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Adaptation to chronic ER stress enforces pancreatic β-cell plasticity

Author

Listed:
  • Chien-Wen Chen

    (Case Western Reserve University)

  • Bo-Jhih Guan

    (Case Western Reserve University)

  • Mohammed R. Alzahrani

    (Case Western Reserve University)

  • Zhaofeng Gao

    (Case Western Reserve University)

  • Long Gao

    (University of Pennsylvania Perelman School of Medicine)

  • Syrena Bracey

    (Case Western Reserve University)

  • Jing Wu

    (Case Western Reserve University)

  • Cheikh A. Mbow

    (Case Western Reserve University)

  • Raul Jobava

    (Case Western Reserve University)

  • Leena Haataja

    (University of Michigan Medical Center)

  • Ajay H. Zalavadia

    (Cleveland Clinic)

  • Ashleigh E. Schaffer

    (Case Western Reserve University)

  • Hugo Lee

    (University of Wisconsin-Madison, School of Medicine and Public Health)

  • Thomas LaFramboise

    (Case Western Reserve University)

  • Ilya Bederman

    (Case Western Reserve University)

  • Peter Arvan

    (University of Michigan Medical Center)

  • Clayton E. Mathews

    (University of Florida College of Medicine)

  • Ivan C. Gerling

    (University of Tennessee)

  • Klaus H. Kaestner

    (University of Pennsylvania Perelman School of Medicine)

  • Boaz Tirosh

    (Case Western Reserve University
    The Hebrew University of Jerusalem)

  • Feyza Engin

    (University of Wisconsin-Madison, School of Medicine and Public Health
    University of Wisconsin-Madison, School of Medicine and Public Health)

  • Maria Hatzoglou

    (Case Western Reserve University)

Abstract

Pancreatic β-cells are prone to endoplasmic reticulum (ER) stress due to their role in insulin secretion. They require sustainable and efficient adaptive stress responses to cope with this stress. Whether episodes of chronic stress directly compromise β-cell identity is unknown. We show here under reversible, chronic stress conditions β-cells undergo transcriptional and translational reprogramming associated with impaired expression of regulators of β-cell function and identity. Upon recovery from stress, β-cells regain their identity and function, indicating a high degree of adaptive plasticity. Remarkably, while β-cells show resilience to episodic ER stress, when episodes exceed a threshold, β-cell identity is gradually lost. Single cell RNA-sequencing analysis of islets from type 1 diabetes patients indicates severe deregulation of the chronic stress-adaptation program and reveals novel biomarkers of diabetes progression. Our results suggest β-cell adaptive exhaustion contributes to diabetes pathogenesis.

Suggested Citation

  • Chien-Wen Chen & Bo-Jhih Guan & Mohammed R. Alzahrani & Zhaofeng Gao & Long Gao & Syrena Bracey & Jing Wu & Cheikh A. Mbow & Raul Jobava & Leena Haataja & Ajay H. Zalavadia & Ashleigh E. Schaffer & Hu, 2022. "Adaptation to chronic ER stress enforces pancreatic β-cell plasticity," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-32425-7
    DOI: 10.1038/s41467-022-32425-7
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    References listed on IDEAS

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    2. Junyue Cao & Malte Spielmann & Xiaojie Qiu & Xingfan Huang & Daniel M. Ibrahim & Andrew J. Hill & Fan Zhang & Stefan Mundlos & Lena Christiansen & Frank J. Steemers & Cole Trapnell & Jay Shendure, 2019. "The single-cell transcriptional landscape of mammalian organogenesis," Nature, Nature, vol. 566(7745), pages 496-502, February.
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