi-directional trigger of synapse formation. Here, we review several recent studies that offer clues as to how these proteins form synapses and how they might function in the brain to establish and modify neuronal network properties and cognition.

MeSH Terms
Activated-Leukocyte Cell Adhesion Molecule/metabolism Animals Brain/physiology Cell Adhesion/physiology Cell Adhesion Molecules/metabolism Cognition/physiology Humans Models, Neurological Nerve Tissue Proteins/metabolism Neurons/physiology Synapses/physiology Synaptic Transmission/physiology
Chemicals
Activated-Leukocyte Cell Adhesion Molecule Cell Adhesion Molecules Nerve Tissue Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Dean Camin
Department of Physiology, University of Wisconsin Medical School, Madison, WI 53706, USA. [email protected]
Dresbach Thomas
Article Info
Journal
Trends in neurosciences
Abbr.
Trends Neurosci
ISSN
0166-2236
Published
2006-01-00
Epub
2005-00-07
Pages
21-9
Language
English
Region
England
NLM ID
7808616
Subset
IM
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