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Molecular Circuitry of Endocytosis at Nerve Terminals
Abstract
Presynaptic terminals are specialized compartments of neurons responsible for converting electrical signals into secreted chemicals. This self-renewing process of chemical synaptic transmission is accomplished by the calcium-triggered fusion of neurotransmitter-containing vesicles with the plasma membrane and subsequent retrieval and recycling of vesicle components. Whereas the release of neurotransmitters has been studied for over 50 years, the process of synaptic vesicle endocytosis has remained much more elusive. The advent of imaging techniques suited to monitor membrane retrieval at presynaptic terminals and the discovery of the molecules that orchestrate endocytosis have revolutionized our understanding of this critical trafficking event.
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“After exocytosis, vesicle membrane must be retrieved from the plasma membrane through endocytosis to keep the area of the plasma membrane constant and maintain a sufficient number of synaptic vesicles at presynapses1–4.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [3]
In the citing paper
“After exocytosis, vesicle membrane must be retrieved from the plasma membrane through endocytosis to keep the area of the plasma membrane constant and maintain a sufficient number of synaptic vesicles at presynapses1–4.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [3]
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Calcium Control of Endocytic Capacity at a CNS Synapse
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Research works printed but not linked: 1
- De Camilli P, 2001, Synapses, 217
Cited by
Sorted by citations
Dynamin, a membrane-remodelling GTPase
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“However, endocytosis, and clathrin-mediated endocytosis in particular, also has a specialized role in nerve terminals, mediating the local recycling of synaptic vesicle membranes after exocytosi”
BackgroundActivity-driven local ATP synthesis is required for synaptic function
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“We treat one of the processes driven by calcium signals as the third category: exocytosis of synaptic vesicles and the ensuing synaptic vesicle cycle (Dittman and Ryan, 2009).”
Self-citationUltrafast endocytosis at mouse hippocampal synapses
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“Unlike CME in nonneuronal cells endocytic reformation of SVs in neurons is strictly coupled to stimulation-dependent exocytosis resulting in a wave of endocytic activity (Dittman and Ryan, 2009).”
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“Some general principles apply to clathrinmediated endocytosis in all cellular contexts (Conner and Schmid 2003; Jung and Haucke 2007; Dittman and Ryan 2009; Kirchhausen 2009; McMahon and Boucrot 2011; Taylor et al. 2011).”
Background
Metadata
- Authors
- Dittman, J., & Ryan, T. A.
- Affiliations
- Weill Cornell Medicine (US)
- Venue
- Annual Review of Cell and Developmental Biology
- Publisher
- Annual Reviews
- Published
- 2009-11-01
- Volume
- 25
- Issue
- 1
- Pages
- 133-160
- ISSN
- 1081-0706 (ISSN-L)
- 1530-8995
- OpenAlex
- W2167118899
- Cited by
- 238
- References
- 157
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 5 · 2023: 7 · 2022: 7 · 2021: 8 · 2020: 20 · 2019: 9 · 2018: 6 · 2017: 9 · 2016: 8 · 2015: 22 · 2014: 27 · 2013: 28 · 2012: 28
- FWCI
- 1.85
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Cell and Developmental Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS036942)
- 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
- synaptic vesicle endocytosis, presynaptic terminals, neurotransmitter release, membrane retrieval, vesicle recycling, calcium-triggered exocytosis, synaptic vesicle trafficking, endocytic machinery
- MeSH terms
- Animals, Cell Membrane, Endocytosis, Synapses, Synaptic Vesicles, Presynaptic Terminals
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