Evidence map›Paper›PMID 33875851›Full record

ArticleNature materials2021

Enhanced substrate stress relaxation promotes filopodia-mediated cell migration.

Kolade Adebowale, Ze Gong, Jay C Hou, Katrina M Wisdom, Damien Garbett, Hong-Pyo Lee, Sungmin Nam, Tobias Meyer, David J Odde, Vivek B Shenoy and 1 more

Open access · greenAbstract read
In one paragraph

Article in Nature materials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed
17.6field-weighted citation impact, top 1% 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

142 citing papers in PubMed, 250 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Traction Force Microscopy for Viscoelastic Substrates: A Semi-Analytical Method.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Tough and Rapidly Relaxing Hydrogels Via Programmable Crosslink Kinetics.Advanced materials (Deerfield Beach, Fla.) · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

82 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

11 authors at 5 institutions in 1 country.

Kolade AdebowaleDepartment of Chemical Engineering, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-8925-4888
Ze GongDepartment of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-0172-0563
Jay C HouDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.
Katrina M WisdomDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Damien GarbettDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
Hong-Pyo LeeDepartment of Mechanical Engineering, Stanford University, Stanford, CA, USA.
Sungmin NamDepartment of Mechanical Engineering, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-1016-3738
Tobias MeyerDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
David J OddeDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN, USA.ORCID http://orcid.org/0000-0001-7731-2799
Vivek B ShenoyDepartment of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-2645-1016
Ovijit ChaudhuriChemistry, Engineering, and Medicine for Human Health (ChEM-H), Stanford University, Stanford, CA, USA. chaudhuri@stanford.edu.ORCID http://orcid.org/0000-0002-9287-3401
Stanford University · USUniversity of Pennsylvania · USUniversity of Minnesota · USCornell University · USHarvard University · US

Funding

PSOC@Penn Education and OutreachU54CA193417 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2015 to 2020
$10.5M
Project 2: Cell Migration in Mechanically Complex MicroenvironmentsU54CA210190 · NCI · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW, ODDE, DAVID J. · 2016 to 2020
$10.0M
Cell Signaling and Cell DecisionsR35GM127026 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI TOBIAS MEYER · 2018 to 2026
$8.5M
Pathological consequences of altered tissue mechanics in fibrosisR01EB017753 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI JANMEY, PAUL A, SHENOY, VIVEK · 2014 to 2025
$6.3M
Research Supplement - Quantitative analyses of tumor cell extravasationU01CA202177 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2015 to 2020
$4.2M
An integrated approach to melanoma metastasis and therapy resistance: effects of age-related changes in the ECM and the biomechanics of the skinR01CA232256 · NCI · WISTAR INSTITUTE · PI CUKIERMAN, EDNA, RAJ, ARJUN · 2019 to 2023
$3.0M
Role of extracellular matrix malleability in mediating breast cancer cell invasion and migrationR37CA214136 · NCI · STANFORD UNIVERSITY · PI CHAUDHURI, OVIJIT · 2018 to 2024
$2.5M
Integration of elasticity, viscosity, and plasticity in cellular mechanosensingR01EB030876 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI SHENOY, VIVEK · 2020 to 2023
$1.3M
Stanford Chem-H Chemistry/Biology Interface Predoctoral Training ProgramT32GM120007 · NIGMS · STANFORD UNIVERSITY · PI BERTOZZI, CAROLYN · 2016 to 2020
$1.2M
Identification of mechanisms involved in coordinated group migrationF32GM116328 · NIGMS · STANFORD UNIVERSITY · PI GARBETT, DAMIEN · 2015 to 2017
$179k
NCI NIH HHS R01 CA232256NCI NIH HHS R37 CA214136NCI NIH HHS U01 CA202177NCI NIH HHS U54 CA193417NCI NIH HHS U54 CA210190NIBIB NIH HHS R01 EB017753NIBIB NIH HHS R01 EB030876NIGMS NIH HHS F32 GM116328NIGMS NIH HHS R35 GM127026NIGMS NIH HHS T32 GM120007
6 · The paper itself

Abstract

Cell migration on two-dimensional substrates is typically characterized by lamellipodia at the leading edge, mature focal adhesions and spread morphologies. These observations result from adherent cell migration studies on stiff, elastic substrates, because most cells do not migrate on soft, elastic substrates. However, many biological tissues are soft and viscoelastic, exhibiting stress relaxation over time in response to a deformation. Here, we have systematically investigated the impact of substrate stress relaxation on cell migration on soft substrates. We observed that cells migrate minimally on substrates with an elastic modulus of 2 kPa that are elastic or exhibit slow stress relaxation, but migrate robustly on 2-kPa substrates that exhibit fast stress relaxation. Strikingly, migrating cells were not spread out and did not extend lamellipodial protrusions, but were instead rounded, with filopodia protrusions extending at the leading edge, and exhibited small nascent adhesions. Computational models of cell migration based on a motor-clutch framework predict the observed impact of substrate stress relaxation on cell migration and filopodia dynamics. Our findings establish substrate stress relaxation as a key requirement for robust cell migration on soft substrates and uncover a mode of two-dimensional cell migration marked by round morphologies, filopodia protrusions and weak adhesions.

Indexed as

Cell MovementBasement MembraneBiomechanical PhenomenaCell AdhesionCell LineCell Line, TumorElasticityHumansPseudopodia

Identifiers

PMID33875851
PMCPMC8390443
OpenAlexW3152670943

What OpenQuestion holds

Textmetadata
LicenceTDM
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.