The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Ultrafast endocytosis at mouse hippocampal synapses
Open accessAbstract
To sustain neurotransmission, synaptic vesicles and their associated proteins must be recycled locally at synapses. Synaptic vesicles are thought to be regenerated approximately 20 s after fusion by the assembly of clathrin scaffolds or in approximately 1 s by the reversal of fusion pores via 'kiss-and-run' endocytosis. Here we use optogenetics to stimulate cultured hippocampal neurons with a single stimulus, rapidly freeze them after fixed intervals and examine the ultrastructure using electron microscopy--'flash-and-freeze' electron microscopy. Docked vesicles fuse and collapse into the membrane within 30 ms of the stimulus. Compensatory endocytosis occurs within 50 to 100 ms at sites flanking the active zone. Invagination is blocked by inhibition of actin polymerization, and scission is blocked by inhibiting dynamin. Because intact synaptic vesicles are not recovered, this form of recycling is not compatible with kiss-and-run endocytosis; moreover, it is 200-fold faster than clathrin-mediated endocytosis. It is likely that 'ultrafast endocytosis' is specialized to restore the surface area of the membrane rapidly.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Several recent studies suggest that synaptic vesicle endocytosis is mediated by clathrin-independent ultrafast endocytosis at mammalian central synapses and is tightly coupled to exocytosis in time and space5–9.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Thus, the actin ring surrounding the active zone is likely essential for ultrafast endocytosis5.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Indeed, ultrafast endocytosis initiates as fast as 20–50 ms after exocytosis and completes within 100 ms5–7.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In this pathway, endocytic invaginations always form at the edge of the active zone5–7.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Following exocytosis, synaptic vesicles are recovered through clathrin-mediated, ultrafast, bulk, or kiss-and-run endocytic pathways.”
From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [32]
Experimental — accuracy not yet measured
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Ultrafast endocytosis occurs rapidly, within 50–100 milliseconds following stimulation, capturing approximately four vesicles at the very edge of the active zone [32]. This mechanism is specialized for rapidly restoring the surface area of the presynaptic membrane and is kinetically distinct from both kiss-and-run and clathrin-mediated endocytosis [33].”
From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [32]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Several recent studies suggest that synaptic vesicle endocytosis is mediated by clathrin-independent ultrafast endocytosis at mammalian central synapses and is tightly coupled to exocytosis in time and space5–9.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
The cited source says what the claim attributes to it.
In the citing paper
“Consistent with our previous work5, treatment with DMSO (control) did not affect ultrafast endocytosis, while Latrunculin A treatment completely blocked it (Fig. 2c, d; more micrographs in Supplementary Fig. 4).”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
The cited source says what the claim attributes to it.
In the citing paper
“Importantly, the timing and the location of endocytic pit formation quantitatively recapitulates endocytic events observed by ultrastructural analysis5,6.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
The cited source says what the claim attributes to it.
In the citing paper
“Filamentous actin (F-actin) is essential for the initiation of ultrafast endocytosis5.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
The cited source says what the claim attributes to it.
In the citing paper
“When neurons are treated with Latrunculin A, which sequesters monomeric actin (G-actin) and perturbs F-actin formation12,13, ultrafast endocytosis fails completely, with no induction of membrane pit formation5.”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
The cited source says what the claim attributes to it.
In the citing paper
“Interestingly, ultrafast endocytosis is compensatory - the membrane area of endocytic vesicles is roughly equal to the total surface area of synaptic vesicles exocytosed5,6”
From Membrane compression by synaptic vesicle exocytosis triggers ultrafast endocytosis (2023) · cites this paper as [5]
The cited source says what the claim attributes to it.
In the citing paper
“Kiss-and-run is a rapid mechanism that involves a transient opening of a fusion pore, allowing for neurotransmitter release without full collapse of the SV into the plasma membrane [30]. The vesicle is then rapidly retrieved, often within approximately one second [31,32].”
From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [32]
The cited source says what the claim attributes to it.
In the citing paper
“Key proteins involved include clathrin itself and dynamin, which mediates the scission of the budding vesicle from the plasma membrane [32].”
