Evidence map›Paper›PMID 39092506›Full record

ArticleCirculation research2024

Intramyocardial Sprouting Tip Cells Specify Coronary Arterialization.

Elena Cano, Jennifer Schwarzkopf, Masatoshi Kanda, Eric L Lindberg, Irene Hollfinger, Cristina Pogontke, Caroline Braeuning, Cornelius Fischer, Norbert Hübner, Holger Gerhardt

Abstract read
In one paragraph

Article in Circulation research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

10 authors.

Elena CanoIntegrative Vascular Biology Laboratory (E.C., J.S., I.H., H.G.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID 0000-0003-1091-8934
Jennifer SchwarzkopfIntegrative Vascular Biology Laboratory (E.C., J.S., I.H., H.G.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID 0000-0001-9552-0794
Masatoshi KandaCardiovascular and Metabolic Sciences (M.K., E.L.L., N.H.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID 0000-0003-3468-3586
Eric L LindbergCardiovascular and Metabolic Sciences (M.K., E.L.L., N.H.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID 0000-0002-2979-433X
Irene HollfingerIntegrative Vascular Biology Laboratory (E.C., J.S., I.H., H.G.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID 0000-0002-6233-8395
Cristina PogontkeDepartment of Animal Biology, University of Málaga, Spain (E.C., C.P.).ORCID 0000-0002-9610-9822
Caroline BraeuningBIH/MDC Genomics Technology Platform, Berlin, Germany (C.B., C.F.).
Cornelius FischerBIH/MDC Genomics Technology Platform, Berlin, Germany (C.B., C.F.).ORCID 0000-0003-0329-2435
Norbert HübnerCardiovascular and Metabolic Sciences (M.K., E.L.L., N.H.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Holger GerhardtIntegrative Vascular Biology Laboratory (E.C., J.S., I.H., H.G.), Max-Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe elaborate patterning of coronary arteries critically supports the high metabolic activity of the beating heart. How coronary endothelial cells coordinate hierarchical vascular remodeling and achieve arteriovenous specification remains largely unknown. Understanding the molecular and cellular cues that pattern coronary arteries is crucial to develop innovative therapeutic strategies that restore functional perfusion within the ischemic heart.

methodsSingle-cell transcriptomics and histological validation were used to delineate heterogeneous transcriptional states of the developing and mature coronary endothelium with a focus on sprouting endothelium and arterial cell specification. Genetic lineage tracing and high-resolution 3-dimensional imaging were used to characterize the origin and mechanisms of coronary angiogenic sprouting, as well as to fate-map selective endothelial lineages. Integration of single-cell transcriptomic data from ischemic adult mouse hearts and human embryonic data served to assess the conservation of transcriptional states across development, disease, and species.

resultsWe discover that coronary arteries originate from cells that have previously transitioned through a specific tip cell phenotype. We identify nonoverlapping intramyocardial and subepicardial tip cell populations with differential gene expression profiles and regulatory pathways.

conclusionsA tip cell-to-artery specification mechanism drives arterialization of the intramyocardial plexus and endocardial tunnels throughout life and is reactivated upon ischemic injury. Differential sprouting programs govern the formation and specification of the venous and arterial coronary plexus.

Indexed as

Coronary VesselsNeovascularization, PhysiologicAnimalsCell LineageEndothelial CellsFemaleHumansMaleMiceMice, Inbred C57BLMyocardiumSingle-Cell AnalysisTranscriptomeangiogenesisarteriescoronary vesselsendocardiumendothelium

Identifiers

PMID39092506
PMCPMC11361357

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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.