The DOI matches its Crossref record; 157 of the 157 references it cites were found in a registry or an index.
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]
Citations
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Items 201–238 of 238
Correlating Synaptic Ultrastructure and Function at the NanoscalePreprint
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Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosisPreprint
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Pascual-Caro, C., & de Juan‐Sanz, J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.19.590083
“Exocytosis of synaptic vesicles occurs in time scales of seconds, and it is subsequently followed by fast retrieval of exposed proteins back to the intracellular space 2,5,6,29 .”
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Local Glutamate-Glutamine Cycling Underlies Presynaptic ATP Homeostasis
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“Across diverse animal species, presynaptic terminals maintain uniformly small vesicles [18,23–25], suggesting an evolutionarily conserved mechanism for vesicle size regulation.”
Molecular mechanism of synaptic vesicles recycling : role of the Phospholipid Scramblase-1 (PLSCR1)
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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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