Evidence map›Paper›PMID 15004223›Full record

ArticleMolecular biology of the cell2004

Uncoated endocytic vesicles require the unconventional myosin, Myo6, for rapid transport through actin barriers.

Laura Aschenbrenner, Samia N Naccache, Tama Hasson

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.7field-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

50 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Myosin-Driven Intracellular Transport.Cold Spring Harbor perspectives in biology · 2018
    Review
  10. Article
  11. Investigations of human myosin VI targeting using optogenetically controlled cargo loading.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Transmembrane protein 55B is a novel regulator of cellular cholesterol metabolism.Arteriosclerosis, thrombosis, and vascular biology · 2014
    Article
  20. Myosin lever arm directs collective motion on cellular actin network.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

3 authors at 1 institution in 1 country.

Laura AschenbrennerSection of Cell and Developmental Biology, Division of Biological Sciences, University of California at San Diego, La Jolla, California 92093, USA.
Samia N Naccache
Tama Hasson
University of California San Diego · US

Funding

MOLECULAR DISSECTION OF MYOSIN VIIAR01EY012695 · NEI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI HASSON, TAMA W · 2001 to 2004
$1.1M
NEI NIH HHS R01 EY012695NEI NIH HHS R01 EY 12695
6 · The paper itself

Abstract

After clathrin-mediated endocytosis, clathrin removal yields an uncoated vesicle population primed for fusion with the early endosome. Here we present the first characterization of uncoated vesicles and show that myo6, an unconventional myosin, functions to move these vesicles out of actin-rich regions found in epithelial cells. Time-lapse microscopy revealed that myo6-associated uncoated vesicles were motile and exhibited fusion and stretching events before endosome delivery, processes that were dependent on myo6 motor activity. In the absence of myo6 motor activity, uncoated vesicles remained trapped in the actin mesh, where they exhibited Brownian-like motion. Exit from the actin mesh occurred by a slow diffusion-based mechanism, delaying transferrin trafficking to the early endosome. Expression of a myo6 mutant that bound tightly to F-actin produced immobilized vesicles and blocked trafficking. Depolymerization of the actin cytoskeleton rescued this block and specifically accelerated transferrin delivery to the early endosome without affecting earlier steps in endocytosis. Therefore actin is a physical barrier impeding uncoated vesicle trafficking, and myo6 is recruited to move the vesicles through this barrier for fusion with the early endosome.

Indexed as

ActinsBridged Bicyclo Compounds, HeterocyclicCell LineDimethyl SulfoxideEndocytosisEndosomesGreen Fluorescent ProteinsHumansMicroscopy, FluorescenceMyosin Heavy ChainsProtein TransportThiazolesThiazolidinesTransferrinTransport VesiclesActinsBridged Bicyclo Compounds, HeterocyclicDimethyl Sulfoxideenhanced green fluorescent proteinGreen Fluorescent Proteinslatrunculin AMyosin Heavy Chainsmyosin VIThiazolesThiazolidinesTransferrin

Identifiers

PMID15004223
PMCPMC404020
OpenAlexW2151665709

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.