Evidence map›Paper›PMID 31411525›Full record

ArticleCell cycle (Georgetown, Tex.)2019

Dysfunction of iPSC-derived endothelial cells in human Hutchinson-Gilford progeria syndrome.

Gianfranco Matrone, Rajarajan A Thandavarayan, Brandon K Walther, Shu Meng, Anahita Mojiri, John P Cooke

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Guidelines for evaluating endothelial function in vascular tissue.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  3. Article
  4. Article
  5. How to measure and model cardiovascular aging.Cardiovascular research · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 1 institution in 2 countries.

Gianfranco MatroneCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute , Houston , TX , USA.ORCID https://orcid.org/0000-0001-7084-3546
Rajarajan A ThandavarayanCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute , Houston , TX , USA.
Brandon K WaltherCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute , Houston , TX , USA.
Shu MengCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute , Houston , TX , USA.ORCID https://orcid.org/0000-0002-1282-0706
Anahita MojiriCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute , Houston , TX , USA.
John P CookeCenter for Cardiovascular Regeneration, Department of Cardiovascular Sciences, Houston Methodist Research Institute , Houston , TX , USA.ORCID https://orcid.org/0000-0003-0033-9138
Houston Methodist · US

Funding

Pathological flow-induced endothelial damage and plaque erosionR01HL149303 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ABE, JUN-ICHI, COOKE, JOHN P · 2019 to 2022
$3.2M
Computational epigenetics modeling of cell identity genesR01GM125632 · NIGMS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, KAIFU · 2018 to 2021
$1.4M
NHLBI NIH HHS R01 HL149303NIGMS NIH HHS R01 GM125632
6 · The paper itself

Abstract

Children with Hutchinson-Gilford progeria syndrome (HGPS) succumb to myocardial infarction and stroke in their teen years. Endothelial dysfunction is an early event in more common forms of atherosclerosis. Endothelial pathobiology may contribute to HGPS, but a comprehensive characterization of endothelial function in HGPS has not been performed. iPSCs derived from fibroblasts of HGPS patients or unaffected relatives were differentiated into endothelial cells (ECs). Immunofluorescent signal of the pluripotent stem cell markers SSEA4, Oct4, Sox2 and TRAI-60 was similar in HGPS or control iPSCs. Following the differentiation, FACS analysis and immunocytochemistry for CD31 and CD144 revealed a smaller percentage of ECs from HGPS iPSCs. Immunostaining for Lamin A revealed nuclear dysmorphology in HGPS iPSC-ECs. Furthermore, these cells were significantly larger and rounded, and they proliferated less, features which are typical of senescent endothelial cells. HGPS iPSC-ECs manifested less Dil-Ac-LDL uptake; less DAF-2DA staining for nitric oxide generation and formed fewer networks in matrigel

Indexed as

AnimalsAntigens, CDCadherin 5CadherinsCell DifferentiationCell LineCell NucleusCell ProliferationCellular SenescenceDNA ReplicationEndothelial CellsHumansInduced Pluripotent Stem CellsLamin Type ALipoproteins, LDLMiceacetyl-LDLAntigens, CDCadherin 5CadherinsLamin Type ALipoproteins, LDLNitric OxideOctamer Transcription Factor-3PECAM1 protein, humanPlatelet Endothelial Cell Adhesion Molecule-1POU5F1 protein, humanSOX2 protein, humanSOXB1 Transcription Factorsstage-specific embryonic antigen-4Stage-Specific Embryonic Antigensdysfunctionendothelial cellsendotheliumiPSCProgeriatelomeres

Identifiers

PMID31411525
PMCPMC6738911
OpenAlexW2969034406

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.