Evidence map›Paper›PMID 28674075›Full record

ArticleJournal of cell science2017

Clathrin-mediated post-fusion membrane retrieval influences the exocytic mode of endothelial Weibel-Palade bodies.

Nicola L Stevenson, Ian J White, Jessica J McCormack, Christopher Robinson, Daniel F Cutler, Thomas D Nightingale

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2017. 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
1.4field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Tip-end fusion of a rod-shaped secretory organelle.Cellular and molecular life sciences : CMLS · 2022
    Article
  4. Spire1 and Myosin Vc promote CaCellular and molecular life sciences : CMLS · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Exocytosis of Weibel-Palade bodies: how to unpack a vascular emergency kit.Journal of thrombosis and haemostasis : JTH · 2019
    Review
  12. 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

6 authors at 3 institutions in 1 country.

Nicola L StevensonMRC Cell Biology Unit, Laboratory of Molecular Cell Biology, University College London, Gower Street, London, WC1E 6BT, UK.
Ian J WhiteMRC Cell Biology Unit, Laboratory of Molecular Cell Biology, University College London, Gower Street, London, WC1E 6BT, UK.
Jessica J McCormackMRC Cell Biology Unit, Laboratory of Molecular Cell Biology, University College London, Gower Street, London, WC1E 6BT, UK.
Christopher RobinsonCentre for Microvascular Research, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Daniel F CutlerMRC Cell Biology Unit, Laboratory of Molecular Cell Biology, University College London, Gower Street, London, WC1E 6BT, UK t.nightingale@qmul.ac.uk d.cutler@ucl.ac.uk.ORCID http://orcid.org/0000-0002-4288-7530
Thomas D NightingaleCentre for Microvascular Research, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK t.nightingale@qmul.ac.uk d.cutler@ucl.ac.uk.
MRC Laboratory for Molecular Cell Biology · GBQueen Mary University of London · GBUniversity of Bristol · GB

Funding

British Heart Foundation PG/15/72/31732Medical Research Council MC_UU_00012/2Medical Research Council MC_UU_12018/2Medical Research Council MR/M019179/1Medical Research Council MR/M02492X/1
6 · The paper itself

Abstract

Weibel-Palade bodies (WPBs), the storage organelles of endothelial cells, are essential to normal haemostatic and inflammatory responses. Their major constituent protein is von Willebrand factor (VWF) which, following stimulation with secretagogues, is released into the blood vessel lumen as large platelet-catching strings. This exocytosis changes the protein composition of the cell surface and also results in a net increase in the amount of plasma membrane. Compensatory endocytosis is thought to limit changes in cell size and retrieve fusion machinery and other misplaced integral membrane proteins following exocytosis; however, little is known about the extent, timing, mechanism and precise function of compensatory endocytosis in endothelial cells. Using biochemical assays, live-cell imaging and correlative spinning-disk microscopy and transmission electron microscopy assays we provide the first in-depth high-resolution characterisation of this process. We provide a model of compensatory endocytosis based on rapid clathrin- and dynamin-mediated retrieval. Inhibition of this process results in a change of exocytic mode: WPBs then fuse with previously fused WPBs rather than the plasma membrane, leading, in turn, to the formation of structurally impaired tangled VWF strings.This article has an associated First Person interview with the first authors of the paper.

Indexed as

ClathrinExocytosisHumansHuman Umbilical Vein Endothelial CellsMembrane FusionWeibel-Palade BodiesClathrinClathrinDynaminEndocytosisEndotheliumExocytosisWeibel-Palade bodies

Identifiers

PMID28674075
PMCPMC5558267
OpenAlexW2724305689

What OpenQuestion holds

Textmetadata
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.