Evidence map›Paper›PMID 15117968›Full record

ArticleThe Journal of cell biology2004

Sequential exocytosis of insulin granules is associated with redistribution of SNAP25.

Noriko Takahashi, Hiroyasu Hatakeyama, Haruo Okado, Akiko Miwa, Takuya Kishimoto, Tatsuya Kojima, Teruo Abe, Haruo Kasai

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
  2. A hydrophobic groove in secretagogin allows for alternate interactions with SNAP-25 and syntaxin-4 in endocrine tissues.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Insulin granule biogenesis and exocytosis.Cellular and molecular life sciences : CMLS · 2021
    Review
  7. Review
  8. Article
  9. A Structural View on ESCRT-Mediated Abscission.Frontiers in cell and developmental biology · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Exocytosis, Endocytosis, and Their Coupling in Excitable Cells.Frontiers in molecular neuroscience · 2017
    Review
  19. Article
  20. Insulin secretion from beta cells within intact islets: location matters.Clinical and experimental pharmacology & physiology · 2015
    Review
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

8 authors at 3 institutions in 1 country.

Noriko TakahashiDept. of Cell Physiology, National Institute for Physiological Sciences, Graduate University of Advanced Studies, Myodaiji, Okazaki 444-8585, Japan.
Hiroyasu Hatakeyama
Haruo Okado
Akiko Miwa
Takuya Kishimoto
Tatsuya Kojima
Teruo Abe
Haruo Kasai
National Institute for Physiological Sciences · JPFuchu Hospital · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have investigated sequential exocytosis in beta cells of intact pancreatic islets with the use of two-photon excitation imaging of a polar fluorescent tracer, sulforhodamine B, and a fusion protein comprising enhanced cyan fluorescent protein (ECFP) and the SNARE protein SNAP25 (synaptosome-associated protein of 25 kD) transfected with an adenoviral vector. Sequential exocytosis was found to account for <10% of exocytic events in beta cells stimulated either with glucose under various conditions or by photolysis of a caged-Ca2+ compound. Multigranular exocytosis, in which granule-to-granule fusion occurs before exocytosis, was rarely found. We detected redistribution of ECFP-SNAP25 from the plasma membrane into the membrane of the fused granule occurred in a large proportion (54%) of sequential exocytic events but in only a small fraction (5%) of solitary fusion events. Removal of cholesterol in the plasma membrane by methyl-beta-cyclodextrin facilitated both redistribution of ECFP-SNAP25 and sequential exocytosis by threefold. These observations support the hypothesis that SNAP25 is a plasma membrane factor that is responsible for sequential exocytosis.

Indexed as

beta-CyclodextrinsAnimalsCell MembraneChelating AgentsCyclic AMPCyclodextrinsEgtazic AcidExocytosisFluorescent DyesFura-2GlucoseInsulinInsulin SecretionIslets of LangerhansMembrane FusionMembrane Proteins2-nitrophenyl-EGTAbeta-CyclodextrinsChelating AgentsCyclic AMPCyclodextrinsEgtazic AcidFluorescent DyesFura-2GlucoseInsulinMembrane Proteinsmethyl-beta-cyclodextrinNerve Tissue ProteinsRecombinant Fusion ProteinsSnap25 protein, mouseSynaptosomal-Associated Protein 25Tetradecanoylphorbol Acetate

Identifiers

PMID15117968
PMCPMC2172050
OpenAlexW2102781049

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.