Evidence map›Paper›PMID 32328409›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2020

A Unified Linear Viscoelastic Model of the Cell Nucleus Defines the Mechanical Contributions of Lamins and Chromatin.

Oren Wintner, Nivi Hirsch-Attas, Miriam Schlossberg, Fani Brofman, Roy Friedman, Meital Kupervaser, Danny Kitsberg, Amnon Buxboim

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
6.5field-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

59 citing papers in PubMed, 106 citations in OpenAlex.

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  19. Intermediate filaments and their associated molecules.Journal of biomedical research · 2025
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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 at 3 institutions in 1 country.

Oren WintnerDepartment of Cell and Developmental Biology The Alexander Silberman Institute of Life Sciences The Hebrew University of Jerusalem Jerusalem 9190401 Israel.
Nivi Hirsch-AttasDepartment of Cell and Developmental Biology The Alexander Silberman Institute of Life Sciences The Hebrew University of Jerusalem Jerusalem 9190401 Israel.
Miriam SchlossbergDepartment of Cell and Developmental Biology The Alexander Silberman Institute of Life Sciences The Hebrew University of Jerusalem Jerusalem 9190401 Israel.
Fani BrofmanDepartment of Cell and Developmental Biology The Alexander Silberman Institute of Life Sciences The Hebrew University of Jerusalem Jerusalem 9190401 Israel.
Roy FriedmanAlexander Grass Center for Bioengineering The Rachel and Selim Benin School of Computer Science and Engineering Jerusalem 9190416 Israel.
Meital KupervaserThe de Botton Institute for Protein Profiling The Nancy and Stephen Grand Israel National Center for Personalized Medicine Weizmann Institute of Science Rehovot 7610001 Israel.
Danny KitsbergDepartment of Cell and Developmental Biology The Alexander Silberman Institute of Life Sciences The Hebrew University of Jerusalem Jerusalem 9190401 Israel.
Amnon BuxboimDepartment of Cell and Developmental Biology The Alexander Silberman Institute of Life Sciences The Hebrew University of Jerusalem Jerusalem 9190401 Israel.ORCID https://orcid.org/0000-0003-2412-9792
Hebrew University of Jerusalem · ILJerusalem Institute for Israel Studies · ILWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cell nucleus is constantly subjected to externally applied forces. During metazoan evolution, the nucleus has been optimized to allow physical deformability while protecting the genome under load. Aberrant nucleus mechanics can alter cell migration across narrow spaces in cancer metastasis and immune response and disrupt nucleus mechanosensitivity. Uncovering the mechanical roles of lamins and chromatin is imperative for understanding the implications of physiological forces on cells and nuclei. Lamin-knockout and -rescue fibroblasts and probed nucleus response to physiologically relevant stresses are generated. A minimal viscoelastic model is presented that captures dynamic resistance across different cell types, lamin composition, phosphorylation states, and chromatin condensation. The model is conserved at low and high loading and is validated by micropipette aspiration and nanoindentation rheology. A time scale emerges that separates between dominantly elastic and dominantly viscous regimes. While lamin-A and lamin-B1 contribute to nucleus stiffness, viscosity is specified mostly by lamin-A. Elastic and viscous association of lamin-B1 and lamin-A is supported by transcriptional and proteomic profiling analyses. Chromatin decondensation quantified by electron microscopy softens the nucleus unless lamin-A is expressed. A mechanical framework is provided for assessing nucleus response to applied forces in health and disease.

Indexed as

nuclear laminsnucleus mechanicsnucleus mechanobiology

Identifiers

PMID32328409
PMCPMC7175345
OpenAlexW3009348574

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.