Evidence map›Paper›PMID 28621931›Full record

ArticleACS applied materials & interfaces2017

Tunable Surface Repellency Maintains Stemness and Redox Capacity of Human Mesenchymal Stem Cells.

Daniel A Balikov, Spencer W Crowder, Timothy C Boire, Jung Bok Lee, Mukesh K Gupta, Aidan M Fenix, Holley N Lewis, Caitlyn M Ambrose, Philip A Short, Chang Soo Kim and 6 more

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 18 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

16 authors at 6 institutions in 3 countries.

Daniel A BalikovDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Spencer W CrowderDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Timothy C BoireDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Jung Bok LeeDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Mukesh K GuptaDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Aidan M Fenix
Holley N LewisDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Caitlyn M AmbroseDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Philip A ShortDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.
Chang Soo KimDepartment of Materials Science and Engineering, University of Wisconsin , Milwaukee, Wisconsin 53211, United States.
Dylan T Burnette
Matthew A ReillyDepartment of Biomedical Engineering, The Ohio State University , Columbus, Ohio 43210, United States.ORCID http://orcid.org/0000-0001-8029-0084
N Sanjeeva MurthyDepartment of Biomedical Engineering, Rutgers University , Piscataway, New Jersey 08854, United States.
Mi-Lan Kang
Hak-Joon SungDepartment of Biomedical Engineering, Vanderbilt University , Nashville, Tennessee 37235, United States.ORCID http://orcid.org/0000-0003-2312-2484
Vanderbilt University · USUniversity of Wisconsin–Milwaukee · USYonsei University · KRImperial College London · GBRutgers, The State University of New Jersey · USThe Ohio State University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI EMERSON, RONALD · 1986 to 2011
$28.1M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Kevin L Schey · 1989 to 2026
$19.6M
THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Overall (pp. 40-62)P41GM103485 · NIGMS · CORNELL UNIVERSITY · PI CERIONE, RICHARD A. · 2012 to 2018
$15.5M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
MOLECULAR BIOPHYSICS TRAINING PROGRAM AT VANDERBILTT32GM008320 · NIGMS · VANDERBILT UNIVERSITY · PI CHAZIN, WALTER J. · 1989 to 2023
$7.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
NCATS NIH HHS UL1 TR000445NCI NIH HHS P30 CA068485NEI NIH HHS P30 EY008126NHLBI NIH HHS F31 HL136081NIBIB NIH HHS R21 EB019509NICHD NIH HHS P30 HD015052NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U24 DK059637NIDDK NIH HHS U2C DK059637NIGMS NIH HHS P41 GM103485NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM008320
6 · The paper itself

Abstract

Human bone marrow derived mesenchymal stem cells (hMSCs) hold great promise for regenerative medicine due to their multipotent differentiation capacity and immunomodulatory capabilities. Substantial research has elucidated mechanisms by which extracellular cues regulate hMSC fate decisions, but considerably less work has addressed how material properties can be leveraged to maintain undifferentiated stem cells. Here, we show that synthetic culture substrates designed to exhibit moderate cell-repellency promote high stemness and low oxidative stress-two indicators of naïve, healthy stem cells-in commercial and patient-derived hMSCs. Furthermore, the material-mediated effect on cell behavior can be tuned by altering the molar percentage (mol %) and/or chain length of poly(ethylene glycol) (PEG), the repellant block linked to hydrophobic poly(ε-caprolactone) (PCL) in the copolymer backbone. Nano- and angstrom-scale characterization of the cell-material interface reveals that PEG interrupts the adhesive PCL domains in a chain-length-dependent manner; this prevents hMSCs from forming mature focal adhesions and subsequently promotes cell-cell adhesions that require connexin-43. This study is the first to demonstrate that intrinsic properties of synthetic materials can be tuned to regulate the stemness and redox capacity of hMSCs and provides new insight for designing highly scalable, programmable culture platforms for clinical translation.

Indexed as

Mesenchymal Stem CellsCell DifferentiationHumansOxidation-ReductionPolyethylene GlycolsRegenerative MedicinePolyethylene Glycolsbiomaterialscell-matrix interfacepolymersregenerative medicinestem cells

Identifiers

PMID28621931
PMCPMC5687519
OpenAlexW2626016153

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.