Evidence map›Paper›PMID 29703977›Full record

ArticleNature communications2018

Deconvolution of subcellular protrusion heterogeneity and the underlying actin regulator dynamics from live cell imaging.

Chuangqi Wang, Hee June Choi, Sung-Jin Kim, Aesha Desai, Namgyu Lee, Dohoon Kim, Yongho Bae, Kwonmoo Lee

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Interpretable Fine-Grained Phenotypes of Subcellular Dynamics via Unsupervised Deep Learning.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  5. Article
  6. Article
  7. Unsupervised Contour Tracking of Live Cells by Mechanical and Cycle Consistency Losses.Proceedings. IEEE Computer Society Conference on Computer Vision and Pattern Recognition · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Data science in cell imaging.Journal of cell science · 2021
    Review
  14. Article
  15. Article
  16. 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

8 authors.

Chuangqi WangDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, 01609, USA.
Hee June ChoiDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, 01609, USA.
Sung-Jin KimDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, 01609, USA.
Aesha DesaiDepartment of Pathology and Anatomical Sciences, Computational Cell Biology, Anatomy and Pathology Program, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, 14203, USA.
Namgyu LeeDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, 01655, USA.
Dohoon KimDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, 01655, USA.
Yongho BaeDepartment of Pathology and Anatomical Sciences, Computational Cell Biology, Anatomy and Pathology Program, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, 14203, USA.ORCID http://orcid.org/0000-0002-1838-1652
Kwonmoo LeeDepartment of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, 01609, USA. klee@wpi.edu.ORCID http://orcid.org/0000-0001-6838-7094

Funding

Spatiotemporal Coordination of Actin Regulators and Traction Forces in Heterogeneous Cell ProtrusionsR15GM122012 · NIGMS · WORCESTER POLYTECHNIC INSTITUTE · PI LEE, KWONMOO · 2017 to 2017
$450k
NIGMS NIH HHS R15 GM122012
6 · The paper itself

Abstract

Cell protrusion is morphodynamically heterogeneous at the subcellular level. However, the mechanism of cell protrusion has been understood based on the ensemble average of actin regulator dynamics. Here, we establish a computational framework called HACKS (deconvolution of heterogeneous activity in coordination of cytoskeleton at the subcellular level) to deconvolve the subcellular heterogeneity of lamellipodial protrusion from live cell imaging. HACKS identifies distinct subcellular protrusion phenotypes based on machine-learning algorithms and reveals their underlying actin regulator dynamics at the leading edge. Using our method, we discover "accelerating protrusion", which is driven by the temporally ordered coordination of Arp2/3 and VASP activities. We validate our finding by pharmacological perturbations and further identify the fine regulation of Arp2/3 and VASP recruitment associated with accelerating protrusion. Our study suggests HACKS can identify specific subcellular protrusion phenotypes susceptible to pharmacological perturbation and reveal how actin regulator dynamics are changed by the perturbation.

Indexed as

Machine LearningModels, BiologicalActin CytoskeletonActin-Related Protein 2-3 ComplexActinsAnimalsCell Adhesion MoleculesCell LineCell Line, TumorCell MovementCluster AnalysisHumansIndolesIntravital MicroscopyMicrofilament ProteinsPhosphoproteinsActin-Related Protein 2-3 ComplexActinsCell Adhesion MoleculesCK-0944666IndolesMicrofilament ProteinsPhosphoproteinsVasodilator-Stimulated Phosphoprotein

Identifiers

PMID29703977
PMCPMC5923236

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Registered trials

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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.