Cited by 93Cellular transport and secretionNeuroscience and Neuropharmacology ResearchExtracellular vesicles in disease

Calcium Control of Endocytic Capacity at a CNS Synapse

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Balaji, J., Armbruster, M., Ryan, T. A.·2008·Journal of Neuroscience

Abstract

The ability to recycle synaptic vesicles is a crucial property of nerve terminals that allows maintenance of synaptic transmission. Using high-sensitivity optical approaches at hippocampal nerve terminals in dissociated neurons in culture, we show that modulation of endocytosis can be achieved by expansion of the endocytic capacity. Our experiments indicate that the endocytic capacity, the maximum number of synaptic vesicles that can be internalized in parallel at individual synapses, is tightly controlled by intracellular calcium levels. Increasing levels of intracellular calcium, which occurs as firing frequency increases, significantly increases the endocytic capacity. At physiological temperature after 30 Hz firing, these synapses are capable of endocytosing at least approximately 28 vesicles in parallel, each with a time constant of approximately 6 s. This calcium-dependent control of endocytic capacity reveals a potentially useful adaptive response to high-frequency activity to increase endocytic rates under conditions of vesicle pool depletion.

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Crossref · 10.1523/jneurosci.1082-08.2008

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  • When ultrafast endocytosis is blocked, a slow clathrin-mediated endocytic pathway can kick in.

    “When ultrafast endocytosis is blocked, a slow clathrin-mediated endocytic pathway can kick in7 - this is consistent with observations from live-cell imaging of endocytosis68–70.”

    From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [69]

    The Introduction describes vesicle retrieval with a mean time of about 14 seconds, and the Discussion describes the process studied as clathrin-dependent. But the paper does not report that blocking ultrafast endocytosis causes a slow clathrin-mediated pathway to take over; it instead proposes a single endocytic mode with calcium-controlled capacity. The indexed passages provide no page numbers. (LLM, conf=0.82)

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Authors
Balaji, J., Armbruster, M., & Ryan, T. A.
Affiliations
  • Weill Cornell Medicine (US)
  • Cornell University (US)
Corresponding author
Ryan, T. A.
Venue
Journal of Neuroscience
Published
2008-06-25
Volume
28
Issue
26
Pages
6742-6749
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2063912923
Cited by
93
References
1
Citations by year
2026: 1 · 2025: 2 · 2023: 4 · 2022: 6 · 2020: 2 · 2019: 2 · 2018: 3 · 2017: 4 · 2016: 4 · 2015: 4 · 2014: 7 · 2013: 12 · 2012: 8
FWCI
4.96
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • 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
endocytosis, synaptic vesicle recycling, intracellular calcium, hippocampal synapses, synaptic transmission, firing rate, calcium-dependent regulation, high-frequency activity
MeSH terms
Action Potentials, Animals, Animals, Newborn, Calcium, Cells, Cultured, Endocytosis, Fluorescent Dyes, Hippocampus, Nerve Tissue Proteins, Synaptic Transmission, Synapses, Synaptic Vesicles, Rats, Sprague-Dawley, Presynaptic Terminals, Neurotransmitter Agents, Microscopy, Confocal, Calcium Signaling, Rats

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