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Adaptation to chronic ER stress enforces pancreatic ß-cell plasticity.
Chen, Chien-Wen; Guan, Bo-Jhih; Alzahrani, Mohammed R; Gao, Zhaofeng; Gao, Long; Bracey, Syrena; Wu, Jing; Mbow, Cheikh A; Jobava, Raul; Haataja, Leena; Zalavadia, Ajay H; Schaffer, Ashleigh E; Lee, Hugo; LaFramboise, Thomas; Bederman, Ilya; Arvan, Peter; Mathews, Clayton E; Gerling, Ivan C; Kaestner, Klaus H; Tirosh, Boaz; Engin, Feyza; Hatzoglou, Maria.
Afiliação
  • Chen CW; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA. cxc1036@case.edu.
  • Guan BJ; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Alzahrani MR; Department of Biochemistry, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Gao Z; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Gao L; Department of Genetics and Institute for Diabetes, Obesity and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
  • Bracey S; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Wu J; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Mbow CA; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Jobava R; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Haataja L; The Division of Metabolism, Endocrinology & Diabetes, University of Michigan Medical Center, Ann Arbor, MI, 48105, USA.
  • Zalavadia AH; Lerner Research Institute, Cleveland Clinic, 9620 Carnegie Ave N Bldg, Cleveland, OH, 44106, US.
  • Schaffer AE; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Lee H; Department of Biomolecular Chemistry, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, 53706, USA.
  • LaFramboise T; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Bederman I; Department of Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Arvan P; The Division of Metabolism, Endocrinology & Diabetes, University of Michigan Medical Center, Ann Arbor, MI, 48105, USA.
  • Mathews CE; Department of Pathology, Immunology and Laboratory Medicine, University of Florida College of Medicine, Gainesville, FL, US.
  • Gerling IC; Department of Medicine, University of Tennessee, Memphis, TN, US.
  • Kaestner KH; Department of Genetics and Institute for Diabetes, Obesity and Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
  • Tirosh B; Department of Biochemistry, Case Western Reserve University, Cleveland, OH, 44106, USA.
  • Engin F; The Institute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.
  • Hatzoglou M; Department of Biomolecular Chemistry, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI, 53706, USA. fengin@wisc.edu.
Nat Commun ; 13(1): 4621, 2022 08 08.
Article em En | MEDLINE | ID: mdl-35941159
Pancreatic ß-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 ß-cell identity is unknown. We show here under reversible, chronic stress conditions ß-cells undergo transcriptional and translational reprogramming associated with impaired expression of regulators of ß-cell function and identity. Upon recovery from stress, ß-cells regain their identity and function, indicating a high degree of adaptive plasticity. Remarkably, while ß-cells show resilience to episodic ER stress, when episodes exceed a threshold, ß-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 ß-cell adaptive exhaustion contributes to diabetes pathogenesis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Secretoras de Insulina / Plasticidade Celular Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Secretoras de Insulina / Plasticidade Celular Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos