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Single-cell transcriptomics reveal the dynamic of haematopoietic stem cell production in the aorta

Author

Listed:
  • Chloé S. Baron

    (University Medical Center Utrecht)

  • Lennart Kester

    (University Medical Center Utrecht)

  • Anna Klaus

    (University Medical Center Utrecht)

  • Jean-Charles Boisset

    (University Medical Center Utrecht)

  • Roshana Thambyrajah

    (The University of Manchester)

  • Laurent Yvernogeau

    (University Medical Center Utrecht)

  • Valérie Kouskoff

    (The University of Manchester)

  • Georges Lacaud

    (The University of Manchester)

  • Alexander Oudenaarden

    (University Medical Center Utrecht)

  • Catherine Robin

    (University Medical Center Utrecht
    University Medical Center Utrecht)

Abstract

Haematopoietic stem cells (HSCs) are generated from haemogenic endothelial (HE) cells via the formation of intra-aortic haematopoietic clusters (IAHCs) in vertebrate embryos. The molecular events controlling endothelial specification, endothelial-to-haematopoietic transition (EHT) and IAHC formation, as it occurs in vivo inside the aorta, are still poorly understood. To gain insight in these processes, we performed single-cell RNA-sequencing of non-HE cells, HE cells, cells undergoing EHT, IAHC cells, and whole IAHCs isolated from mouse embryo aortas. Our analysis identified the genes and transcription factor networks activated during the endothelial-to-haematopoietic switch and IAHC cell maturation toward an HSC fate. Our study provides an unprecedented complete resource to study in depth HSC generation in vivo. It will pave the way for improving HSC production in vitro to address the growing need for tailor-made HSCs to treat patients with blood-related disorders.

Suggested Citation

  • Chloé S. Baron & Lennart Kester & Anna Klaus & Jean-Charles Boisset & Roshana Thambyrajah & Laurent Yvernogeau & Valérie Kouskoff & Georges Lacaud & Alexander Oudenaarden & Catherine Robin, 2018. "Single-cell transcriptomics reveal the dynamic of haematopoietic stem cell production in the aorta," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04893-3
    DOI: 10.1038/s41467-018-04893-3
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    Cited by:

    1. Patrick Coulombe & Grace Cole & Amanda Fentiman & Jeremy D. K. Parker & Eric Yung & Misha Bilenky & Lemlem Degefie & Patrick Lac & Maggie Y. M. Ling & Derek Tam & R. Keith Humphries & Aly Karsan, 2023. "Meis1 establishes the pre-hemogenic endothelial state prior to Runx1 expression," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    2. Brandon Hadland & Barbara Varnum-Finney & Stacey Dozono & Tessa Dignum & Cynthia Nourigat-McKay & Adam M. Heck & Takashi Ishida & Dana L. Jackson & Tomer Itkin & Jason M. Butler & Shahin Rafii & Cole , 2022. "Engineering a niche supporting hematopoietic stem cell development using integrated single-cell transcriptomics," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    3. Zaniah N. Gonzalez Galofre & Alastair M. Kilpatrick & Madalena Marques & Diana Sá da Bandeira & Telma Ventura & Mario Gomez Salazar & Léa Bouilleau & Yvan Marc & Ana B. Barbosa & Fiona Rossi & Mariana, 2024. "Runx1+ vascular smooth muscle cells are essential for hematopoietic stem and progenitor cell development in vivo," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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