Evidence map›Paper›PMID 31702554›Full record

ArticleeLife2019

Distinct origins and molecular mechanisms contribute to lymphatic formation during cardiac growth and regeneration.

Dana Gancz, Brian C Raftrey, Gal Perlmoter, Rubén Marín-Juez, Jonathan Semo, Ryota L Matsuoka, Ravi Karra, Hila Raviv, Noga Moshe, Yoseph Addadi and 5 more

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing 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

64 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Signal control during tissue regeneration in adult animals.Nature reviews. Molecular cell biology · 2026
    Review
  5. Emerging Light-Sheet Fluorescence Microscopy for Cardiac Vascular Imaging in Zebrafish.Current treatment options in cardiovascular medicine · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Lymphatic System Development and Function.Current cardiology reports · 2024
    Review
  15. Cardiac lymphatics undergo distinct remodeling during hypertrophic and nonhypertrophic pregnancy.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  16. Article
  17. Article
  18. Animal models to study cardiac regeneration.Nature reviews. Cardiology · 2024
    Review
  19. Review
  20. Angiogenesis-An Emerging Role in Organ Fibrosis.International journal of molecular sciences · 2023
    Review

4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Dana GanczDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Brian C Raftrey *Department of Biology, Stanford University, Stanford, United States.
Gal Perlmoter *Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-2017-3008
Rubén Marín-JuezDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0001-5903-7463
Jonathan SemoDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Ryota L MatsuokaDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0001-6214-2889
Ravi KarraRegeneration Next, Duke University, Durham, United States.
Hila RavivDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Noga MosheDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Yoseph AddadiDepartment of Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.
Ofra GolaniDepartment of Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-9793-236X
Kenneth D PossRegeneration Next, Duke University, Durham, United States.
Kristy Red-HorseDepartment of Biology, Stanford University, Stanford, United States.
Didier Yr StainierDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0002-0382-0026
Karina YanivDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-5638-7150

Funding

Regulation of Myocardial Regeneration in ZebrafishR01HL081674 · NHLBI · DUKE UNIVERSITY · PI POSS, KENNETH D · 2005 to 2019
$6.6M
Mechanotransduction and transcriptional regulation during artery developmentR01HL128503 · NHLBI · STANFORD UNIVERSITY · PI Mary Red-Horse · 2015 to 2026
$5.8M
Identification and application of regulatory elements for heart regenerationR01HL136182 · NHLBI · DUKE UNIVERSITY · PI BLACK, BRIAN L, POSS, KENNETH D · 2017 to 2020
$3.1M
Regulation of the Epicardial Injury Response During Heart Regeneration in ZebrafishR01HL131319 · NHLBI · DUKE UNIVERSITY · PI POSS, KENNETH D · 2016 to 2019
$1.6M
Deutsche Forschungsgemeinschaft 394046768 - SFB 1366H2020 European Research Council 335605H2020 European Research Council 818858Minerva Foundation 712610NHLBI NIH HHS R01 HL081674NHLBI NIH HHS R01 HL128503NHLBI NIH HHS R01 HL131319NHLBI NIH HHS R01 HL136182NIH HHS R01 136182NIH HHS R01 HL081674NIH HHS R01 HL131319NIH HHS RO1-HL128503United States-Israel Binational Science Foundation 2015289
6 · The paper itself

Abstract

In recent years, there has been increasing interest in the role of lymphatics in organ repair and regeneration, due to their importance in immune surveillance and fluid homeostasis. Experimental approaches aimed at boosting lymphangiogenesis following myocardial infarction in mice, were shown to promote healing of the heart. Yet, the mechanisms governing cardiac lymphatic growth remain unclear. Here, we identify two distinct lymphatic populations in the hearts of zebrafish and mouse, one that forms through sprouting lymphangiogenesis, and the other by coalescence of isolated lymphatic cells. By tracing the development of each subset, we reveal diverse cellular origins and differential response to signaling cues. Finally, we show that lymphatic vessels are required for cardiac regeneration in zebrafish as mutants lacking lymphatics display severely impaired regeneration capabilities. Overall, our results provide novel insight into the mechanisms underlying lymphatic formation during development and regeneration, opening new avenues for interventions targeting specific lymphatic populations.

Indexed as

AnimalsAnimals, Genetically ModifiedHeartLymphangiogenesisLymphatic SystemLymphatic VesselsMice, KnockoutMice, TransgenicMutationMyocardial InfarctionMyocardiumRegenerationSignal TransductionZebrafishcardiacdevelopmental biologylymphaticsmouseregenerationregenerative medicinestem cellszebrafish

Identifiers

PMID31702554
PMCPMC6881115

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.