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Molecular profiles, sources and lineage restrictions of stem cells in an annelid regeneration model

Author

Listed:
  • Alexander W. Stockinger

    (Vienna Biocenter Campus (VBC)
    Department of Genetics and Microbiology
    University of Vienna
    a Doctoral School of the University of Vienna and the Medical University of Vienna)

  • Leonie Adelmann

    (Vienna Biocenter Campus (VBC)
    Department of Genetics and Microbiology
    University of Vienna
    a Doctoral School of the University of Vienna and the Medical University of Vienna)

  • Martin Fahrenberger

    (Vienna Biocenter Campus (VBC)
    University of Vienna
    a Doctoral School of the University of Vienna and the Medical University of Vienna
    University of Vienna and Medical University of Vienna)

  • Christine Ruta

    (Federal University of Rio de Janeiro)

  • B. Duygu Özpolat

    (Institut Jacques Monod
    Washington University in Saint Louis)

  • Nadja Milivojev

    (Vienna Biocenter Campus (VBC)
    Department of Genetics and Microbiology
    University of Vienna
    a Doctoral School of the University of Vienna and the Medical University of Vienna)

  • Guillaume Balavoine

    (Institut Jacques Monod
    Université Paris-Saclay)

  • Florian Raible

    (Vienna Biocenter Campus (VBC)
    Department of Genetics and Microbiology
    University of Vienna)

Abstract

Regeneration of missing body parts can be observed in diverse animal phyla, but it remains unclear to which extent these capacities rely on shared or divergent principles. Research into this question requires detailed knowledge about the involved molecular and cellular principles in suitable reference models. By combining single-cell RNA sequencing and mosaic transgenesis in the marine annelid Platynereis dumerilii, we map cellular profiles and lineage restrictions during posterior regeneration. Our data reveal cell-type specific injury responses, re-expression of positional identity factors, and the re-emergence of stem cell signatures in multiple cell populations. Epidermis and mesodermal coelomic tissue produce distinct putative posterior stem cells (PSCs) in the emerging blastema. A novel mosaic transgenesis strategy reveals both developmental compartments and lineage restrictions during regenerative growth. Our work supports the notion that posterior regeneration involves dedifferentiation, and reveals molecular and mechanistic parallels between annelid and vertebrate regeneration.

Suggested Citation

  • Alexander W. Stockinger & Leonie Adelmann & Martin Fahrenberger & Christine Ruta & B. Duygu Özpolat & Nadja Milivojev & Guillaume Balavoine & Florian Raible, 2024. "Molecular profiles, sources and lineage restrictions of stem cells in an annelid regeneration model," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54041-3
    DOI: 10.1038/s41467-024-54041-3
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    References listed on IDEAS

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    1. Olena Zhulyn & Hannah D. Rosenblatt & Leila Shokat & Shizhong Dai & Duygu Kuzuoglu-Öztürk & Zijian Zhang & Davide Ruggero & Kevan M. Shokat & Maria Barna, 2023. "Evolutionarily divergent mTOR remodels translatome for tissue regeneration," Nature, Nature, vol. 620(7972), pages 163-171, August.
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