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Spatiotemporal reprogramming of differentiated cells underlies regeneration and neoplasia in the intestinal epithelium

Author

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  • Tsunaki Higa

    (Medical Institute of Bioregulation, Kyushu University)

  • Yasutaka Okita

    (Medical Institute of Bioregulation, Kyushu University)

  • Akinobu Matsumoto

    (Medical Institute of Bioregulation, Kyushu University)

  • Shogo Nakayama

    (Medical Institute of Bioregulation, Kyushu University)

  • Takeru Oka

    (Medical Institute of Bioregulation, Kyushu University)

  • Osamu Sugahara

    (Medical Institute of Bioregulation, Kyushu University)

  • Daisuke Koga

    (Medical Institute of Bioregulation, Kyushu University)

  • Shoichiro Takeishi

    (Medical Institute of Bioregulation, Kyushu University
    Albert Einstein College of Medicine)

  • Hirokazu Nakatsumi

    (Medical Institute of Bioregulation, Kyushu University
    Graduate School of Pharmaceutical Sciences, Nagoya City University)

  • Naoki Hosen

    (Osaka University Graduate School of Medicine, Suita)

  • Sylvie Robine

    (UMR 144, Institut Curie, 75248 Paris Cedex 05)

  • Makoto M. Taketo

    (Graduate School of Medicine, Kyoto University)

  • Toshiro Sato

    (Keio University School of Medicine)

  • Keiichi I. Nakayama

    (Medical Institute of Bioregulation, Kyushu University)

Abstract

Although the mammalian intestinal epithelium manifests robust regenerative capacity after various cytotoxic injuries, the underlying mechanism has remained unclear. Here we identify the cyclin-dependent kinase inhibitor p57 as a specific marker for a quiescent cell population located around the +4 position of intestinal crypts. Lineage tracing reveals that the p57+ cells serve as enteroendocrine/tuft cell precursors under normal conditions but dedifferentiate and act as facultative stem cells to support regeneration after injury. Single-cell transcriptomics analysis shows that the p57+ cells undergo a dynamic reprogramming process after injury that is characterized by fetal-like conversion and metaplasia-like transformation. Population-level analysis also detects such spatiotemporal reprogramming widely in other differentiated cell types. In intestinal adenoma, p57+ cells manifest homeostatic stem cell activity, in the context of constitutively activated spatiotemporal reprogramming. Our results highlight a pronounced plasticity of the intestinal epithelium that supports maintenance of tissue integrity in normal and neoplastic contexts.

Suggested Citation

  • Tsunaki Higa & Yasutaka Okita & Akinobu Matsumoto & Shogo Nakayama & Takeru Oka & Osamu Sugahara & Daisuke Koga & Shoichiro Takeishi & Hirokazu Nakatsumi & Naoki Hosen & Sylvie Robine & Makoto M. Take, 2022. "Spatiotemporal reprogramming of differentiated cells underlies regeneration and neoplasia in the intestinal epithelium," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29165-z
    DOI: 10.1038/s41467-022-29165-z
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