Evidence map›Paper›PMID 27705776›Full record

ArticleBiophysical journal2016

A Chemomechanical Model for Nuclear Morphology and Stresses during Cell Transendothelial Migration.

Xuan Cao, Emad Moeendarbary, Philipp Isermann, Patricia M Davidson, Xiao Wang, Michelle B Chen, Anya K Burkart, Jan Lammerding, Roger D Kamm, Vivek B Shenoy

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

72 citing papers in PubMed, 140 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Micromanaging the nuclear lamina.Biophysical journal · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Mechanical signatures in cancer metastasis.npj biological physics and mechanics · 2025
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Brillouin microscopy.Nature reviews. Methods primers · 2024
    Article
  20. Article

12 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

10 authors at 3 institutions in 2 countries.

Xuan CaoDepartment of Materials Science and Engineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, Pennsylvania.
Emad MoeendarbaryDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts; Department of Mechanical Engineering, University College London, London, United Kingdom.
Philipp IsermannWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York.
Patricia M DavidsonWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York.
Xiao WangDepartment of Materials Science and Engineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, Pennsylvania.
Michelle B ChenDepartment of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Anya K BurkartDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Jan LammerdingWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York; Nancy C. and Peter E. Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York.
Roger D KammDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts; Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Vivek B ShenoyDepartment of Materials Science and Engineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, Pennsylvania. Electronic address: vshenoy@seas.upenn.edu.
Massachusetts Institute of Technology · USCornell University · USUniversity of Pennsylvania · US

Funding

TRANS-NETWORK PROJECTSU54CA143876 · NCI · CORNELL UNIVERSITY · PI SHULER, MICHAEL L · 2009 to 2014
$12.6M
PSOC@Penn Education and OutreachU54CA193417 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2015 to 2020
$10.5M
Pathological consequences of altered tissue mechanics in fibrosisR01EB017753 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI JANMEY, PAUL A, SHENOY, VIVEK · 2014 to 2025
$6.3M
Nuclear mechanics and mechanotransduction in muscular laminopathiesR01HL082792 · NHLBI · CORNELL UNIVERSITY · PI LAMMERDING, JAN · 2007 to 2023
$4.8M
Research Supplement - Quantitative analyses of tumor cell extravasationU01CA202177 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2015 to 2020
$4.2M
NCI NIH HHS U01 CA202177NCI NIH HHS U54 CA143876NCI NIH HHS U54 CA193417NHLBI NIH HHS R01 HL082792NIBIB NIH HHS R01 EB017753Wellcome Trust
6 · The paper itself

Abstract

It is now evident that the cell nucleus undergoes dramatic shape changes during important cellular processes such as cell transmigration through extracellular matrix and endothelium. Recent experimental data suggest that during cell transmigration the deformability of the nucleus could be a limiting factor, and the morphological and structural alterations that the nucleus encounters can perturb genomic organization that in turn influences cellular behavior. Despite its importance, a biophysical model that connects the experimentally observed nuclear morphological changes to the underlying biophysical factors during transmigration through small constrictions is still lacking. Here, we developed a universal chemomechanical model that describes nuclear strains and shapes and predicts thresholds for the rupture of the nuclear envelope and for nuclear plastic deformation during transmigration through small constrictions. The model includes actin contraction and cytosolic back pressure that squeeze the nucleus through constrictions and overcome the mechanical resistance from deformation of the nucleus and the constrictions. The nucleus is treated as an elastic shell encompassing a poroelastic material representing the nuclear envelope and inner nucleoplasm, respectively. Tuning the chemomechanical parameters of different components such as cell contractility and nuclear and matrix stiffnesses, our model predicts the lower bounds of constriction size for successful transmigration. Furthermore, treating the chromatin as a plastic material, our model faithfully reproduced the experimentally observed irreversible nuclear deformations after transmigration in lamin-A/C-deficient cells, whereas the wild-type cells show much less plastic deformation. Along with making testable predictions, which are in accord with our experiments and existing literature, our work provides a realistic framework to assess the biophysical modulators of nuclear deformation during cell transmigration.

Indexed as

Models, BiologicalActinsAnimalsCell NucleusCell Nucleus ShapeComputer SimulationCytosolElasticityEndothelial CellsLab-On-A-Chip DevicesMicroscopy, Atomic ForcePermeabilityPressureStress, MechanicalStress, PhysiologicalTransendothelial and Transepithelial MigrationActinsWater

Identifiers

PMID27705776
PMCPMC5052451
OpenAlexW2527731264

What OpenQuestion holds

Textmetadata
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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.