The cellular and molecular landscape of neuroligins

被引:127
作者
Bemben, Michael A. [1 ,2 ]
Shipman, Seth L. [3 ,4 ]
Nicoll, Roger A. [5 ,6 ]
Roche, Katherine W. [1 ]
机构
[1] NINDS, Receptor Biol Sect, NIH, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Harvard Univ, Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[5] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[6] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94158 USA
关键词
SYNAPTIC-TRANSMISSION; INHIBITORY SYNAPSES; ADHESION MOLECULES; NEUREXIN COMPLEX; AUTISM; PROTEIN; MUTATION; BINDING; HIPPOCAMPAL; DOMAIN;
D O I
10.1016/j.tins.2015.06.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A fundamental physical interaction exists across the synapse. It is mediated by synaptic adhesion molecules, and is among the earliest and most indispensable of molecular events occurring during synaptogenesis. The regulation of adhesion molecules and their interactions with other synaptic proteins likely affect not only on synapse formation but also on ongoing synaptic function. We review research on one major family of postsynaptic adhesion molecules, neuroligins, which bind to their presynaptic partner neurexin across the synaptic cleft. We move from a structural overview to the broad cellular and synaptic context of neuroligins, intermolecular interactions, and molecular modifications that occur within a synapse. Finally, we examine evidence concerning the physiological functions of neuroligin in a cell and highlight areas requiring further investigation.
引用
收藏
页码:496 / 505
页数:10
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