Evidence map›Paper›PMID 26771193›Full record

ArticlePloS one2016

Differentiation of Human Induced-Pluripotent Stem Cells into Smooth-Muscle Cells: Two Novel Protocols.

Libang Yang, Zhaohui Geng, Thomas Nickel, Caitlin Johnson, Lin Gao, James Dutton, Cody Hou, Jianyi Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  5. Article
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  9. Article
  10. Evaluation of Antibodies for Vascular Smooth Muscle Cell Characterization.Stem cell and regenerative medicine (Wilmington, Del.) · 2024
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. SFPQ Promotes Lung Cancer MalignancyFrontiers in oncology · 2022
    Article
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

Libang YangDivision of Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Zhaohui GengStem Cell Institute, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Thomas NickelDivision of Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Caitlin JohnsonDivision of Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Lin GaoDivision of Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
James DuttonStem Cell Institute, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Cody HouDivision of Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Jianyi ZhangDivision of Cardiology, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
University of Minnesota Medical Center · USUniversity of Minnesota · USUniversity of Alabama at Birmingham · US

Funding

Midwestern Progenitor Cell ConsortiumU01HL100407 · NHLBI · UNIVERSITY OF MINNESOTA · PI GARRY, DANIEL J., KYBA, MICHAEL · 2009 to 2015
$7.8M
Endogenous and exogenous mechanisms that promote myocardial remuscularization in post infarction LV remodelingR01HL114120 · NHLBI · UNIVERSITY OF MINNESOTA · PI ZHANG, JIANYI · 2012 to 2021
$5.6M
Stem Cell Therapy for Myocardial RepairR01HL067828 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI KAUFMAN, DAN S., ZHANG, JIANYI · 2001 to 2014
$4.7M
Stem Cells For Myocardial Repair: A Large Bore Magnet StudyR01HL095077 · NHLBI · UNIVERSITY OF MINNESOTA · PI ZHANG, JIANYI · 2009 to 2017
$3.8M
NHLBI NIH HHS R01 HL067828NHLBI NIH HHS R01 HL095077NHLBI NIH HHS R01 HL114120NHLBI NIH HHS R01 HL67828NHLBI NIH HHS R01 HL95077NHLBI NIH HHS U01 HL100407NHLBI NIH HHS UO1 HL100407
6 · The paper itself

Abstract

Conventional protocols for differentiating human induced-pluripotent stem cells (hiPSCs) into smooth-muscle cells (SMCs) can be inefficient and generally fail to yield cells with a specific SMC phenotype (i.e., contractile or synthetic SMCs). Here, we present two novel hiPSC-SMC differentiation protocols that yield SMCs with predominantly contractile or synthetic phenotypes. Flow cytometry analyses of smooth-muscle actin (SMA) expression indicated that ~45% of the cells obtained with each protocol assumed an SMC phenotype, and that the populations could be purified to ~95% via metabolic selection. Assessments of cellular mRNA and/or protein levels indicated that SMA, myosin heavy chain II, collagen 1, calponin, transgelin, connexin 43, and vimentin expression in the SMCs obtained via the Contractile SMC protocol and in SMCs differentiated via a traditional protocol were similar, while SMCs produced via the Sythetic SMC protocol expressed less calponin, more collagen 1, and more connexin 43. Differences were also observed in functional assessments of the two SMC populations: the two-dimensional surface area of Contractile SMCs declined more extensively (to 12% versus 44% of original size) in response to carbachol treatment, while quantification of cell migration and proliferation were greater in Synthetic SMCs. Collectively, these data demonstrate that our novel differentiation protocols can efficiently generate SMCs from hiPSCs.

Indexed as

Calcium-Binding ProteinsCalponinsCell Culture TechniquesCell DifferentiationCollagen Type IConnexin 43HumansInduced Pluripotent Stem CellsMicrofilament ProteinsMuscle ProteinsMyocytes, Smooth MuscleMyosin Heavy ChainsVimentinCalcium-Binding ProteinsCalponinsCollagen Type IConnexin 43Microfilament ProteinsMuscle ProteinsMyosin Heavy ChainstransgelinVimentin

Identifiers

PMID26771193
PMCPMC4714916
OpenAlexW2234536314

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.