Intra-islet insulin synthesis defects are associated with endoplasmic reticulum stress and loss of beta cell identity in human diabetes

• Published in: Diabetologia Vol. 66; no. 2; pp. 354 - 366
• Main Authors: Brusco, Noemi, Sebastiani, Guido, Di Giuseppe, Gianfranco, Licata, Giada, Grieco, Giuseppina E., Fignani, Daniela, Nigi, Laura, Formichi, Caterina, Aiello, Elena, Auddino, Stefano, Quero, Giuseppe, Cefalo, Chiara M. A., Cinti, Francesca, Mari, Andrea, Ferraro, Pietro M., Pontecorvi, Alfredo, Alfieri, Sergio, Giaccari, Andrea, Dotta, Francesco, Mezza, Teresa
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.02.2023; Springer Nature B.V
• Subjects: Beta cells; Biopsy; Cell activation; Diabetes; Diabetes mellitus (non-insulin dependent); Diabetes Mellitus, Type 2 - metabolism; Endoplasmic reticulum; Endoplasmic Reticulum Stress - genetics; Glucose - metabolism; Human Physiology; Humans; Insulin; Insulin - metabolism; Insulin secretion; Insulin-Secreting Cells - metabolism; Internal Medicine; Islets of Langerhans - metabolism; Medicine; Medicine & Public Health; Metabolic Diseases; Phenotypes; Transcription activation; Proinsulin; Type 2 diabetes; ER stress; Pancreatic islets; Dedifferentiation
• ISSN: 0012-186X; 1432-0428; 1432-0428
• DOI: 10.1007/s00125-022-05814-2

Aims/hypothesis Endoplasmic reticulum (ER) stress and beta cell dedifferentiation both play leading roles in impaired insulin secretion in overt type 2 diabetes. Whether and how these factors are related in the natural history of the disease remains, however, unclear. Methods In this study, we analysed pancreas biopsies from a cohort of metabolically characterised living donors to identify defects in in situ insulin synthesis and intra-islet expression of ER stress and beta cell phenotype markers. Results We provide evidence that in situ altered insulin processing is closely connected to in vivo worsening of beta cell function. Further, activation of ER stress genes reflects the alteration of insulin processing in situ. Using a combination of 17 different markers, we characterised individual pancreatic islets from normal glucose tolerant, impaired glucose tolerant and type 2 diabetic participants and reconstructed disease progression. Conclusions/interpretation Our study suggests that increased beta cell workload is accompanied by a progressive increase in ER stress with defects in insulin synthesis and loss of beta cell identity. Graphical abstract