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A branching model of lineage differentiation underpinning the neurogenic potential of enteric glia

Author

Listed:
  • Anna Laddach

    (the Francis Crick Institute)

  • Song Hui Chng

    (the Francis Crick Institute
    Experimental Drug Development Centre A*STAR 10 Biopolis Road)

  • Reena Lasrado

    (the Francis Crick Institute
    COMPASS Pathways PLC)

  • Fränze Progatzky

    (the Francis Crick Institute)

  • Michael Shapiro

    (the Francis Crick Institute)

  • Alek Erickson

    (Karolinska Institutet)

  • Marisol Sampedro Castaneda

    (the Francis Crick Institute)

  • Artem V. Artemov

    (Medical University of Vienna
    Boehringer Ingelheim RCV)

  • Ana Carina Bon-Frauches

    (the Francis Crick Institute)

  • Eleni-Maria Amaniti

    (the Francis Crick Institute
    Sainsbury Wellcome Centre)

  • Jens Kleinjung

    (the Francis Crick Institute
    Sosei Heptares, Steinmetz Building)

  • Stefan Boeing

    (the Francis Crick Institute)

  • Sila Ultanir

    (the Francis Crick Institute)

  • Igor Adameyko

    (Karolinska Institutet
    Medical University of Vienna)

  • Vassilis Pachnis

    (the Francis Crick Institute)

Abstract

Glial cells have been proposed as a source of neural progenitors, but the mechanisms underpinning the neurogenic potential of adult glia are not known. Using single cell transcriptomic profiling, we show that enteric glial cells represent a cell state attained by autonomic neural crest cells as they transition along a linear differentiation trajectory that allows them to retain neurogenic potential while acquiring mature glial functions. Key neurogenic loci in early enteric nervous system progenitors remain in open chromatin configuration in mature enteric glia, thus facilitating neuronal differentiation under appropriate conditions. Molecular profiling and gene targeting of enteric glial cells in a cell culture model of enteric neurogenesis and a gut injury model demonstrate that neuronal differentiation of glia is driven by transcriptional programs employed in vivo by early progenitors. Our work provides mechanistic insight into the regulatory landscape underpinning the development of intestinal neural circuits and generates a platform for advancing glial cells as therapeutic agents for the treatment of neural deficits.

Suggested Citation

  • Anna Laddach & Song Hui Chng & Reena Lasrado & Fränze Progatzky & Michael Shapiro & Alek Erickson & Marisol Sampedro Castaneda & Artem V. Artemov & Ana Carina Bon-Frauches & Eleni-Maria Amaniti & Jens, 2023. "A branching model of lineage differentiation underpinning the neurogenic potential of enteric glia," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41492-3
    DOI: 10.1038/s41467-023-41492-3
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    References listed on IDEAS

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    1. Gioele La Manno & Ruslan Soldatov & Amit Zeisel & Emelie Braun & Hannah Hochgerner & Viktor Petukhov & Katja Lidschreiber & Maria E. Kastriti & Peter Lönnerberg & Alessandro Furlan & Jean Fan & Lars E, 2018. "RNA velocity of single cells," Nature, Nature, vol. 560(7719), pages 494-498, August.
    2. Alexandre Pattyn & Xavier Morin & Harold Cremer & Christo Goridis & Jean-FranÇois Brunet, 1999. "The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives," Nature, Nature, vol. 399(6734), pages 366-370, May.
    3. Jason D. Buenrostro & Beijing Wu & Ulrike M. Litzenburger & Dave Ruff & Michael L. Gonzales & Michael P. Snyder & Howard Y. Chang & William J. Greenleaf, 2015. "Single-cell chromatin accessibility reveals principles of regulatory variation," Nature, Nature, vol. 523(7561), pages 486-490, July.
    4. Michael D Shapiro & Jessamyn Bagley & Jeff Latz & Jonathan G Godwin & Xupeng Ge & Stefan G Tullius & John Iacomini, 2011. "MicroRNA Expression Data Reveals a Signature of Kidney Damage following Ischemia Reperfusion Injury," PLOS ONE, Public Library of Science, vol. 6(8), pages 1-7, August.
    5. Hyun Ju Lee & Deniz Bartsch & Cally Xiao & Santiago Guerrero & Gaurav Ahuja & Christina Schindler & James J. Moresco & John R. Yates & Fátima Gebauer & Hisham Bazzi & Christoph Dieterich & Leo Kurian , 2017. "A post-transcriptional program coordinated by CSDE1 prevents intrinsic neural differentiation of human embryonic stem cells," Nature Communications, Nature, vol. 8(1), pages 1-19, December.
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