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

Author:

Gancz Dana1,Raftrey Brian C23,Perlmoter Gal1ORCID,Marín-Juez Rubén4ORCID,Semo Jonathan1,Matsuoka Ryota L4ORCID,Karra Ravi56,Raviv Hila1,Moshe Noga1,Addadi Yoseph7,Golani Ofra7ORCID,Poss Kenneth D5,Red-Horse Kristy23,Stainier Didier YR4ORCID,Yaniv Karina1ORCID

Affiliation:

1. Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel

2. Department of Biology, Stanford University, Stanford, United States

3. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, United States

4. Department of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany

5. Regeneration Next, Duke University, Durham, United States

6. Department of Medicine, Duke University School of Medicine, Durham, United States

7. Department of Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel

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.

Funder

H2020 European Research Council

United States-Israel Binational Science Foundation

Minerva Foundation

H and M Kimmel Institute for Stem Cell Research, the Estate of Emile Mimran

National Institutes of Health

American Heart Association

Fondation Leducq

New York Stem Cell Foundation

Max-Planck-Gesellschaft

Deutsche Forschungsgemeinschaft

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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