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IL-1R signaling drives enteric glia-macrophage interactions in colorectal cancer

Author

Listed:
  • Lies van Baarle

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Veronica De Simone

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Linda Schneider

    (University Hospital Bonn, Medical Faculty)

  • Sneha Santhosh

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven
    University of Melbourne)

  • Saeed Abdurahiman

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Francesca Biscu

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven
    University of Edinburgh)

  • Reiner Schneider

    (University Hospital Bonn, Medical Faculty)

  • Lisa Zanoletti

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven
    University of Pavia)

  • Renata Siqueira de Mello

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Sara Verbandt

    (KU Leuven)

  • Zedong Hu

    (KU Leuven)

  • Michelle Stakenborg

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Bo-Jun Ke

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Nathalie Stakenborg

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Raquel Salvador Laureano

    (KU Leuven)

  • Balbina García-Reyes

    (University Hospital Bonn, Medical Faculty
    University Hospital Bonn, Medical Faculty)

  • Jonas Henn

    (University Hospital Bonn, Medical Faculty)

  • Marieta Toma

    (University Hospital Bonn, Medical Faculty)

  • Maxime Vanmechelen

    (Laboratory for Precision Cancer Medicine, KU Leuven
    Leuven Institute for Single-Cell Omics (LISCO), KU Leuven)

  • Guy Boeckxstaens

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven)

  • Frederik De Smet

    (Laboratory for Precision Cancer Medicine, KU Leuven
    Leuven Institute for Single-Cell Omics (LISCO), KU Leuven)

  • Abhishek D. Garg

    (KU Leuven)

  • Sales Ibiza

    (University of Antwerp)

  • Sabine Tejpar

    (KU Leuven)

  • Sven Wehner

    (University Hospital Bonn, Medical Faculty)

  • Gianluca Matteoli

    (Translational Research Center for Gastrointestinal Disorders (TARGID), KU Leuven
    Leuven Institute for Single-Cell Omics (LISCO), KU Leuven)

Abstract

Enteric glia have been recently recognized as key components of the colonic tumor microenvironment indicating their potential role in colorectal cancer pathogenesis. Although enteric glia modulate immune responses in other intestinal diseases, their interaction with the colorectal cancer immune cell compartment remains unclear. Through a combination of single-cell and bulk RNA-sequencing, both in murine models and patients, here we find that enteric glia acquire an immunomodulatory phenotype by bi-directional communication with tumor-infiltrating monocytes. The latter direct a reactive enteric glial cell phenotypic and functional switch via glial IL-1R signaling. In turn, tumor glia promote monocyte differentiation towards pro-tumorigenic SPP1+ tumor-associated macrophages by IL-6 release. Enteric glia cell abundancy correlates with worse disease outcomes in preclinical models and colorectal cancer patients. Thereby, our study reveals a neuroimmune interaction between enteric glia and tumor-associated macrophages in the colorectal tumor microenvironment, providing insights into colorectal cancer pathogenesis.

Suggested Citation

  • Lies van Baarle & Veronica De Simone & Linda Schneider & Sneha Santhosh & Saeed Abdurahiman & Francesca Biscu & Reiner Schneider & Lisa Zanoletti & Renata Siqueira de Mello & Sara Verbandt & Zedong Hu, 2024. "IL-1R signaling drives enteric glia-macrophage interactions in colorectal cancer," Nature Communications, Nature, vol. 15(1), pages 1-22, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-50438-2
    DOI: 10.1038/s41467-024-50438-2
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    References listed on IDEAS

    as
    1. Han Luo & Xuyang Xia & Li-Bin Huang & Hyunsu An & Minyuan Cao & Gyeong Dae Kim & Hai-Ning Chen & Wei-Han Zhang & Yang Shu & Xiangyu Kong & Zhixiang Ren & Pei-Heng Li & Yang Liu & Huairong Tang & Rongh, 2022. "Pan-cancer single-cell analysis reveals the heterogeneity and plasticity of cancer-associated fibroblasts in the tumor microenvironment," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    2. Jingjing Qi & Hongxiang Sun & Yao Zhang & Zhengting Wang & Zhenzhen Xun & Ziyi Li & Xinyu Ding & Rujuan Bao & Liwen Hong & Wenqing Jia & Fei Fang & Hongzhi Liu & Lei Chen & Jie Zhong & Duowu Zou & Lia, 2022. "Single-cell and spatial analysis reveal interaction of FAP+ fibroblasts and SPP1+ macrophages in colorectal cancer," Nature Communications, Nature, vol. 13(1), pages 1-20, December.
    3. Mirjana Efremova & Dietmar Rieder & Victoria Klepsch & Pornpimol Charoentong & Francesca Finotello & Hubert Hackl & Natascha Hermann-Kleiter & Martin Löwer & Gottfried Baier & Anne Krogsdam & Zlatko T, 2018. "Targeting immune checkpoints potentiates immunoediting and changes the dynamics of tumor evolution," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
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    5. Sales Ibiza & Bethania García-Cassani & Hélder Ribeiro & Tânia Carvalho & Luís Almeida & Rute Marques & Ana M. Misic & Casey Bartow-McKenney & Denise M. Larson & William J. Pavan & Gérard Eberl & Eliz, 2016. "Glial-cell-derived neuroregulators control type 3 innate lymphoid cells and gut defence," Nature, Nature, vol. 535(7612), pages 440-443, July.
    Full references (including those not matched with items on IDEAS)

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