Evidence map›Paper›PMID 32284989›Full record

ArticleScience advances2020

Soft extracellular matrix enhances inflammatory activation of mesenchymal stromal cells to induce monocyte production and trafficking.

Sing Wan Wong, Stephen Lenzini, Madeline H Cooper, David J Mooney, Jae-Won Shin

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
14.5field-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

76 citing papers in PubMed, 115 citations in OpenAlex.

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  20. Matrix stiffness-dependent regulation of immunomodulatory genes in human MSCs is associated with the lncRNA CYTOR.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article

16 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

5 authors at 2 institutions in 1 country.

Sing Wan WongDepartment of Pharmacology and Department of Bioengineering, University of Illinois at Chicago College of Medicine, Chicago, IL, USA.ORCID 0000-0002-7518-6474
Stephen LenziniDepartment of Pharmacology and Department of Bioengineering, University of Illinois at Chicago College of Medicine, Chicago, IL, USA.ORCID 0000-0002-2585-4817
Madeline H CooperSchool of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.ORCID 0000-0001-5698-5150
David J MooneySchool of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.ORCID 0000-0001-6299-1194
Jae-Won ShinDepartment of Pharmacology and Department of Bioengineering, University of Illinois at Chicago College of Medicine, Chicago, IL, USA.ORCID 0000-0003-4823-6373
University of Illinois Chicago · USHarvard University · US

Funding

TRAINING PROGRAM IN LUNG BIOLOGY AND PATHOBIOLOGYT32HL007829 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DOLLY MEHTA · 1995 to 2026
$15.6M
MSC Encapsulation with Thin Gel CoatingR01EB023287 · NIBIB · HARVARD UNIVERSITY · PI MOONEY, DAVID J, SCADDEN, DAVID T · 2017 to 2019
$2.0M
Encapsulation of mesenchymal stromal cells in engineered microgels for resolution of lung fibrosisR01HL141255 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2019 to 2023
$2.0M
Mechanically controlled release of hematopoietic factors from mesenchymal stromal cells for blood regenerationR00HL125884 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHIN, JAE-WON · 2016 to 2018
$747k
Mechanically controlled release of hematopoietic factors from mesenchymal stromal cells for blood regenerationK99HL125884 · NHLBI · HARVARD UNIVERSITY · PI SHIN, JAE-WON · 2015 to 2016
$176k
NHLBI NIH HHS K99 HL125884NHLBI NIH HHS R00 HL125884NHLBI NIH HHS R01 HL141255NHLBI NIH HHS T32 HL007829NIBIB NIH HHS R01 EB023287
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) modulate immune cells to ameliorate multiple inflammatory pathologies. Biophysical signals that regulate this process are poorly defined. By engineering hydrogels with tunable biophysical parameters relevant to bone marrow where MSCs naturally reside, we show that soft extracellular matrix maximizes the ability of MSCs to produce paracrine factors that have been implicated in monocyte production and chemotaxis upon inflammatory stimulation by tumor necrosis factor-α (TNFα). Soft matrix increases clustering of TNF receptors, thereby enhancing NF-κB activation and downstream gene expression. Actin polymerization and lipid rafts, but not myosin-II contractility, regulate mechanosensitive activation of MSCs by TNFα. We functionally demonstrate that human MSCs primed with TNFα in soft matrix enhance production of human monocytes in marrow of xenografted mice and increase trafficking of monocytes via CCL2. The results suggest the importance of biophysical signaling in tuning inflammatory activation of stromal cells to control the innate immune system.

Indexed as

ActinsAnimalsBiomarkersCell MovementCells, CulturedChemotaxisCytokinesExtracellular MatrixHumansInflammationInflammation MediatorsLipid MetabolismMesenchymal Stem CellsMiceMonocytesNF-kappa BActinsBiomarkersCytokinesInflammation MediatorsNF-kappa BReceptors, Tumor Necrosis FactorTumor Necrosis Factor-alpha

Identifiers

PMID32284989
PMCPMC7141831
OpenAlexW3015543639

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.