Evidence map›Paper›PMID 27535432›Full record

ArticleMolecular biology of the cell2016

Membrane dynamics of dividing cells imaged by lattice light-sheet microscopy.

François Aguet, Srigokul Upadhyayula, Raphaël Gaudin, Yi-Ying Chou, Emanuele Cocucci, Kangmin He, Bi-Chang Chen, Kishore Mosaliganti, Mithun Pasham, Wesley Skillern and 8 more

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
27.7field-weighted citation impact, top 1% 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

82 citing papers in PubMed, 156 citations in OpenAlex.

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  9. Vesiculation pathways in clathrin-mediated endocytosis.bioRxiv : the preprint server for biology · 2025
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22 more citing papers are in PubMed but not listed here.

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

18 authors at 4 institutions in 1 country.

François AguetDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115.
Srigokul UpadhyayulaDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Raphaël GaudinDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Yi-Ying ChouDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Emanuele CocucciDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Kangmin HeDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Bi-Chang ChenJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Kishore MosaligantiDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Mithun PashamDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Wesley SkillernDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Wesley R LegantJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Tsung-Li LiuJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Greg FindlayDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Eric MarinoDepartment of Cell Biology, Harvard Medical School, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
Gaudenz DanuserLyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390.
Sean MegasonDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Eric BetzigJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
Tom KirchhausenDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115 kirchhausen@crystal.harvard.edu.
Boston Children's Hospital · USHoward Hughes Medical Institute · USHarvard University · USThe University of Texas Southwestern Medical Center · US

Funding

Request for administrative supplement to Parent R01 GM073165 entitled "Mechanisms regulating clathrin-mediated endocytosis"R01GM073165 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI METTLEN, MARCEL BERNARD · 2006 to 2022
$6.8M
Dynamics of Clathrin Coat Formation in CellsR01GM075252 · NIGMS · IMMUNE DISEASE INSTITUTE, INC. · PI KIRCHHAUSEN, TOMAS · 2005 to 2018
$4.6M
In toto Image Analysis of Tissue Mechanics during Vertebrate Ear DevelopmentK25HD071969 · NICHD · HARVARD MEDICAL SCHOOL · PI MOSALIGANTI, KISHORE RAO · 2013 to 2016
$395k
NICHD NIH HHS K25 HD071969NIGMS NIH HHS R01 GM073165NIGMS NIH HHS R01 GM075252
6 · The paper itself

Abstract

Membrane remodeling is an essential part of transferring components to and from the cell surface and membrane-bound organelles and for changes in cell shape, which are particularly critical during cell division. Earlier analyses, based on classical optical live-cell imaging and mostly restricted by technical necessity to the attached bottom surface, showed persistent formation of endocytic clathrin pits and vesicles during mitosis. Taking advantage of the resolution, speed, and noninvasive illumination of the newly developed lattice light-sheet fluorescence microscope, we reexamined their assembly dynamics over the entire cell surface and found that clathrin pits form at a lower rate during late mitosis. Full-cell imaging measurements of cell surface area and volume throughout the cell cycle of single cells in culture and in zebrafish embryos showed that the total surface increased rapidly during the transition from telophase to cytokinesis, whereas cell volume increased slightly in metaphase and was relatively constant during cytokinesis. These applications demonstrate the advantage of lattice light-sheet microscopy and enable a new standard for imaging membrane dynamics in single cells and multicellular assemblies.

Indexed as

AnimalsCell CycleCell MembraneClathrinCytokinesisEndosomesImaging, Three-DimensionalMetaphaseMicroscopyMicroscopy, FluorescenceMitosisZebrafishClathrin

Identifiers

PMID27535432
PMCPMC5221578
OpenAlexW2515641440

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.