Revisiting the Role of Clathrin-Mediated Endoytosis in Synaptic Vesicle Recycling
Open accessAbstract
Without robust mechanisms to efficiently form new synaptic vesicles (SVs), the tens to hundreds of SVs typically present at the neuronal synapse would be rapidly used up, even at modest levels of neuronal activity. SV recycling is thus critical for synaptic physiology and proper function of sensory and nervous systems. Yet, more than four decades after it was originally proposed that the SVs are formed and recycled locally at the presynaptic terminals, the mechanisms of endocytic processes at the synapse are heavily debated. Clathrin-mediated endocytosis, a type of endocytosis that capitalizes on the clathrin coat, a number of adaptor and accessory proteins, and the GTPase dynamin, is well understood, while the contributions of clathrin-independent fast endocytosis, kiss-and-run, bulk endocytosis and ultrafast endocytosis are still being evaluated. This review article revisits and summarizes the current knowledge on the SV reformation with a focus on clathrin-mediated endocytosis, and it discusses the modes of SV formation from endosome-like structures at the synapse. Given the importance of this topic, future advances in this active field are expected to contribute to better comprehension of neurotransmission, and to have general implications for neuroscience and medicine.
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Ultrafast bulk endocytosis and activity-dependent bulk endocytosis are also responsible for recycling of vesicles.
“Apart from those mechanisms, several other mechanisms, such as ultrafast bulk endocytosis and activity-dependent bulk endocytosis, are also responsible for the recycling of the vesicles [150,151].”
From Insights of Endocytosis Signaling in Health and Disease (2023) · cites this paper as [150]
In “Biogenesis and Recycling of Synaptic Vesicles at the Neuronal Synapse” (page unavailable), the paper discusses ultrafast endocytosis and bulk endocytosis as mechanisms associated with synaptic vesicle recycling, and links bulk endocytosis to stronger stimulation. It treats them as separate forms, however; it does not identify an “ultrafast bulk endocytosis” mechanism. Its description of the stimulation-linked bulk form is also tentative (“may represent bulk endocytosis”). (LLM, conf=0.84)
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- Authors
- Milosevic, I.
- Venue
- Frontiers in Cellular Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2018-02-06
- Volume
- 12
- Pages
- 27-27
- ISSN
- 1662-5102 (ISSN-L)
- PMC
- PMC5807904
- OpenAlex
- W2791550087
- Cited by
- 122
- References
- 6
- Citations by year
- 2026: 13 · 2025: 10 · 2024: 10 · 2023: 12 · 2022: 10 · 2021: 12 · 2020: 31 · 2019: 14 · 2018: 9
- FWCI
- 1.85
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Cellular Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- GoeScholar The Publication Server of the Georg-August-Universität Göttingen (Georg-August-Universität Göttingen) (submittedVersion, cc-by)
- Funders
- Deutsche Forschungsgemeinschaft (Emmy Noether Young Investigator Award MI-1702/1, SFB889/2/A08 and SFB1190/P02)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Keywords
- clathrin-mediated endocytosis, synaptic vesicle recycling, synaptic vesicle formation, presynaptic terminals, dynamin, kiss-and-run, bulk endocytosis, endosomes, neurotransmission
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