Nature Communications · 2022 · 102 citations · 63 references
Life SciencesCell BiologyPhysiologyGene ExpressionTranscriptional RegulationTranscriptomicsCell Identity MaintenanceCell PlasticityDiabetes MellitusPancreatic EndocrinologyPancreatic HormonesStress-responsive Gene RegulationAdaptive PlasticityBeta Cell BiologyChronic StressIslet Cell PhysiologyPancreatic Beta-cell FunctionPhysiological Stress ResponsesSingle-cell Rna SequencingTranslational Reprogramming
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.
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