Evidence map›Paper›PMID 28414717›Full record

ArticlePLoS biology2017

A Ca2+ channel differentially regulates Clathrin-mediated and activity-dependent bulk endocytosis.

Chi-Kuang Yao, Yu-Tzu Liu, I-Chi Lee, You-Tung Wang, Ping-Yen Wu

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

32 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. The human Flower isoform hFWE4 facilitates cornification in cutaneous squamous cell carcinoma.JID innovations : skin science from molecules to population health · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Biomechanics-mediated endocytosis in atherosclerosis.Frontiers in cardiovascular medicine · 2024
    Review
  9. The epithelial NaCell reports · 2023
    Article
  10. The SphK1/S1P Axis Regulates Synaptic Vesicle Endocytosis via TRPC5 Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Rlip76: An Unexplored Player in Neurodegeneration and Alzheimer's Disease?International journal of molecular sciences · 2022
    Review
  16. Article
  17. Frontiers in plant science · 2022
    Article
  18. Article
  19. Inhibiting endocytosis in CGRPNature communications · 2021
    Article
  20. Article
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

5 authors at 2 institutions in 1 country.

Chi-Kuang YaoInstitute of Biological Chemistry, Academia Sinica, Nankang, Taipei, Taiwan.ORCID 0000-0003-0977-4347
Yu-Tzu LiuInstitute of Biological Chemistry, Academia Sinica, Nankang, Taipei, Taiwan.
I-Chi LeeInstitute of Biological Chemistry, Academia Sinica, Nankang, Taipei, Taiwan.
You-Tung WangInstitute of Biological Chemistry, Academia Sinica, Nankang, Taipei, Taiwan.
Ping-Yen WuInstitute of Biological Chemistry, Academia Sinica, Nankang, Taipei, Taiwan.
Institute of Biological Chemistry, Academia Sinica · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clathrin-mediated endocytosis (CME) and activity-dependent bulk endocytosis (ADBE) are two predominant forms of synaptic vesicle (SV) endocytosis, elicited by moderate and strong stimuli, respectively. They are tightly coupled with exocytosis for sustained neurotransmission. However, the underlying mechanisms are ill defined. We previously reported that the Flower (Fwe) Ca2+ channel present in SVs is incorporated into the periactive zone upon SV fusion, where it triggers CME, thus coupling exocytosis to CME. Here, we show that Fwe also promotes ADBE. Intriguingly, the effects of Fwe on CME and ADBE depend on the strength of the stimulus. Upon mild stimulation, Fwe controls CME independently of Ca2+ channeling. However, upon strong stimulation, Fwe triggers a Ca2+ influx that initiates ADBE. Moreover, knockout of rodent fwe in cultured rat hippocampal neurons impairs but does not completely abolish CME, similar to the loss of Drosophila fwe at the neuromuscular junction, suggesting that Fwe plays a regulatory role in regulating CME across species. In addition, the function of Fwe in ADBE is conserved at mammalian central synapses. Hence, Fwe exerts different effects in response to different stimulus strengths to control two major modes of endocytosis.

Indexed as

AnimalsAnimals, Genetically ModifiedCalciumCalcium ChannelsCell LineClathrinDrosophila ProteinsEndocytosisExocytosisGene Knockdown TechniquesLanthanumMiceMutationNeuronsProtein IsoformsRatsCacfd1 protein, ratCalciumCalcium ChannelsClathrinDrosophila ProteinsFlower protein, mousefwe protein, DrosophilaLanthanumProtein Isoforms

Identifiers

PMID28414717
PMCPMC5393565
OpenAlexW2606361886

What OpenQuestion holds

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LicenceCC BY
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.