Evidence map›Paper›PMID 33110128›Full record

ArticleScientific reports2020

Epithelial layer unjamming shifts energy metabolism toward glycolysis.

Stephen J DeCamp, Victor M K Tsuda, Jacopo Ferruzzi, Stephan A Koehler, John T Giblin, Darren Roblyer, Muhammad H Zaman, Scott T Weiss, Ayşe Kılıç, Margherita De Marzio and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Cell jamming transition is regulated by mitochondrial pyruvate transport and endocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

15 authors.

Stephen J DeCampDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Victor M K TsudaDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Jacopo FerruzziDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Stephan A KoehlerDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
John T GiblinDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Darren RoblyerDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Muhammad H ZamanDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Scott T WeissChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Ayşe KılıçChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Margherita De MarzioDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Chan Young ParkDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Nicolas Chiu OgassavaraDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Jennifer A MitchelDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
James P ButlerDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Jeffrey J FredbergDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA. jjf@harvard.edu.

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
Training Program in Molecular and Integrative Physiological SciencesT32HL007118 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LU, QUAN · 1985 to 2025
$14.3M
Physics of collective cellular migration in lung health and diseaseP01HL120839 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J · 2014 to 2018
$12.2M
Epithelial layer jamming in breast cancer cell migrationU01CA202123 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J · 2015 to 2019
$3.4M
Physics of bronchial epithelial unjammingR01HL148152 · NHLBI · HARVARD SCHOOL OF PUBLIC HEALTH · PI FREDBERG, JEFFREY J, PARK, JIN-AH · 2019 to 2022
$2.2M
NCATS NIH HHS UL1 TR002541NCI NIH HHS U01 CA202123NCI NIH HHS U01CA202123NHLBI NIH HHS P01 HL120839NHLBI NIH HHS P01HL120839NHLBI NIH HHS R01 HL148152NHLBI NIH HHS T32 HL007118
6 · The paper itself

Abstract

In development of an embryo, healing of a wound, or progression of a carcinoma, a requisite event is collective epithelial cellular migration. For example, cells at the advancing front of a wound edge tend to migrate collectively, elongate substantially, and exert tractions more forcefully compared with cells many ranks behind. With regards to energy metabolism, striking spatial gradients have recently been reported in the wounded epithelium, as well as in the tumor, but within the wounded cell layer little is known about the link between mechanical events and underlying energy metabolism. Using the advancing confluent monolayer of MDCKII cells as a model system, here we report at single cell resolution the evolving spatiotemporal fields of cell migration speeds, cell shapes, and traction forces measured simultaneously with fields of multiple indices of cellular energy metabolism. Compared with the epithelial layer that is unwounded, which is non-migratory, solid-like and jammed, the leading edge of the advancing cell layer is shown to become progressively more migratory, fluid-like, and unjammed. In doing so the cytoplasmic redox ratio becomes progressively smaller, the NADH lifetime becomes progressively shorter, and the mitochondrial membrane potential and glucose uptake become progressively larger. These observations indicate that a metabolic shift toward glycolysis accompanies collective cellular migration but show, further, that this shift occurs throughout the cell layer, even in regions where associated changes in cell shapes, traction forces, and migration velocities have yet to penetrate. In characterizing the wound healing process these morphological, mechanical, and metabolic observations, taken on a cell-by-cell basis, comprise the most comprehensive set of biophysical data yet reported. Together, these data suggest the novel hypothesis that the unjammed phase evolved to accommodate fluid-like migratory dynamics during episodes of tissue wound healing, development, and plasticity, but is more energetically expensive compared with the jammed phase, which evolved to maintain a solid-like non-migratory state that is more energetically economical.

Indexed as

Energy MetabolismGlycolysisAnimalsCell MovementDogsEpitheliumGlucoseMadin Darby Canine Kidney CellsMembrane Potential, MitochondrialNADOxidation-ReductionGlucoseNAD

Identifiers

PMID33110128
PMCPMC7591531

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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.