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bioRxiv · 10.1101/077933

Interaction between distinct pools controls activity-dependent actin dynamics in the dendritic spine

Oleg O. Glebov·Juan Burrone
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Abstract

Actin cytoskeleton is composed of functionally distinct pools of filamentous (F)-actin defined by their regulatory machinery and dynamics. Although these networks may compete for actin monomers and regulatory factors1-4, the interaction between them remains poorly understood. Here, we show that disruption of the labile F-actin pool in neurons by limited actin depolymerization5,6 unexpectedly triggers rapid enhancement of the F-actin content at the dendritic spine. Long-term blockade of NMDA-type receptors decreases spine actin polymerization, which is specifically restored by the labile pool ablation. Increase in the spine actin is triggered by blockade of formin-induced actin polymerization in a manner dependent on Arp2/3 complex activity. Finally, limited actin depolymerization increases F-actin levels in a cultured cell line, suggesting the generality of the two-tiered actin dynamics. Based on these findings, we propose a model whereby the labile pool of F-actin controlled by formin restricts the polymerization state of the Arp2/3-regulated stable spine actin, suggesting a feedback principle at the core of cytoskeletal organization in neurons.\n\nHighlightsO_LIDisruption of labile F-actin by limited depolymerization rapidly increases the synaptic F-actin content;\nC_LIO_LIThe depolymerization-induced F-actin boost reverses decrease in synaptic F-actin induced by long-term NMDA receptor blockade;\nC_LIO_LIBlockade of formin-dependent actin polymerization boosts synaptic F-actin in an Arp2/3-dependent manner;\nC_LIO_LILimited actin depolymerization enhances overall F-actin content in a mammalian cell line.\nC_LI

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Oleg O. Glebov, Juan Burrone. 2016-09-27. Interaction between distinct pools controls activity-dependent actin dynamics in the dendritic spine. https://doi.org/10.1101/077933

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