Evidence map›Paper›PMID 24196446›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Inhibition of endocytic vesicle fusion by Plk1-mediated phosphorylation of vimentin during mitosis.

Keisuke Ikawa, Ayaka Satou, Mitsuko Fukuhara, Shigeru Matsumura, Naoyuki Sugiyama, Hidemasa Goto, Mitsunori Fukuda, Masaki Inagaki, Yasushi Ishihama, Fumiko Toyoshima

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Pathophysiological Role of Vimentin Intermediate Filaments in Lung Diseases.Frontiers in cell and developmental biology · 2022
    Review
  5. Article
  6. Article
  7. Posttranslational modifications of the cytoskeleton.Cytoskeleton (Hoboken, N.J.) · 2021
    Review
  8. Article
  9. Intermediate filaments and IF-associated proteins: from cell architecture to cell proliferation.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2019
    Review
  10. Article
  11. Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Keisuke IkawaDepartment of Cell Biology; Institute for Virus Research; Kyoto University; Sakyo-ku, Kyoto, Japan; Department of Mammalian Regulatory Network; Graduate School of Biostudies; Kyoto University; Sakyo-ku, Kyoto, Japan.
Ayaka SatouDepartment of Molecular & Cellular BioAnalysis; Graduate School of Pharmaceutical Sciences; Kyoto University; Sakyo-ku, Kyoto, Japan.
Mitsuko FukuharaDepartment of Cell Biology; Institute for Virus Research; Kyoto University; Sakyo-ku, Kyoto, Japan; Department of Mammalian Regulatory Network; Graduate School of Biostudies; Kyoto University; Sakyo-ku, Kyoto, Japan.
Shigeru MatsumuraDepartment of Cell Biology; Institute for Virus Research; Kyoto University; Sakyo-ku, Kyoto, Japan; Department of Mammalian Regulatory Network; Graduate School of Biostudies; Kyoto University; Sakyo-ku, Kyoto, Japan.
Naoyuki SugiyamaDepartment of Molecular & Cellular BioAnalysis; Graduate School of Pharmaceutical Sciences; Kyoto University; Sakyo-ku, Kyoto, Japan.
Hidemasa GotoDivision of Biochemistry; Aichi Cancer Center Research Institute; Chikusa-ku, Nagoya, Japan.
Mitsunori FukudaDepartment of Developmental Biology and Neurosciences; Graduate School of Life Sciences; Tohoku University; Sendai, Miyagi, Japan.
Masaki InagakiDivision of Biochemistry; Aichi Cancer Center Research Institute; Chikusa-ku, Nagoya, Japan.
Yasushi IshihamaDepartment of Molecular & Cellular BioAnalysis; Graduate School of Pharmaceutical Sciences; Kyoto University; Sakyo-ku, Kyoto, Japan.
Fumiko ToyoshimaDepartment of Cell Biology; Institute for Virus Research; Kyoto University; Sakyo-ku, Kyoto, Japan; Department of Mammalian Regulatory Network; Graduate School of Biostudies; Kyoto University; Sakyo-ku, Kyoto, Japan.
Aichi Cancer Center · JPBaruch S. Blumberg Institute · USKumamoto University · JPKyoto University · JPKyoto Pharmaceutical University · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endocytic vesicle fusion is inhibited during mitosis, but the molecular pathways that mediate the inhibition remain unclear. Here we uncovered an essential role of Polo-like kinase 1 (Plk1) in this mechanism. Phosphoproteomic analysis revealed that Plk1 phosphorylates the intermediate filament protein vimentin on Ser459, which is dispensable for its filament formation but is necessary for the inhibition of endocytic vesicle fusion in mitosis. Furthermore, this mechanism is required for integrin trafficking toward the cleavage furrow during cytokinesis. Our results thus identify a novel mechanism for fusion inhibition in mitosis and implicate its role in vesicle trafficking after anaphase onset.

Indexed as

AnaphaseCell Cycle ProteinsCytokinesisHeLa CellsHumansMitosisPhosphorylationPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsTransport VesiclesVimentinCell Cycle ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsVimentinendosomemitosisPlk1vesicle fusionvimentin

Identifiers

PMID24196446
PMCPMC3925722
OpenAlexW2060719316

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.