Evidence map›Paper›PMID 23995291›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Human amniotic fluid stem cell differentiation along smooth muscle lineage.

Marco Ghionzoli, Andrea Repele, Laura Sartiani, Giulia Costanzi, Astrid Parenti, Valentina Spinelli, Anna L David, Massimo Garriboli, Giorgia Totonelli, Jun Tian and 7 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Human Adipose-Derived and Amniotic Fluid-Derived Stem Cells: A Preliminary In Vitro Study Comparing Myogenic Differentiation Capability.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

17 authors at 5 institutions in 4 countries.

Marco Ghionzoli2UCL Institute of Child Health and Great Ormond St. Hospital for Children, 30 Guilford St., London WC1N 1EH, UK. p.decoppi@ucl.ac.uk.
Andrea Repele
Laura Sartiani
Giulia Costanzi
Astrid Parenti
Valentina Spinelli
Anna L David
Massimo Garriboli
Giorgia Totonelli
Jun Tian
Stelios T Andreadis
Elisabetta Cerbai
Alessandro Mugelli
Antonio Messineo
Agostino Pierro
Simon Eaton
Paolo De Coppi
University of Florence · ITUniversity College London · GBGreat Ormond Street Hospital · GBUniversity at Buffalo, State University of New York · USInstitute of Child Health · IN

Funding

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

Abstract

Functional smooth muscle engineering requires isolation and expansion of smooth muscle cells (SMCs), and this process is particularly challenging for visceral smooth muscle tissue where progenitor cells have not been clearly identified. Herein we showed for the first time that efficient SMCs can be obtained from human amniotic fluid stem cells (hAFSCs). Clonal lines were generated from c-kit(+) hAFSCs. Differentiation toward SM lineage (SMhAFSCs) was obtained using a medium conditioned by PDGF-BB and TGF-β1. Molecular assays revealed higher level of α smooth muscle actin (α-SMA), desmin, calponin, and smoothelin in SMhAFSCs when compared to hAFSCs. Ultrastructural analysis demonstrated that SMhAFSCs also presented in the cytoplasm increased intermediate filaments, dense bodies, and glycogen deposits like SMCs. SMhAFSC metabolism evaluated via mass spectrometry showed higher glucose oxidation and an enhanced response to mitogenic stimuli in comparison to hAFSCs. Patch clamp of transduced hAFSCs with lentiviral vectors encoding ZsGreen under the control of the α-SMA promoter was performed demonstrating that SMhAFSCs retained a smooth muscle cell-like electrophysiological fingerprint. Eventually SMhAFSCs contractility was evident both at single cell level and on a collagen gel. In conclusion, we showed here that hAFSCs under selective culture conditions are able to give rise to functional SMCs.

Indexed as

Cell DifferentiationCell LineageActinsAction PotentialsAmniotic FluidCalcium-Binding ProteinsCalponinsCulture Media, ConditionedCytoplasmCytoskeletal ProteinsDesminFetal Stem CellsGlucoseGlycogenHumansMicrofilament ProteinsActinsCalcium-Binding ProteinsCalponinsCulture Media, ConditionedCytoskeletal ProteinsDesminGlucoseGlycogenMicrofilament ProteinsMuscle ProteinsPlatelet-Derived Growth FactorSMTN protein, humanTransforming Growth Factor betafetal cellsmultipotentmyogenicregenerative medicinetissue engineering

Identifiers

PMID23995291
PMCPMC6188351
OpenAlexW2102079751

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.