Evidence map›Paper›PMID 28125933›Full record

ArticleTissue engineering. Part A2017

NANOG Restores Contractility of Mesenchymal Stem Cell-Based Senescent Microtissues.

Aref Shahini, Panagiotis Mistriotis, Mohammadnabi Asmani, Ruogang Zhao, Stelios T Andreadis

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  11. PBX1 attenuates HCell stress & chaperones · 2022
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  16. Review
  17. Restoring extracellular matrix synthesis in senescent stem cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  18. Article
  19. Article
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.

Aref Shahini1 Bioengineering Laboratory, Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York , Amherst, New York.
Panagiotis Mistriotis1 Bioengineering Laboratory, Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York , Amherst, New York.
Mohammadnabi Asmani2 Department of Biomedical Engineering, University at Buffalo, The State University of New York , Amherst, New York.
Ruogang Zhao2 Department of Biomedical Engineering, University at Buffalo, The State University of New York , Amherst, New York.
Stelios T Andreadis1 Bioengineering Laboratory, Department of Chemical and Biological Engineering, University at Buffalo, The State University of New York , Amherst, New York.
University at Buffalo, State University of New York · USBuffalo BioLabs · US

Funding

Stem Cells for Vascular Tissue EngineeringR01HL086582 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ANDREADIS, STELIOS THEOHARIS · 2008 to 2017
$3.1M
NHLBI NIH HHS R01 HL086582
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have been extensively used in the field of tissue engineering as a source of smooth muscle cells (SMCs). However, recent studies showed deficits in the contractile function of SMCs derived from senescent MSCs and there are no available strategies to restore the contractile function that is impaired due to cellular or organismal senescence. In this study, we developed a tetracycline-regulatable system and employed micropost tissue arrays to evaluate the effects of the embryonic transcription factor, NANOG, on the contractility of senescent MSCs. Using this system, we show that expression of NANOG fortified the actin cytoskeleton and restored contractile function that was impaired in senescent MSCs. NANOG increased the expression of smooth muscle α-actin (ACTA2) as well as the contractile force generated by cells in three-dimensional microtissues. Interestingly, NANOG worked together with transforming growth factor-beta1 to further enhance the contractility of senescent microtissues. The effect of NANOG on contractile function was sustained for about 10 days after termination of its expression. Our results show that NANOG could reverse the effects of stem cell senescence and restore the myogenic differentiation potential of senescent MSCs. These findings may enable development of novel strategies to restore the function of senescent cardiovascular and other SMC-containing tissues.

Indexed as

Cellular SenescenceMuscle ContractionActinsCells, CulturedGene ExpressionHumansMesenchymal Stem CellsMicrotubulesMuscle, SmoothNanog Homeobox ProteinPromoter Regions, GeneticRecombinant ProteinsTissue EngineeringACTA2 protein, humanActinsNanog Homeobox ProteinNANOG protein, humanRecombinant ProteinsACTIN cytoskeletonagingNANOGsenescencesmooth muscle contractionstem cells

Identifiers

PMID28125933
PMCPMC5467120
OpenAlexW2592685038

What OpenQuestion holds

Textmetadata
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.