From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [32]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Computer Visualization of Three-Dimensional Image Data Using IMOD
Kremer, J. R., Mastronarde, D. N., & McIntosh, J. R. (1996) · Journal of Structural Biology · doi:10.1006/jsbi.1996.0013 · Cited by 5,530
Molecular mechanism and physiological functions of clathrin-mediated endocytosis
McMahon, H. T., & Boucrot, E. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3151 · Cited by 2,223
Heuser, J. E., & Reese, T. S. (1973) · The Journal of Cell Biology · doi:10.1083/jcb.57.2.315 · Cited by 2,147
Germline Transmission and Tissue-Specific Expression of Transgenes Delivered by Lentiviral Vectors
Lois, C., Hong, E. J., Pease, S., Brown, E. J., & Baltimore, D. (2002) · Science · doi:10.1126/science.1067081 · Cited by 1,992
Dynasore, a Cell-Permeable Inhibitor of Dynamin
Macia, E., Ehrlich, M., Massol, R., Boucrot, E., Brunner, C., & Kirchhausen, T. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.04.002 · Cited by 1,958
TrakEM2 Software for Neural Circuit Reconstruction
Cardona, A., Saalfeld, S., Schindelin, J., Arganda‐Carreras, I., Preibisch, S., Longair, M., Tomančák, P., Hartenstein, V., & Douglas, R. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038011 · Cited by 1,009
Gunaydin, L. A., Yizhar, O., Berndt, A., Sohal, V. S., Deisseroth, K., & Hegemann, P. (2010) · Nature Neuroscience · doi:10.1038/nn.2495 · Cited by 757
Latrunculins: Novel Marine Toxins That Disrupt Microfilament Organization in Cultured Cells
Spector, I., Shochet, N. R., Kashman, Y., & Groweiss, A. (1983) · Science · doi:10.1126/science.6681676 · Cited by 750
Granseth, B., Odermatt, B., Royle, S. J., & Lagnado, L. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.029 · Cited by 686
Varoqueaux, F., Sigler, A., Rhee, J.-S., Brose, N., Enk, C., Reim, K., & Rosenmund, C. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122623799 · Cited by 619
Self-citation
Cited by
Sorted by citations
Items 501–600 of 607
Wen, X. (2018) · DigitalCommons@UNMC
ATP Depletion Impairs Activity-dependent Ultrafast Endocytosis at Hippocampal Synapses
Gan, Q., & Watanabe, S. (2018) · Microscopy and Microanalysis · doi:10.1017/s1431927618007043
Self-citationChen, R. (2017) · TSpace (University of Toronto)
Terada, H., Saitoh, Y., Kametani, K., Sakaguchi, M., Sakamoto, T., Kamijo, A., & Terada, N. (2018) · Microscopy Research and Technique · doi:10.1002/jemt.23166
Study of a kinesin adaptor in axonal transport and synapse formation
Dehaghi, T. K. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7310
Role of Alix in endocytosis at presynaptic boutons
Chi, K. (2019) · theses.fr (ABES) · doi:10.70675/7ca1e50bza1d0z4d91z8220z02171a9bfb97
The endolysosomal system in neuronal physiology and pathology
Sanchez, S. V. (2019)
A JOURNEY TOWARDS UNDERSTANDING BIOLOGY HOLISTICALLY AT THE NANOSCALE
Moser, T. H. (2018) · Digital Commons - Michigan Tech (Michigan Technological University) · doi:10.37099/mtu.dc.etdr/739
Mechanisms of synaptic plasticity mediated by Clathrin Adaptor-protein complexes 1 and 2 in mice
Mishra, R. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7514
Redlingshöfer, L., McLeod, F., Camus, M., Chen, Y., Burden, J., Vila, E. P., Briant, K., Dannhauser, P. N., Salinas, P., & Brodsky, F. (2019) · bioRxiv · doi:10.1101/815183 · Cited by 2
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.007
X-Ray Microscope Instrumentation
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.008
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.004
Morphological Studies of Synaptic Vesicle Recycling at the Inner Hair Cell Ribbon Synapse
Kroll, J. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7800
Electron microscopy of plant samples by using high-pressure freezing/freeze substitution method
Sato, M., Wakazaki, M., Goto, Y., & Toyooka, K. (2019) · PLANT MORPHOLOGY · doi:10.5685/plmorphol.31.25
Scaffolding Mechanisms Supporting Fast Neurotransmitter Release at the Presynaptic Active Zone
Held, R. G. (2018) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.003
X-Ray Microscopes: a Short Introduction
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.002
Faculty Opinions recommendation of Synaptic vesicles transiently dock to refill release sites.
