Evidence map›Paper›PMID 36347256›Full record

ArticleDevelopmental cell2022

Endocardium-to-coronary artery differentiation during heart development and regeneration involves sequential roles of Bmp2 and Cxcl12/Cxcr4.

Gaetano D'Amato, Ragini Phansalkar, Jeffrey A Naftaly, Xiaochen Fan, Zhainib A Amir, Pamela E Rios Coronado, Dale O Cowley, Kelsey E Quinn, Bikram Sharma, Kathleen M Caron and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 45 citations in OpenAlex.

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  20. Dissecting endothelial cell heterogeneity with new tools.Cell regeneration (London, England) · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 2 countries.

Gaetano D'AmatoDepartment of Biology, Stanford University, Stanford, CA, USA.
Ragini PhansalkarDepartment of Biology, Stanford University, Stanford, CA, USA; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Jeffrey A NaftalyDepartment of Biology, Stanford University, Stanford, CA, USA.
Xiaochen FanDepartment of Biology, Stanford University, Stanford, CA, USA.
Zhainib A AmirDepartment of Biology, Stanford University, Stanford, CA, USA.
Pamela E Rios CoronadoDepartment of Biology, Stanford University, Stanford, CA, USA.
Dale O CowleyAnimal Models Core, University of North Carolina, Chapel Hill, NC, USA.
Kelsey E QuinnDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Bikram SharmaDepartment of Biology, Ball State University, Muncie, IN, USA.
Kathleen M CaronDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Alessandra VigilanteCentre for Stem Cells and Regenerative Medicine & Institute for Liver Studies, King's College London, London, UK.
Kristy Red-HorseDepartment of Biology, Stanford University, Stanford, CA, USA; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA; Howard Hughes Medical Institute, Stanford, CA, USA. Electronic address: kredhors@stanford.edu.
Stanford University · USUniversity of North Carolina at Chapel Hill · USBall State University · USHoward Hughes Medical Institute · USKing's College London · GB

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Mechanotransduction and transcriptional regulation during artery developmentR01HL128503 · NHLBI · STANFORD UNIVERSITY · PI Mary Red-Horse · 2015 to 2026
$5.8M
Program in Translational and Experimental HematologyT32HL120824 · NHLBI · STANFORD UNIVERSITY · PI MAJETI, RAVINDRA · 2014 to 2023
$2.4M
NHLBI NIH HHS R01 HL128503NHLBI NIH HHS T32 HL120824NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Endocardial cells lining the heart lumen are coronary vessel progenitors during embryogenesis. Re-igniting this developmental process in adults could regenerate blood vessels lost during cardiac injury, but this requires additional knowledge of molecular mechanisms. Here, we use mouse genetics and scRNA-seq to identify regulators of endocardial angiogenesis and precisely assess the role of CXCL12/CXCR4 signaling. Time-specific lineage tracing demonstrated that endocardial cells differentiated into coronary endothelial cells primarily at mid-gestation. A new mouse line reporting CXCR4 activity-along with cell-specific gene deletions-demonstrated it was specifically required for artery morphogenesis rather than angiogenesis. Integrating scRNA-seq data of endocardial-derived coronary vessels from mid- and late-gestation identified a Bmp2-expressing transitioning population specific to mid-gestation. Bmp2 stimulated endocardial angiogenesis in vitro and in injured neonatal mouse hearts. Our data demonstrate how understanding the molecular mechanisms underlying endocardial angiogenesis can identify new potential therapeutic targets promoting revascularization of the injured heart.

Indexed as

Coronary VesselsEndocardiumAnimalsBone Morphogenetic Protein 2Cell DifferentiationChemokine CXCL12Endothelial CellsFemaleHeartMiceOrganogenesisPregnancyReceptors, CXCR4Bmp2 protein, mouseBone Morphogenetic Protein 2Chemokine CXCL12Cxcl12 protein, mouseCXCR4 protein, mouseReceptors, CXCR4BMP2 and Cxcl12/Cxc4 signalingcoronary vesselsendocardiumheart regeneration

Identifiers

PMID36347256
PMCPMC9833645
OpenAlexW4308471080

What OpenQuestion holds

Textmetadata
LicenceTDM
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.