Evidence map›Paper›PMID 39386729›Full record

ArticlebioRxiv : the preprint server for biology2024

Transient Notch Activation Converts Pluripotent Stem Cell-Derived Cardiomyocytes Towards a Purkinje Fiber Fate.

David M Gonzalez, Rafael Dariolli, Julia Moyett, Stephanie Song, Bhavana Shewale, Jacqueline Bliley, Daniel Clarke, Avi Ma'ayan, Stacey Rentschler, Adam Feinberg and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

David M GonzalezDepartment of Cell, Developmental, and Regenerative Biology, Mount Sinai, New York, NY 10029, USA.
Rafael DariolliDepartment of Pharmacology and Systems Biology, Mount Sinai Center for Bioinformatics, Department of Artificial Intelligence and Human Health, Mount Sinai, New York, NY 10029, USA.
Julia MoyettDuke University School of Medicine, Durham, NC 27710.
Stephanie SongDepartment of Cell, Developmental, and Regenerative Biology, Mount Sinai, New York, NY 10029, USA.
Bhavana ShewaleDepartment of Cell, Developmental, and Regenerative Biology, Mount Sinai, New York, NY 10029, USA.
Jacqueline BlileyCarnegie Mellon University, Pittsburgh, PA 15213.
Daniel ClarkeDepartment of Pharmacology and Systems Biology, Mount Sinai Center for Bioinformatics, Department of Artificial Intelligence and Human Health, Mount Sinai, New York, NY 10029, USA.
Avi Ma'ayanDepartment of Pharmacology and Systems Biology, Mount Sinai Center for Bioinformatics, Department of Artificial Intelligence and Human Health, Mount Sinai, New York, NY 10029, USA.
Stacey RentschlerWashington University School of Medicine in St. Louis, Missouri MO 63110.
Adam FeinbergCarnegie Mellon University, Pittsburgh, PA 15213.ORCID 0000-0003-3338-5456
Eric SobieDepartment of Pharmacology and Systems Biology, Mount Sinai Center for Bioinformatics, Department of Artificial Intelligence and Human Health, Mount Sinai, New York, NY 10029, USA.
Nicole C DuboisDepartment of Cell, Developmental, and Regenerative Biology, Mount Sinai, New York, NY 10029, USA.ORCID 0000-0002-8467-3004

Funding

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
Defining the spatio-temporal mechanisms of ventricular cell specification and differentiationR01HL134956 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DUBOIS, NICOLE · 2018 to 2021
$1.7M
Exploring the Role of Notch Signaling in Purkinje Fiber DevelopmentF31HL152612 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GONZALEZ , DAVID MATTHEW · 2020 to 2022
$115k
NHLBI NIH HHS F31 HL152612NHLBI NIH HHS R01 HL134956NICHD NIH HHS T32 HD075735
6 · The paper itself

Abstract

Cardiac Purkinje fibers form the most distal part of the ventricular conduction system. They coordinate contraction and play a key role in ventricular arrhythmias. While many cardiac cell types can be generated from human pluripotent stem cells, methods to generate Purkinje fiber cells remain limited, hampering our understanding of Purkinje fiber biology and conduction system defects. To identify signaling pathways involved in Purkinje fiber formation, we analyzed single cell data from murine embryonic hearts and compared Purkinje fiber cells to trabecular cardiomyocytes. This identified several genes, processes, and signaling pathways putatively involved in cardiac conduction, including Notch signaling. We next tested whether Notch activation could convert human pluripotent stem cell-derived cardiomyocytes to Purkinje fiber cells. Following Notch activation, cardiomyocytes adopted an elongated morphology and displayed altered electrophysiological properties including increases in conduction velocity, spike slope, and action potential duration, all characteristic features of Purkinje fiber cells. RNA-sequencing demonstrated that Notch-activated cardiomyocytes undergo a sequential transcriptome shift, which included upregulation of key Purkinje fiber marker genes involved in fast conduction such as

Identifiers

PMID39386729
PMCPMC11463678

What OpenQuestion holds

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Registered trials

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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.