Klyachko, V. A. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738749520.793583444
Appendix A X-Ray Data Tabulations
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.014
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.011
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.005
Jacobsen, C. J. (2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.001
(2019) · Cambridge University Press eBooks · doi:10.1017/9781139924542.015
A quantitative analysis of an average cultured neuron
Jähne, S. (2020) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7934
Olsthoorn, H. M. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8919
Long-Term Temporal Dynamics of Synaptic Vesicles
Truckenbrodt, S. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6481
Post-Translational Protein Modifications involved in Exo- and Endocytosis of Synaptic Vesicles
Silbern, I. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8895
Erythropoietin-mediated neuroprotection in insects
Miljus, N. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5834
Targeting ion sensors to synaptic vesicles using a Nanobody against luminal Synaptotagmin 1
Goel, R. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-51
Kohansal-Nodehi, M. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6118
Faculty Opinions recommendation of Critical role for Piccolo in synaptic vesicle retrieval.
Mizumoto, K., & Kurashina, M. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735737585.793563402
Mayor, S., & Hemalatha, A. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733515523.793555324
Faculty Opinions recommendation of Synaptic vesicles transiently dock to refill release sites.
Chapman, E. R., & Vevea, J. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738749520.793581127
Faculty Opinions recommendation of Cell membranes resist flow.
Bradke, F., & Lin, T.-C. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734323511.793564815
Isacoff, E. Y., & Reiner, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.20100-4
Faculty Opinions recommendation of Synaptic vesicles transiently dock to refill release sites.
Brodin, L. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738749520.793578967
Isacoff, E. Y., & Reiner, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00150-4
Synaptosomes and Synaptic Vesicles
Stunault, M. I., & Ashrafi, G. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00215-7
Revealing ultrastructural changes that determine the development of a CNS synapse
Hintze, A. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9828
Canales, M. R. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9984
Excitation-Secretion Coupling of Dense-Core Vesicle Release
Cirkovic, V. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10009
Mahapatra, S., & Takahashi, T. (2023) · eLife · doi:10.7554/elife.90497.1
Rho GTPase signaling and mDia facilitate endocytosis via presynaptic actinPreprint
Oevel, K., Hohensee, S., Kumar, A., Rosas-Brugada, I., Bartolini, F., Soykan, T., & Haucke, V. (2023) · eLife · doi:10.7554/elife.92755.1
Characterization of factors affecting synaptic transmission in C. elegans
Jánosi, B. (2023) · Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) · doi:10.21248/gups.81189
Implication du récepteur de mort Fas dans la formation et la sécrétion de vésicules extracellulaires
Servant, Z. (2023) · theses.fr (ABES) · doi:10.70675/806a7bffzaf30z4270zaed8z5434904da10e
Mahapatra, S., & Takahashi, T. (2024) · eLife · doi:10.7554/elife.90497.2
Rôle des microARNs dans le contrôle de l'hypersécrétion par les tumeurs neuroendocrines.
