Evidence map›Paper›PMID 38170020›Full record

ArticleiScience2024

Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cells.

Clifford Z Liu, Aditi Prasad, Bharati Jadhav, Yu Liu, Mingxia Gu, Andrew J Sharp, Bruce D Gelb

Open access · goldAbstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 12 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Clifford Z LiuMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Aditi PrasadMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Bharati JadhavMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Yu LiuDepartment of Medicine, Division of Cardiovascular Medicine, Stanford School of Medicine, Stanford, CA, USA.
Mingxia GuDepartment of Medicine, Division of Cardiovascular Medicine, Stanford School of Medicine, Stanford, CA, USA.
Andrew J SharpMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Bruce D GelbMindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Child Health and Development Institute · USCincinnati Children's Hospital Medical Center · USStanford Medicine · US

Funding

Pediatric Heart Disease: Getting from Mutations to TherapeuticsR35HL135742 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GELB, BRUCE D · 2017 to 2023
$6.1M
COVID and Translational Science supercomputer (CATS)S10OD030463 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2021 to 2021
$2.0M
Big Omics Data Engine 2 SupercomputerS10OD026880 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2019 to 2019
$2.0M
Interdisciplinary Training in Systems and Developmental Biology and Birth DefectsT32HD075735 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI JABS, ETHYLIN WANG · 2013 to 2022
$1.8M
NHLBI NIH HHS R35 HL135742NICHD NIH HHS T32 HD075735NIH HHS S10 OD026880NIH HHS S10 OD030463
6 · The paper itself

Abstract

Valvular heart disease presents a significant health burden, yet advancements in valve biology and therapeutics have been hindered by the lack of accessibility to human valve cells. In this study, we have developed a scalable and feeder-free method to differentiate human induced pluripotent stem cells (iPSCs) into endocardial cells, which are transcriptionally and phenotypically distinct from vascular endothelial cells. These endocardial cells can be challenged to undergo endothelial-to-mesenchymal transition (EndMT), after which two distinct populations emerge-one population undergoes EndMT to become valvular interstitial cells (VICs), while the other population reinforces their endothelial identity to become valvular endothelial cells (VECs). We then characterized these populations through bulk RNA-seq transcriptome analyses and compared our VIC and VEC populations to pseudobulk data generated from normal valve tissue of a 15-week-old human fetus. By increasing the accessibility to these cell populations, we aim to accelerate discoveries for cardiac valve biology and disease.

Indexed as

Biological sciencesCardiologyDevelopmental biologyStem cell research

Identifiers

PMID38170020
PMCPMC10758960
OpenAlexW4389210116

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.