IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v606y2022i7914d10.1038_s41586-022-04766-2.html
   My bibliography  Save this article

Generation of specialized blood vessels via lymphatic transdifferentiation

Author

Listed:
  • Rudra N. Das

    (Weizmann Institute of Science)

  • Yaara Tevet

    (Weizmann Institute of Science)

  • Stav Safriel

    (Weizmann Institute of Science)

  • Yanchao Han

    (Duke University School of Medicine
    Soochow University)

  • Noga Moshe

    (Weizmann Institute of Science)

  • Giuseppina Lambiase

    (Weizmann Institute of Science)

  • Ivan Bassi

    (Weizmann Institute of Science)

  • Julian Nicenboim

    (Weizmann Institute of Science)

  • Matthias Brückner

    (Max Plank Institute for Molecular Biomedicine)

  • Dana Hirsch

    (Weizmann Institute of Science)

  • Raya Eilam-Altstadter

    (Weizmann Institute of Science)

  • Wiebke Herzog

    (Max Plank Institute for Molecular Biomedicine
    Friedrich-Alexander Universität Erlangen-Nürnberg)

  • Roi Avraham

    (Weizmann Institute of Science)

  • Kenneth D. Poss

    (Duke University School of Medicine)

  • Karina Yaniv

    (Weizmann Institute of Science)

Abstract

The lineage and developmental trajectory of a cell are key determinants of cellular identity. In the vascular system, endothelial cells (ECs) of blood and lymphatic vessels differentiate and specialize to cater to the unique physiological demands of each organ1,2. Although lymphatic vessels were shown to derive from multiple cellular origins, lymphatic ECs (LECs) are not known to generate other cell types3,4. Here we use recurrent imaging and lineage-tracing of ECs in zebrafish anal fins, from early development to adulthood, to uncover a mechanism of specialized blood vessel formation through the transdifferentiation of LECs. Moreover, we demonstrate that deriving anal-fin vessels from lymphatic versus blood ECs results in functional differences in the adult organism, uncovering a link between cell ontogeny and functionality. We further use single-cell RNA-sequencing analysis to characterize the different cellular populations and transition states involved in the transdifferentiation process. Finally, we show that, similar to normal development, the vasculature is rederived from lymphatics during anal-fin regeneration, demonstrating that LECs in adult fish retain both potency and plasticity for generating blood ECs. Overall, our research highlights an innate mechanism of blood vessel formation through LEC transdifferentiation, and provides in vivo evidence for a link between cell ontogeny and functionality in ECs.

Suggested Citation

  • Rudra N. Das & Yaara Tevet & Stav Safriel & Yanchao Han & Noga Moshe & Giuseppina Lambiase & Ivan Bassi & Julian Nicenboim & Matthias Brückner & Dana Hirsch & Raya Eilam-Altstadter & Wiebke Herzog & R, 2022. "Generation of specialized blood vessels via lymphatic transdifferentiation," Nature, Nature, vol. 606(7914), pages 570-575, June.
  • Handle: RePEc:nat:nature:v:606:y:2022:i:7914:d:10.1038_s41586-022-04766-2
    DOI: 10.1038/s41586-022-04766-2
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41586-022-04766-2
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/s41586-022-04766-2?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Ivan Bassi & Moshe Grunspan & Gideon Hen & Kishore A. Ravichandran & Noga Moshe & Laura Gutierrez-Miranda & Stav R. Safriel & Daria Kostina & Amitay Shen & Carmen Almodovar & Karina Yaniv, 2024. "Endolysosomal dysfunction in radial glia progenitor cells leads to defective cerebral angiogenesis and compromised blood-brain barrier integrity," Nature Communications, Nature, vol. 15(1), pages 1-18, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:606:y:2022:i:7914:d:10.1038_s41586-022-04766-2. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.