Condensates of synaptic vesicles and synapsin-1 mediate actin sequestering and polymerization

Neuronal communication relies on precisely maintained synaptic vesicle (SV) clusters, which assemble via liquid-liquid phase separation. This process requires synapsins, the major synaptic phosphoproteins, which are known to bind actin. Reorganization of SVs, synapsins, and actin is a hallmark of synaptic activity, but the molecular details of the interactions between these components remain unclear. Here, we combine in vitro reconstitution with expansion microscopy, super-resolution imaging, and cryo-electron tomography to dissect the roles of SV-synapsin-1 condensates in the organization of the presynaptic actin cytoskeleton. Our results indicate that condensation of synapsin-1 initiates actin polymerization. This process enables SV-synapsin-actin assemblies to facilitate the mesoscale organization of SV clusters along axons, which is similar to the native presynaptic organization observed at both lamprey and mammalian synapses. Understanding the relationship between the actin network and synapsin-synaptic vesicle condensates can help elucidate how coordinated neurotransmission along the axon enables circuit function and behavior.

Authors

Institutions

Publication Details

Journal
The EMBO Journal
Published
2025-08-14
DOI
https://doi.org/10.1038/s44318-025-00516-y
Citations
4
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
3.22
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Condensates of synaptic vesicles and synapsin-1 mediate actin sequestering and polymerization

Cristina Román‐Vendrell, Arsen Petrović, Dragomir Milovanović, Jaqulin N. Wallace et al.
4 citations
The EMBO Journal
RNA Research and Splicing
3.22
article

Condensates of synaptic vesicles and synapsin-1 mediate actin sequestering and polymerization

Cristina Román‐Vendrell, Arsen Petrović, Dragomir Milovanović, Jaqulin N. Wallace, Branislava Ranković, Александр Коробейников, Jakob Rentsch, Christian Hoffmann, Jennifer R. Morgan, Johannes Vincent Tromm, Sarah Köster, Tommaso Volpi, Rubén Fernández‐Busnadiego, Silvio O. Rizzoli, Linda Kokwaro, Akshita Chhabra, Nadja Hümpfer, Helge Ewers, Eleonora Perego, Emma Johnson, Gerard Aguilar Pérez, Luka Gnidovec
article en
4 citations

Abstract

Neuronal communication relies on precisely maintained synaptic vesicle (SV) clusters, which assemble via liquid-liquid phase separation. This process requires synapsins, the major synaptic phosphoproteins, which are known to bind actin. Reorganization of SVs, synapsins, and actin is a hallmark of synaptic activity, but the molecular details of the interactions between these components remain unclear. Here, we combine in vitro reconstitution with expansion microscopy, super-resolution imaging, and cryo-electron tomography to dissect the roles of SV-synapsin-1 condensates in the organization of the presynaptic actin cytoskeleton. Our results indicate that condensation of synapsin-1 initiates actin polymerization. This process enables SV-synapsin-actin assemblies to facilitate the mesoscale organization of SV clusters along axons, which is similar to the native presynaptic organization observed at both lamprey and mammalian synapses. Understanding the relationship between the actin network and synapsin-synaptic vesicle condensates can help elucidate how coordinated neurotransmission along the axon enables circuit function and behavior.

The EMBO JournalVol. 44(18)
Marine Biological Laboratory (US), German Center for Neurodegenerative Diseases (DE), Yale University (US), Humboldt-Universität zu Berlin (DE), Universitätsmedizin Göttingen (DE), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), University of Göttingen (DE), Freie Universität Berlin (DE)
Openalex Percentile: Top 8%
RNA Research and Splicing
3.22
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.