Evidence map›Paper›PMID 31982589›Full record

ArticleActa biomaterialia2020

Tethering transforming growth factor β1 to soft hydrogels guides vascular smooth muscle commitment from human mesenchymal stem cells.

Yonghui Ding, Richard Johnson, Sadhana Sharma, Xiaoyun Ding, Stephanie J Bryant, Wei Tan

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Yonghui DingDepartment of Mechanical Engineering, University of Colorado at Boulder, Boulder, CO 80309, United States. Electronic address: dingyonghui@connect.ust.hk.
Richard JohnsonDepartment of Mechanical Engineering, University of Colorado at Boulder, Boulder, CO 80309, United States.
Sadhana SharmaDepartment of Chemical and Biological Engineering, University of Colorado at Boulder, Boulder, CO 80309, United States.
Xiaoyun DingDepartment of Mechanical Engineering, University of Colorado at Boulder, Boulder, CO 80309, United States.
Stephanie J BryantDepartment of Chemical and Biological Engineering, University of Colorado at Boulder, Boulder, CO 80309, United States; BioFrontiers Institute, Material Science and Engineering Program, University of Colorado at Boulder, Boulder, CO 80309, United States.
Wei TanDepartment of Mechanical Engineering, University of Colorado at Boulder, Boulder, CO 80309, United States. Electronic address: wtan@colorado.edu.
University of Colorado Boulder · US

Funding

Synthetic Mesenchymal Stem Cell Niches for Vascular TherapyR01HL119371 · NHLBI · UNIVERSITY OF COLORADO · PI TAN, WEI · 2013 to 2023
$5.0M
NHLBI NIH HHS R01 HL119371
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) hold great promise for vascular smooth muscle regeneration. However, most studies have mainly relied on extended supplementation of sophisticated biochemical regimen to drive MSC differentiation towards vascular smooth muscle cells (vSMCs). Herein we demonstrate a concomitant method that exploits the advantages of biomimetic matrix stiffness and tethered transforming growth factor β1 (TGF-β1) to guide vSMC commitment from human MSCs. Our designed poly(ethylene glycol) hydrogels, presenting a biomimetic stiffness and tethered TGF-β1, provide an instructive environment to potently upregulate smooth muscle marker expression in vitro and in vivo. Importantly, it significantly enhances the functional contractility of vSMCs derived from MSCs within 3 days. Interestingly, compared to non-tethered one, tethered TGF-β1 enhanced the potency of vSMC commitment on hydrogels. We provide compelling evidence that combining stiffness and tethered TGF-β1 on poly(ethylene glycol) hydrogels can be a promising approach to drastically enhance maturation and function of vSMCs from stem cell differentiation in vitro and in vivo. STATEMENT OF SIGNIFICANCE: A fast, reliable and safe regeneration of vascular smooth muscle cells (vSMCs) from stem cell differentiation is promising for vascular tissue engineering and regenerative medicine applications, but remains challenging. Herein, a photo-click hydrogel platform is devised to recapitulate the stiffness of vascular tissue and appropriate presentation of transforming growth factor β1 (TGF-β1) to guide vSMC commitment from mesenchymal stem cells (MSCs). We demonstrate that such concomitant method drastically enhanced regeneration of mature, functional vSMCs from MSCs in vitro and in vivo within only a 3-days span. This work is not only of fundamental scientific importance, revealing how physiochemical factors and the manner of their presentation direct stem cell differentiation, but also attacks the long-standing difficulty in regenerating highly functional vSMCs within a short period.

Indexed as

Cell DifferentiationAdaptor Proteins, Signal TransducingBiomarkersFemaleHumansHydrogelsMaleMesenchymal Stem CellsMuscle ContractionMuscle, Smooth, VascularMyocytes, Smooth MuscleTranscription FactorsTransforming Growth Factor beta1Up-RegulationYAP-Signaling ProteinsYoung AdultAdaptor Proteins, Signal TransducingBiomarkersHydrogelsTranscription FactorsTransforming Growth Factor beta1YAP1 protein, humanYAP-Signaling ProteinsHydrogelsMesenchymal stem cellsSmooth muscle cellsStiffnessTransforming growth factor β1

Identifiers

PMID31982589
PMCPMC7339826
OpenAlexW3002708319

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.