FLRT Proteins Are Endogenous Latrophilin Ligands and Regulate Excitatory Synapse Development

FLRT Proteins Are Endogenous Latrophilin Ligands and Regulate Excitatory Synapse Development

Latrophilins (LPHNs) are a small family of G protein-coupled receptors known to mediate the massive synaptic exocytosis caused by the black widow spider venom α-latrotoxin, but their endogenous ligands and function remain unclear. Mutations in LPHN3 are strongly associated with attention deficit hyperactivity disorder, suggesting a role for latrophilins in human cognitive function. Using affini...

Supplemental Information Postsynaptic FLRT Proteins Are Endogenous Ligands for the Black Widow Spider Venom Receptor Latrophilin and Regulate Excitatory Synapse Development

Structural Basis of Latrophilin-FLRT Interaction

Latrophilins, receptors for spider venom α-latrotoxin, are adhesion type G-protein-coupled receptors with emerging functions in synapse development. The N-terminal region binds the endogenous cell adhesion molecule FLRT, a major regulator of cortical and synapse development. We present crystallographic data for the mouse Latrophilin3 lectin and olfactomedin-like (Olf) domains, thereby revealing...

Ephecting Excitatory Synapse Development

Alterations in synapse number and morphology are associated with devastating psychiatric and neurologic disorders. In this issue of Cell, Margolis et al. (2010) show that the RhoA-guanine exchange factor (GEF) Ephexin5 limits the numbers of excitatory synapses that neurons receive, thus identifying a new mechanism controlling synaptogenesis.

Structural Basis of Latrophilin-FLRT-UNC5 Interaction in Cell Adhesion.

Fibronectin leucine-rich repeat transmembrane proteins (FLRTs) are cell-adhesion molecules with emerging functions in cortical development and synapse formation. Their extracellular regions interact with latrophilins (LPHNs) to mediate synapse development, and with Uncoordinated-5 (UNC5)/netrin receptors to control the migration of neurons in the developing cortex. Here, we present the crystal ...