Drissa, I. (2023) · theses.fr (ABES) · doi:10.70675/926a0c53z1252z4d63za9fcz204e10cfb66d
Presynaptic plasticity is associated with actin polymerization
Kudryashova, I. V. (2023) · Biochemistry (Moscow) · doi:10.31857/s0320972523030089
Shishkov, A. G., Nifantova, N. V., Korenkova, O. M., Sopova, E., Brodin, L., & Shupliakov, O. (2023) · Биологические мембраны Журнал мембранной и клеточной биологии · doi:10.31857/s0233475523030088
Endosomal sorting protein SNX4 limits synaptic vesicle docking and releasePreprint
Poppinga, J., Barret, N. J., Cornelisse, L. N., Verhage, M., & van Weering, J. R. T. (2024) · eLife · doi:10.7554/elife.97910.1
Mahapatra, S., & Takahashi, T. (2024) · eLife · doi:10.7554/elife.90497.3
Toulmé, E., Murach, J., Bärfuss, S., Kroll, J., Malsam, J., Trimbuch, T., Herman, M. A., Söllner, T. H., & Rosenmund, C. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0076-24.2024
Self-citationAinatzi, S. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10653
Zobel, S., & Rosenmund, C. (2024) · Neuromethods · doi:10.1007/978-1-0716-4019-7_14
Self-citationA Technique to Perform Structure–Function Analysis of Synapses
Wichmann, C., & Michanski, S. (2024) · Neuromethods · doi:10.1007/978-1-0716-4019-7_5
Endosomal sorting protein SNX4 limits synaptic vesicle docking and releasePreprint
Poppinga, J., Barret, N. J., Cornelisse, L. N., Verhage, M., & van Weering, J. R. T. (2024) · eLife · doi:10.7554/elife.97910.2
Liu, J., & Ha, T. (2024) · Biophysical Journal · doi:10.1016/j.bpj.2024.11.3308
Song, M., Park, H. Y., Kim, H. J., & Kwon, S. (2025) · Biomaterials Science · doi:10.1039/d4bm01661k
Kahms, M., Pandey, S., & Klingauf, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.31.646354
Emperador-Melero, J., Signore, S. J. D., González, K. M. D. L., Kaeser, P. S., & Rodal, A. A. (2026) · eLife · doi:10.7554/elife.107276.3
Emperador-Melero, J., Signore, S. J. D., González, K. M. D. L., Kaeser, P. S., & Rodal, A. A. (2025) · eLife · doi:10.7554/elife.107276
Emperador-Melero, J., Signore, S. J. D., González, K. M. D. L., Kaeser, P. S., & Rodal, A. A. (2025) · eLife · doi:10.7554/elife.107276.1
Lichter, K. (2025) · Science · doi:10.1126/science.aec0091
Bowers, M. R., Shields, M. C., & Reist, N. E. (2025) · Elsevier eBooks · doi:10.1016/b978-0-12-811114-7.00021-9
Dynamin Is a Key Molecule to Decode Action Potential Firing
Tanifuji, S., & Mochida, S. (2014) · Springer eBooks · doi:10.1007/978-4-431-55166-9_11
Synaptotagmin 1-triggered lipid signaling couples exo- and endocytosis
Bolz, S. (2023) · Refubium (Universitätsbibliothek der Freien Universität Berlin) · doi:10.17169/refubium-41946
Presynaptic function of the voltage-gated calcium channel DmCa1D in Drosophila larval motoneurons
Klein, A. (2016) · Gutenberg Open Science · doi:10.25358/openscience-2767
Shining Light On An Amygdala -- Brainstem Connection Important For Attention Processing
Cano, J. C. (2019) · DigitalCommons@UTEP (The University of Texas at El Paso)
Hexokinase-1 Activity Modulates Synaptic Vesicle Docking but not Endocytic RecyclingPreprint
Liang, Y. (2025) · Research Square · doi:10.21203/rs.3.rs-8080809/v1
Identification of the SNARE proteins involved in the postsynaptic membrane trafficking
Krapivkina, J. (2016) · theses.fr (ABES) · doi:10.70675/f9577921z306ez4d54za97bz8cb4fde3f7f8
Visualisation and Perturbation of the Spatio-Temporal Dynamics of Endocytosis
Rosendale, M. (2015) · theses.fr (ABES) · doi:10.70675/c43e8a79z3005z46daz8eb6z6d7ab3a61888
McFadden, M. H. (2018) · theses.fr (ABES) · doi:10.70675/036294d9z53a4z495ez9221ze4fba667c298
