Evidence map›Paper›PMID 29653750›Full record

ArticleThe Journal of thoracic and cardiovascular surgery2018

Induced pluripotent stem cells with NOTCH1 gene mutation show impaired differentiation into smooth muscle and endothelial cells: Implications for bicuspid aortic valve-related aortopathy.

Jiao Jiao, Weihua Tian, Ping Qiu, Elizabeth L Norton, Michael M Wang, Y Eugene Chen, Bo Yang

Open access · greenAbstract read
In one paragraph

Article in The Journal of thoracic and cardiovascular surgery, 2018. 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
4.9field-weighted citation impact, top 4% 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, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Use of iPSC-Derived Smooth Muscle Cells to Model Physiology and Pathology.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Review
  4. Cardiac Transcription Factors and Regulatory Networks.Advances in experimental medicine and biology · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jiao JiaoDepartment of Cardiac Surgery, Michigan Medicine, Ann Arbor, Mich.
Weihua TianDepartment of Cardiac Surgery, Michigan Medicine, Ann Arbor, Mich.
Ping QiuDepartment of Cardiac Surgery, Michigan Medicine, Ann Arbor, Mich.
Elizabeth L NortonDepartment of Cardiac Surgery, Michigan Medicine, Ann Arbor, Mich.
Michael M WangDepartment of Neurology, Michigan Medicine, Ann Arbor, Mich; VA Ann Arbor Healthcare System, Ann Arbor, Mich.
Y Eugene ChenDepartment of Cardiac Surgery, Michigan Medicine, Ann Arbor, Mich.
Bo YangDepartment of Cardiac Surgery, Michigan Medicine, Ann Arbor, Mich. Electronic address: boya@med.umich.edu.
Michigan Medicine · USVA Ann Arbor Healthcare System · US

Funding

The Role of PPAR-gamma in Vascular Lesion FormationR01HL068878 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHEN, YUQING EUGENE · 2002 to 2019
$7.6M
Define the mechanisms of aortopathy in bicuspid aortic valve patientsR01HL141891 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YANG, BO · 2018 to 2022
$3.5M
Effect of mutations in the TGF-beta pathway genes on smooth muscle cell differentiation using patient derived iPSCs.K08HL130614 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YANG, BO · 2016 to 2020
$848k
NHLBI NIH HHS K08 HL130614NHLBI NIH HHS R01 HL068878NHLBI NIH HHS R01 HL141891
6 · The paper itself

Abstract

objectiveThe NOTCH1 gene mutation has been identified in bicuspid aortic valve patients. We developed an in vitro model with human induced pluripotent stem cells (iPSCs) to evaluate the role of NOTCH1 in smooth muscle and endothelial cell (EC) differentiation.

methodsThe iPSCs were derived from a patient with a normal tricuspid aortic valve and aorta. The NOTCH1 gene was targeted in iPSCs with the Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR-associated protein 9 nuclease (Cas9) system. The NOTCH1

resultsThe expression of NCSC markers (SRY-related HMG-box 10 and transcription factor AP-2 alpha) was significantly lower in NOTCH1

conclusionsNOTCH1 is critical in SMC and EC differentiation of iPSCs through NCSCs and CVPCs, respectively. NOTCH1 gene mutations might potentially contribute to the development of thoracic aortic aneurysms by affecting SMC differentiation in some patients with bicuspid aortic valve.

Indexed as

Heart Valve DiseasesReceptor, Notch1AortaAortic DiseasesAortic ValveBicuspid Aortic Valve DiseaseCell DifferentiationEndothelial CellsHumansInduced Pluripotent Stem CellsMutationMyocytes, Smooth MuscleNOTCH1 protein, humanReceptor, Notch1bicuspid aortic valveinduced pluripotent stem cellsNOTCH1smooth muscle cellsthoracic aortic aneurysm

Identifiers

PMID29653750
PMCPMC9809054
OpenAlexW2793654933

What OpenQuestion holds

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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.