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Dedifferentiation of committed epithelial cells into stem cells in vivo

Author

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  • Purushothama Rao Tata

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Hongmei Mou

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Ana Pardo-Saganta

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Rui Zhao

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Mythili Prabhu

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Brandon M. Law

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Vladimir Vinarsky

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

  • Josalyn L. Cho

    (Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital)

  • Sylvie Breton

    (Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School)

  • Amar Sahay

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Harvard Stem Cell Institute
    Harvard Medical School)

  • Benjamin D. Medoff

    (Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital)

  • Jayaraj Rajagopal

    (Center for Regenerative Medicine, Massachusetts General Hospital, 185 Cambridge Street, Boston, Massachusetts 02114, USA
    Massachusetts General Hospital
    Pulmonary and Critical Care Unit, Massachusetts General Hospital
    Harvard Stem Cell Institute)

Abstract

Cellular plasticity contributes to the regenerative capacity of plants, invertebrates, teleost fishes and amphibians. In vertebrates, differentiated cells are known to revert into replicating progenitors, but these cells do not persist as stable stem cells. Here we present evidence that differentiated airway epithelial cells can revert into stable and functional stem cells in vivo. After the ablation of airway stem cells, we observed a surprising increase in the proliferation of committed secretory cells. Subsequent lineage tracing demonstrated that the luminal secretory cells had dedifferentiated into basal stem cells. Dedifferentiated cells were morphologically indistinguishable from stem cells and they functioned as well as their endogenous counterparts in repairing epithelial injury. Single secretory cells clonally dedifferentiated into multipotent stem cells when they were cultured ex vivo without basal stem cells. By contrast, direct contact with a single basal stem cell was sufficient to prevent secretory cell dedifferentiation. In analogy to classical descriptions of amphibian nuclear reprogramming, the propensity of committed cells to dedifferentiate is inversely correlated to their state of maturity. This capacity of committed cells to dedifferentiate into stem cells may have a more general role in the regeneration of many tissues and in multiple disease states, notably cancer.

Suggested Citation

  • Purushothama Rao Tata & Hongmei Mou & Ana Pardo-Saganta & Rui Zhao & Mythili Prabhu & Brandon M. Law & Vladimir Vinarsky & Josalyn L. Cho & Sylvie Breton & Amar Sahay & Benjamin D. Medoff & Jayaraj Ra, 2013. "Dedifferentiation of committed epithelial cells into stem cells in vivo," Nature, Nature, vol. 503(7475), pages 218-223, November.
  • Handle: RePEc:nat:nature:v:503:y:2013:i:7475:d:10.1038_nature12777
    DOI: 10.1038/nature12777
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    Cited by:

    1. Yuanyuan Chen & Reka Toth & Sara Chocarro & Dieter Weichenhan & Joschka Hey & Pavlo Lutsik & Stefan Sawall & Georgios T. Stathopoulos & Christoph Plass & Rocio Sotillo, 2022. "Club cells employ regeneration mechanisms during lung tumorigenesis," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Maik Pietzner & Robert Lorenz Chua & Eleanor Wheeler & Katharina Jechow & Julian D. S. Willett & Helena Radbruch & Saskia Trump & Bettina Heidecker & Hugo Zeberg & Frank L. Heppner & Roland Eils & Mar, 2022. "ELF5 is a potential respiratory epithelial cell-specific risk gene for severe COVID-19," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    3. Andrew K. Beppu & Juanjuan Zhao & Changfu Yao & Gianni Carraro & Edo Israely & Anna Lucia Coelho & Katherine Drake & Cory M. Hogaboam & William C. Parks & Jay K. Kolls & Barry R. Stripp, 2023. "Epithelial plasticity and innate immune activation promote lung tissue remodeling following respiratory viral infection," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    4. Zhoufeng Wang & Zhe Li & Kun Zhou & Chengdi Wang & Lili Jiang & Li Zhang & Ying Yang & Wenxin Luo & Wenliang Qiao & Gang Wang & Yinyun Ni & Shuiping Dai & Tingting Guo & Guiyi Ji & Minjie Xu & Yiying , 2021. "Deciphering cell lineage specification of human lung adenocarcinoma with single-cell RNA sequencing," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    5. Yan, Kexun & Wang, Maoxiang & Hu, Fenglan & Xu, Meng, 2023. "Effect of cellular dedifferentiation on the growth of cell lineages," Physica A: Statistical Mechanics and its Applications, Elsevier, vol. 632(P1).
    6. Wei Gu & Xiaofeng Huang & Pratik N. P. Singh & Sanlan Li & Ying Lan & Min Deng & Lauretta A. Lacko & Jesus M. Gomez-Salinero & Shahin Rafii & Michael P. Verzi & Ramesh A. Shivdasani & Qiao Zhou, 2024. "A MTA2-SATB2 chromatin complex restrains colonic plasticity toward small intestine by retaining HNF4A at colonic chromatin," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    7. Xingting Guo & Chenhui Wang & Yongchao Zhang & Ruxue Wei & Rongwen Xi, 2024. "Cell-fate conversion of intestinal cells in adult Drosophila midgut by depleting a single transcription factor," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    8. Katarina Kulhankova & Soumba Traore & Xue Cheng & Hadrien Benk-Fortin & Stéphanie Hallée & Mario Harvey & Joannie Roberge & Frédéric Couture & Sajeev Kohli & Thomas J. Gross & David K. Meyerholz & Gar, 2023. "Shuttle peptide delivers base editor RNPs to rhesus monkey airway epithelial cells in vivo," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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