Evidence map›Paper›PMID 22325265›Full record

ArticleBiophysical journal2012

A genetic strategy for the dynamic and graded control of cell mechanics, motility, and matrix remodeling.

Joanna L MacKay, Albert J Keung, Sanjay Kumar

Abstract read
In one paragraph

Article in Biophysical journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Simultaneous and independent tuning of RhoA and Rac1 activity with orthogonally inducible promoters.Integrative biology : quantitative biosciences from nano to macro · 2014
    Article
  14. Materials as stem cell regulators.Nature materials · 2014
    Review
  15. Article
  16. Article
  17. Article
  18. Transforming potential and matrix stiffness co-regulate confinement sensitivity of tumor cell migration.Integrative biology : quantitative biosciences from nano to macro · 2013
    Article
  19. Article
  20. Cellular and Molecular Bioengineering: A Tipping Point.Cellular and molecular bioengineering · 2012
    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

3 authors at 1 institution in 1 country.

Joanna L MacKayDepartment of Chemical and Biomolecular Engineering, University of California, Berkeley, California, USA.
Albert J Keung
Sanjay Kumar
University of California, Berkeley · US

Funding

TRANS-NETWORK PROJECTSU54CA143836 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI LIPHARDT, JAN T. · 2009 to 2014
$15.1M
Cellular mechanobiology: Biophysics and therapeuticsDP2OD004213 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI KUMAR, SANJAY · 2008 to 2008
$2.3M
NCI NIH HHS 1U54CA143836NCI NIH HHS U54 CA143836NIH HHS 1DP2OD004213NIH HHS DP2 OD004213
6 · The paper itself

Abstract

Cellular mechanical properties have emerged as central regulators of many critical cell behaviors, including proliferation, motility, and differentiation. Although investigators have developed numerous techniques to influence these properties indirectly by engineering the extracellular matrix (ECM), relatively few tools are available to directly engineer the cells themselves. Here we present a genetic strategy for obtaining graded, dynamic control over cellular mechanical properties by regulating the expression of mutant mechanotransductive proteins from a single copy of a gene placed under a repressible promoter. With the use of constitutively active mutants of RhoA GTPase and myosin light chain kinase, we show that varying the expression level of either protein produces graded changes in stress fiber assembly, traction force generation, cellular stiffness, and migration speed. Using this approach, we demonstrate that soft ECMs render cells maximally sensitive to changes in RhoA activity, and that by modulating the ability of cells to engage and contract soft ECMs, we can dynamically control cell spreading, migration, and matrix remodeling. Thus, in addition to providing quantitative relationships between mechanotransductive signaling, cellular mechanical properties, and dynamic cell behaviors, this strategy enables us to control the physical interactions between cells and the ECM and thereby dictate how cells respond to matrix properties.

Indexed as

Mechanical PhenomenaBiomechanical PhenomenaCell LineCell MovementCollagenExtracellular MatrixGene Expression RegulationGenetic EngineeringHumansMechanotransduction, CellularMutationPromoter Regions, GeneticTetracyclineCollagenTetracycline

Identifiers

PMID22325265
PMCPMC3274793
OpenAlexW2132064019

What OpenQuestion holds

Textmetadata
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.