Comment les lipides polyinsaturés facilitent les déformations membranaires
Tiberti, M. L. (2019) · theses.fr (ABES) · doi:10.70675/75b094b2zea60z4425za9a7zeeb330bb5279
Polyunsaturated phospholipids in large-scale membrane deformations induced by bacterial toxins
Tsai, M.-C. (2020) · theses.fr (ABES) · doi:10.70675/40a8087fzd0eaz41e2z8fb4z2ae6960e5173
Roles of actin nanostructures in presynaptic assembly and function
Bingham, D. (2022) · theses.fr (ABES) · doi:10.70675/3429ee4azbae8z4db7zbd5bzaa1e84716d71
Ultrastructural and molecular analysis of cortico-striatal dopamine hub synapses
Lapios, P. (2024) · theses.fr (ABES) · doi:10.70675/527646a6zd9b5z4935z80ebz0950bba9d08e
Deciphering the role of Creatine Kinase B in energy supply for fast axonal transport
Cuoc, E. C. (2023) · theses.fr (ABES) · doi:10.70675/707730b1zcba0z4c17zbf1az4471b4140440
Physiological implications of phase separation in vesicle organization and trafficking
Liu, C., Cheng, J., & Wu, X. (2026) · BMC Biology · doi:10.1186/s12915-026-02607-6
Dissecting the role of EPS15 and EPS15R in the mammalian brain
Shergill, J. K. (2026) · Publication Server of Kaiserslautern University of Technology (Kaiserslautern University of Technology) · doi:10.26204/kluedo/13063
Mechanisms of presynaptic dysfunction in rodent models of epilepsy
Hogg, J. (2026) · ERA · doi:10.7488/era/7202
Membrane Merger Dynamics in Exocytosis and Endocytosis
Guo, X., Chan, C. Y., & Wu, L. (2026) · Advances in experimental medicine and biology · doi:10.1007/978-3-032-22637-2_3
Biology and physiology of synaptic vesicle clusters
Brodin, L., & Shupliakov, O. (2026) · Trends Open · doi:10.1016/j.treopn.2026.04.006
Lv, Z.-Y., Lu, Z.-H., Liu, S., Zhou, P., Lau, P.-M., Bi, G., & Tao, C.-L. (2026) · Neuroscience Bulletin · doi:10.1007/s12264-026-01646-x
Contri, A., Francis, E. A., Massing, A., & Rangamani, P. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.03.736361
Functional Specialization of Clathrin‐Independent Endocytic Routes: Mechanisms and Cellular Roles
Benvenuto, A. F., Fardin, A., Balestra, M., Fiore, P. P. D., Tordonato, C., & Sigismund, S. (2026) · Traffic · doi:10.1111/tra.70049
Metadata
- Authors
- Watanabe, S., Rost, B. R., Camacho-Pérez, M., Davis, M. W., Söhl-Kielczynski, B., Rosenmund, C., & Jorgensen, E. M.
- Affiliations
- Howard Hughes Medical Institute (US)
- Charité – Universitätsmedizin Berlin (DE)
- Corresponding author
- Rosenmund, Christian
- Venue
- Nature
- Published
- 2013-12-04
- Volume
- 504
- Issue
- 7479
- Pages
- 242-247
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3957339
- OpenAlex
- W2093450191
- Cited by
- 607
- References
- 54
- Citations by year
- 2026: 26 · 2025: 40 · 2024: 44 · 2023: 47 · 2022: 53 · 2021: 44 · 2020: 53 · 2019: 62 · 2018: 51 · 2017: 54 · 2016: 36 · 2015: 58 · 2014: 38 · 2013: 1
- FWCI
- 25.72
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DZNE Pub (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute of Neurological Disorders and Stroke (R37NS034307, NS034307, R01NS034307)
- 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 recycling, clathrin-mediated endocytosis, dynamin, actin polymerization, hippocampal synapses, neurotransmission, membrane internalization, active zone, optogenetic stimulation
- MeSH terms
- Actins, Action Potentials, Animals, Endocytosis, Exocytosis, Hippocampus, Membrane Fusion, Microscopy, Electron, Synaptic Transmission, Rhodopsin, Synapses, Synaptic Vesicles, Time Factors, Dynamins, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review