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bioRxiv · 10.1101/2021.03.05.433425

Semaphorin3F Drives Dendritic Spine Pruning through Rho-GTPase Signaling

Duncan, B. W.·Mohan, V.·Wade, S. D.·Truong, Y.·Kampov-Polevoi, A.·Temple, B. R.·Maness, P. F.
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Abstract

Dendritic spines of cortical pyramidal neurons are initially overproduced then remodeled substantially in the adolescent brain to achieve appropriate excitatory balance in mature circuits. Here we investigated the molecular mechanism of developmental spine pruning by Semaphorin 3F (Sema3F) and its holoreceptor complex, which consists of immunoglobulin-class adhesion molecule NrCAM, Neuropilin-2 (Npn2), and PlexinA3 (PlexA3) signaling subunits. Structure-function studies of the NrCAM-Npn2 interface showed that NrCAM stabilizes binding between Npn2 and PlexA3 necessary for Sema3F-induced spine pruning. Using a mouse neuronal culture system, we identified a dual signaling pathway for Sema3F-induced pruning, which involves activation of Tiam1-Rac1-PAK1-3 -LIMK1/2-Cofilin1 and RhoA-ROCK1/2-Myosin II in dendritic spines. Inhibitors of actin remodeling impaired spine collapse in the cortical neurons. Elucidation of these pathways expands our understanding of critical events that sculpt neuronal networks and may provide insight into how interruptions to these pathways could lead to spine dysgenesis in diseases such as autism, bipolar disorder, and schizophrenia.

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Duncan, B. W., Mohan, V., Wade, S. D., Truong, Y., Kampov-Polevoi, A., Temple, B. R., Maness, P. F.. 2021-03-05. Semaphorin3F Drives Dendritic Spine Pruning through Rho-GTPase Signaling. https://doi.org/10.1101/2021.03.05.433425

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