4.8 Article

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

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ELIFE
卷 8, 期 -, 页码 -

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ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.44153

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  1. H2020 European Research Council [335605, 818858]
  2. United States-Israel Binational Science Foundation [2015289]
  3. Minerva Foundation [712610]
  4. National Institutes of Health [RO1-HL128503, R01 HL081674, R01 HL131319, R01 136182]
  5. New York Stem Cell Foundation
  6. Max-Planck-Gesellschaft
  7. Fondation Leducq
  8. American Heart Association
  9. Deutsche Forschungsgemeinschaft [394046768 - SFB 1366]
  10. European Research Council (ERC) [818858, 335605] Funding Source: European Research Council (ERC)

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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.

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