Evidence map›Paper›PMID 34031595›Full record

ArticleNature metabolism2021

Single-cell metabolic imaging reveals a SLC2A3-dependent glycolytic burst in motile endothelial cells.

David Wu, Devin L Harrison, Teodora Szasz, Chih-Fan Yeh, Tzu-Pin Shentu, Angelo Meliton, Ru-Ting Huang, Zhengjie Zhou, Gökhan M Mutlu, Jun Huang and 1 more

Open access · greenAbstract read
In one paragraph

Article in Nature metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  9. Single-Cell Metabolic Imaging Reveals Glycogen-Driven Adaptations in Endothelial Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 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

11 authors at 2 institutions in 2 countries.

David Wu *Department of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0003-3162-3238
Devin L Harrison *Department of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.
Teodora SzaszResearch Computing Center, The University of Chicago, Chicago, IL, USA.
Chih-Fan YehDivision of Cardiology, Department of Internal Medicine and Cardiovascular Center, National Taiwan University Hospital, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-0678-2264
Tzu-Pin ShentuDepartment of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.
Angelo MelitonDepartment of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.
Ru-Ting HuangDepartment of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-8360-9994
Zhengjie ZhouDepartment of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.
Gökhan M MutluDepartment of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.
Jun HuangGraduate Program in Biophysical Sciences, The University of Chicago, Chicago, IL, USA. huangjun@uchicago.edu.ORCID http://orcid.org/0000-0003-0271-4384
Yun FangDepartment of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA. yfang1@medicine.bsd.uchicago.edu.ORCID http://orcid.org/0000-0003-4597-3095
University of Chicago · USNational Taiwan University Hospital · TW

Funding

MULTIDISCIPLINARY CARDIAC SCIENCEST32HL007381 · NHLBI · UNIVERSITY OF CHICAGO · PI JEANNE M DECARA, Yoav Gilad · 1985 to 2026
$12.5M
Role of alveolar macrophages in particulate matter-induced cardiopulmonary diseaseR01ES015024 · NIEHS · UNIVERSITY OF CHICAGO · PI MUTLU, GOKHAN M. · 2006 to 2022
$6.1M
Graduate Program in Biophysical Sciences at the University of Chicago - Renewal 0T32EB009412 · NIBIB · UNIVERSITY OF CHICAGO · PI ENGEL, GREGORY S, SOSNICK, TOBIN R · 2009 to 2023
$4.9M
Molecular mechanism of natural killer cell recognitionDP2AI144245 · NIAID · UNIVERSITY OF CHICAGO · PI HUANG, JUN · 2018 to 2022
$2.9M
Coronary artery disease locus 1p32.2 and miR92a-PPAP2B signaling in endothelial mechanobiologyR01HL136765 · NHLBI · UNIVERSITY OF CHICAGO · PI FANG, YUN · 2017 to 2021
$2.0M
Spatial Delivery of MicroRNA Inhibitor via Targeted Polyelectrolyte Complex Micelles to Treat Atherosclerosis.R01HL138223 · NHLBI · UNIVERSITY OF CHICAGO · PI FANG, YUN · 2017 to 2021
$2.0M
Recognition of cross-reactive antigens by human CD4+ T cellsR00AI106941 · NIAID · UNIVERSITY OF CHICAGO · PI HUANG, JUN · 2015 to 2016
$497k
Direct visualization of serial engagement by T cell receptorsR21AI120010 · NIAID · UNIVERSITY OF CHICAGO · PI HUANG, JUN · 2015 to 2016
$425k
Regulation of vascular metabolism in acute lung injuryR00HL145113 · NHLBI · UNIVERSITY OF CHICAGO · PI WU, DAVID D · 2021 to 2022
$341k
Regulation of vascular metabolism in acute lung injuryK99HL145113 · NHLBI · UNIVERSITY OF CHICAGO · PI WU, DAVID D · 2019 to 2020
$320k
Mechanical regulation of vascular metabolismF32HL134288 · NHLBI · UNIVERSITY OF CHICAGO · PI WU, DAVID D · 2016 to 2016
$64k
NHLBI NIH HHS F32 HL134288NHLBI NIH HHS K99 HL145113NHLBI NIH HHS R00 HL145113NHLBI NIH HHS R01 HL136765NHLBI NIH HHS R01 HL138223NHLBI NIH HHS T32 HL007381NIAID NIH HHS DP2 AI144245NIAID NIH HHS R00 AI106941NIAID NIH HHS R21 AI120010NIBIB NIH HHS T32 EB009412NIEHS NIH HHS R01 ES015024
6 · The paper itself

Abstract

Single-cell motility is spatially heterogeneous and driven by metabolic energy. Directly linking cell motility to cell metabolism is technically challenging but biologically important. Here, we use single-cell metabolic imaging to measure glycolysis in individual endothelial cells with genetically encoded biosensors capable of deciphering metabolic heterogeneity at subcellular resolution. We show that cellular glycolysis fuels endothelial activation, migration and contraction and that sites of high lactate production colocalize with active cytoskeletal remodelling within an endothelial cell. Mechanistically, RhoA induces endothelial glycolysis for the phosphorylation of cofilin and myosin light chain in order to reorganize the cytoskeleton and thus control cell motility; RhoA activation triggers a glycolytic burst through the translocation of the glucose transporter SLC2A3/GLUT3 to fuel the cellular contractile machinery, as demonstrated across multiple endothelial cell types. Our data indicate that Rho-GTPase signalling coordinates energy metabolism with cytoskeleton remodelling to regulate endothelial cell motility.

Indexed as

Energy MetabolismMolecular ImagingBiomarkersCell MovementCells, CulturedComputational BiologyCytoskeletonEndothelial CellsEndothelium, VascularGlucoseGlucose Transporter Type 3GlycolysisHumansMechanical PhenomenaModels, BiologicalrhoA GTP-Binding ProteinBiomarkersGlucoseGlucose Transporter Type 3rhoA GTP-Binding ProteinRHOA protein, human

Identifiers

PMID34031595
PMCPMC8362837
OpenAlexW3164611443

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.