ReviewJournal of neurochemistry2025
Synaptic Vesicle Recycling at the Developing Presynapse.
Review in Journal of neurochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed.
- Syntaxin1A in synaptopathies: From molecular mechanisms to therapeutic implications in neurological disorders (Review).Biomedical reports · 2026Review
- Molecular Physiology of the Neuronal Synapse.Current issues in molecular biology · 2026Review
- Benchmarking In-Cell Proteomics for Profiling Neuroblastoma Cell Differentiation and the Ubiquitin-Proteasome System.Journal of proteome research · 2025Article
- Synaptic Vesicle Recycling at the Developing Presynapse.Journal of neurochemistry · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Neurotransmitter release plays a fundamental role in brain communication. This is mediated via the exocytosis of neurotransmitter-containing synaptic vesicles (SVs) at the presynapse. After fusion with the presynaptic plasma membrane, SVs are regenerated by endocytosis and recycled back into functional pools. The great majority of research that has studied this essential process has focused on SV recycling at the mature presynaptic terminal. In contrast, SV recycling in immature neurons remains poorly understood, even though its disruption is heavily associated with a series of neurodevelopmental disorders. Evidence is accumulating that developing neurons display distinct presynaptic mechanisms for SV recycling. For example, developing presynapses display loose coupling between evoked calcium influx and SV fusion, with spontaneous SV exocytosis and clathrin-mediated endocytosis being the dominant exocytosis and endocytosis mechanisms respectively. In contrast, SV fusion in mature nerve terminals is tightly coupled to evoked calcium influx, with evoked SV exocytosis and endosomal modes of endocytosis dominant. This article reviews research at each stage of the SV recycling process at both mature and immature nerve terminals, beginning with the coupling of activity-dependent calcium influx to neurotransmitter release. In doing so, it aims to provide an integrated perspective of current knowledge regarding SV recycling through development across different neuronal systems, while posing key future questions to address for the presynaptic development field.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.