The Nogo Receptor Ligand LGI1 Regulates Synapse Number and Synaptic Activity in Hippocampal and Cortical Neurons

ENeuro
Rhalena ThomasPhilip A Barker

Abstract

Leucine-rich glioma-inactivated protein 1 (LGI1) is a secreted neuronal protein and a Nogo receptor 1 (NgR1) ligand. Mutations in LGI1 in humans causes autosomal dominant lateral temporal lobe epilepsy and homozygous deletion of LGI1 in mice results in severe epileptic seizures that cause early postnatal death. NgR1 plays an important role in the development of CNS synapses and circuitry by limiting plasticity in the adult cortex via the activation of RhoA. These relationships and functions prompted us to examine the effect of LGI1 on synapse formation in vitro and in vivo. We report that application of LGI1 increases synaptic density in neuronal culture and that LGI1 null hippocampus has fewer dendritic mushroom spines than in wild-type (WT) littermates. Further, our electrophysiological investigations demonstrate that LGI1 null hippocampal neurons possess fewer and weaker synapses. RhoA activity is significantly increased in cortical cultures derived from LGI1 null mice and using a reconstituted system; we show directly that LGI1 antagonizes NgR1-tumor necrosis factor receptor orphan Y (TROY) signaling. Our data suggests that LGI1 enhances synapse formation in cortical and hippocampal neurons by reducing NgR1 signaling.

Citations

May 7, 2021·Small GTPases·Joseph G DumanKimberley F Tolias
Aug 18, 2021·Neurobiology of Stress·Seung Hoon LeeHyeon Son
Dec 31, 2021·Cellular and Molecular Life Sciences : CMLS·Paul BaudinVincent Navarro

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Methods Mentioned

BETA
pulldown
GTPase

Software Mentioned

NIH ImageJ
GraphPad
Zen
Fiji
ImageJ
GraphPad Prism
ImageJ Analyze Particles

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