Evidence map›Paper›PMID 12598621›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2003

Bulk membrane retrieval in the synaptic terminal of retinal bipolar cells.

Matthew Holt, Anne Cooke, Minnie M Wu, Leon Lagnado

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

104 citing papers in PubMed, 181 citations in OpenAlex.

  1. Article
  2. Review
  3. Mechanical stretch regulates macropinocytosis inMolecular biology of the cell · 2024
    Article
  4. Article
  5. Review
  6. Multiple Roles of Actin in Exo- and Endocytosis.Frontiers in synaptic neuroscience · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Activity and Cytosolic NaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. On the existence of endocytosis driven by membrane phase separations.Biochimica et biophysica acta. Biomembranes · 2020
    Review
  14. Review
  15. Review
  16. Activity-dependent bulk endocytosis proteome reveals a key presynaptic role for the monomeric GTPase Rab11.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Article
  18. Synaptic Vesicle Endocytosis in Different Model Systems.Frontiers in cellular neuroscience · 2018
    Review
  19. Review
  20. Review

44 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Matthew HoltMedical Research Council Laboratory of Molecular Biology, Cambridge CB2 2QH, United Kingdom.
Anne Cooke
Minnie M Wu
Leon Lagnado
MRC Laboratory of Molecular Biology · GBMedical Research Council · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanism of bulk membrane uptake at the synapse remains poorly defined, although exocytosis of synaptic vesicles is followed by compensatory membrane retrieval into both small vesicles and large cisternas or vacuoles. We investigated bulk retrieval in the presynaptic terminal of retinal bipolar cells. Fluorescence imaging of the membrane dye FM1-43 indicated that Ca2+-triggered exocytosis was followed by endocytosis into small vesicles and larger vacuoles that could be selectively labeled using large fluorescent dextrans. Disruption of actin filaments with cytochalasin D or latrunculin B inhibited the formation and transport of vacuoles, but exocytosis and endocytosis continued at normal rates. Bulk retrieval was linked to remodeling of the actin network, and both processes were inhibited by 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one, an inhibitor of phosphatidylinositol 3-kinase (PI 3-kinase). The regulation of F-actin dynamics by Ca2+ and PI 3-kinase therefore played an important role in compensatory endocytosis at this synapse, but this role was confined to bulk membrane uptake. Capacitance measurements demonstrated that fast endocytosis and refilling of the rapidly releasable pool of vesicles were not dependent on F-actin or PI 3-kinase activity. The basic properties of bulk membrane retrieval at this synapse were very similar to macropinocytosis described in non-neural cells. Bulk retrieval did not play an essential role in maintaining the vesicle cycle during maintained stimulation, but we suggest that it may play a role in the structural plasticity of this synaptic terminal.

Indexed as

EndocytosisActin CytoskeletonAnimalsBiological TransportCalciumCell CompartmentationCell MembraneCells, CulturedDextransGoldfishKineticsMicroscopy, FluorescencePhosphatidylinositol 3-KinasesPinocytosisPresynaptic TerminalsRetinaCalciumDextransPhosphatidylinositol 3-Kinases

Identifiers

PMID12598621
PMCPMC6742272
OpenAlexW1886198059

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.