Evidence map›Paper›PMID 33060332›Full record

ArticleScience (New York, N.Y.)2020

The nucleus acts as a ruler tailoring cell responses to spatial constraints.

A J Lomakin, C J Cattin, D Cuvelier, Z Alraies, M Molina, G P F Nader, N Srivastava, P J Sáez, J M Garcia-Arcos, I Y Zhitnyak and 11 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 341 papers.

0numbers the graph read from it
0cells of the map it votes in
341citing 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

341 citing papers in PubMed.

  1. AA and Parkinson's Disease.Reviews of physiology, biochemistry and pharmacology · 2027
    Review
  2. Physiological Significance and Functions of AA.Reviews of physiology, biochemistry and pharmacology · 2027
    Review
  3. AA in Rheumatoid Arthritis and Lupus.Reviews of physiology, biochemistry and pharmacology · 2027
    Review
  4. Article
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281 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

A J LomakinSt. Anna Children's Cancer Research Institute (CCRI), Vienna, Austria. alexis.lomakin@ccri.at alexis.lomakin@meduniwien.ac.at daniel.mueller@bsse.ethz.ch matthieu.piel@curie.fr.ORCID 0000-0002-5346-3426
C J CattinDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID 0000-0003-0508-6790
D CuvelierInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.
Z AlraiesInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.
M MolinaCentre for Stem Cells and Regenerative Medicine, School of Basic and Medical Biosciences, King's College London, London, UK.ORCID 0000-0001-7484-8918
G P F NaderInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.
N SrivastavaInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.ORCID 0000-0003-4177-6123
P J SáezInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.ORCID 0000-0003-0521-9426
J M Garcia-ArcosInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.ORCID 0000-0003-3420-6093
I Y ZhitnyakInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France.ORCID 0000-0002-6717-3745
A BhargavaInstitut Curie, PSL Research University, INSERM, U 932, Paris, France.
M K DriscollDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-7991-5614
E S WelfDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
R FiolkaDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-4636-5000
R J PetrieDepartment of Biology, Drexel University, Philadelphia, PA, USA.ORCID 0000-0001-9780-4969
N S De SilvaInstitut Curie, PSL Research University, INSERM, U 932, Paris, France.
J M González-GranadoLamImSys Lab, Departamento de Fisiología, Facultad de Medicina, Universidad Autónoma de Madrid (UAM), Madrid, Spain.ORCID 0000-0002-1177-869X
N ManelInstitut Curie, PSL Research University, INSERM, U 932, Paris, France.ORCID 0000-0002-1481-4430
A M Lennon-DuménilInstitut Curie, PSL Research University, INSERM, U 932, Paris, France.ORCID 0000-0002-8220-4482
D J MüllerDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland. alexis.lomakin@ccri.at alexis.lomakin@meduniwien.ac.at daniel.mueller@bsse.ethz.ch matthieu.piel@curie.fr.ORCID 0000-0003-3075-0665
M PielInstitut Curie, PSL Research University, CNRS, UMR 144, Paris, France. alexis.lomakin@ccri.at alexis.lomakin@meduniwien.ac.at daniel.mueller@bsse.ethz.ch matthieu.piel@curie.fr.ORCID 0000-0002-2848-177X

Funding

Transformative microscopes to image across spatiotemporal scalesR35GM133522 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Reto Paul Fiolka · 2019 to 2026
$3.1M
Physical mechanisms of 3D cell motilityR01GM126054 · NIGMS · DREXEL UNIVERSITY · PI PETRIE, RYAN · 2018 to 2022
$1.7M
Multiscale microscope for 3D cancer imaging in model organisms and organoidsR33CA235254 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI FIOLKA, RETO PAUL · 2019 to 2021
$930k
Mechanisms of melanoma migration and survival in 3D microenvironmentsK25CA204526 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI WELF, ERIK S · 2016 to 2020
$585k
Formation and function of lamellipodial morphology in 3D microenvironmentsK99GM123221 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI DRISCOLL, MEGHAN KATRIEN · 2018 to 2019
$180k
NCI NIH HHS K25 CA204526NCI NIH HHS R33 CA235254NIGMS NIH HHS K99 GM123221NIGMS NIH HHS R01 GM126054NIGMS NIH HHS R35 GM133522
6 · The paper itself

Abstract

The microscopic environment inside a metazoan organism is highly crowded. Whether individual cells can tailor their behavior to the limited space remains unclear. In this study, we found that cells measure the degree of spatial confinement by using their largest and stiffest organelle, the nucleus. Cell confinement below a resting nucleus size deforms the nucleus, which expands and stretches its envelope. This activates signaling to the actomyosin cortex via nuclear envelope stretch-sensitive proteins, up-regulating cell contractility. We established that the tailored contractile response constitutes a nuclear ruler-based signaling pathway involved in migratory cell behaviors. Cells rely on the nuclear ruler to modulate the motive force that enables their passage through restrictive pores in complex three-dimensional environments, a process relevant to cancer cell invasion, immune responses, and embryonic development.

Indexed as

Mechanotransduction, CellularActomyosinAnimalsCell MovementEmbryonic DevelopmentHeLa CellsHumansMiceMyosin Heavy ChainsNeoplasm InvasivenessNeoplasmsNuclear EnvelopeActomyosinMYH9 protein, humanMyosin Heavy Chains

Identifiers

PMID33060332
PMCPMC8059074

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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.