SERCA2 regulates proinsulin processing and processing enzyme maturation in pancreatic beta cells

dc.contributor.authorIida, Hitoshi
dc.contributor.authorKono, Tatsuyoshi
dc.contributor.authorLee, Chih‑Chun
dc.contributor.authorKrishnan, Preethi
dc.contributor.authorArvin, Matthew C.
dc.contributor.authorWeaver, Staci A.
dc.contributor.authorJarvela, Timothy S.
dc.contributor.authorBranco, Renato C. S.
dc.contributor.authorMcLaughlin, Madeline R.
dc.contributor.authorBone, Robert N.
dc.contributor.authorTong, Xin
dc.contributor.authorArvan, Peter
dc.contributor.authorLindberg, Iris
dc.contributor.authorEvans‑Molina, Carmella
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-03-28T14:19:06Z
dc.date.available2024-03-28T14:19:06Z
dc.date.issued2023
dc.description.abstractAims/hypothesis: Increased circulating levels of incompletely processed insulin (i.e. proinsulin) are observed clinically in type 1 and type 2 diabetes. Previous studies have suggested that Ca2+ signalling within beta cells regulates insulin processing and secretion; however, the mechanisms that link impaired Ca2+ signalling with defective insulin maturation remain incompletely understood. Methods: We generated mice with beta cell-specific sarcoendoplasmic reticulum Ca2+ ATPase-2 (SERCA2) deletion (βS2KO mice) and used an INS-1 cell line model of SERCA2 deficiency. Whole-body metabolic phenotyping, Ca2+ imaging, RNA-seq and protein processing assays were used to determine how loss of SERCA2 impacts beta cell function. To test key findings in human model systems, cadaveric islets were treated with diabetogenic stressors and prohormone convertase expression patterns were characterised. Results: βS2KO mice exhibited age-dependent glucose intolerance and increased plasma and pancreatic levels of proinsulin, while endoplasmic reticulum (ER) Ca2+ levels and glucose-stimulated Ca2+ synchronicity were reduced in βS2KO islets. Islets isolated from βS2KO mice and SERCA2-deficient INS-1 cells showed decreased expression of the active forms of the proinsulin processing enzymes PC1/3 and PC2. Additionally, immunofluorescence staining revealed mis-location and abnormal accumulation of proinsulin and proPC2 in the intermediate region between the ER and the Golgi (i.e. the ERGIC) and in the cis-Golgi in beta cells of βS2KO mice. Treatment of islets from human donors without diabetes with high glucose and palmitate concentrations led to reduced expression of the active forms of the proinsulin processing enzymes, thus phenocopying the findings observed in βS2KO islets and SERCA2-deficient INS-1 cells. Similar findings were observed in wild-type mouse islets treated with brefeldin A, a compound that perturbs ER-to-Golgi trafficking. Conclusions/interpretation: Taken together, these data highlight an important link between ER Ca2+ homeostasis and proinsulin processing in beta cells. Our findings suggest a model whereby chronic ER Ca2+ depletion due to SERCA2 deficiency impairs the spatial regulation of prohormone trafficking, processing and maturation within the secretory pathway. Data availability: RNA-seq data have been deposited in the Gene Expression Omnibus (GEO; accession no.: GSE207498).
dc.eprint.versionFinal published version
dc.identifier.citationIida H, Kono T, Lee CC, et al. SERCA2 regulates proinsulin processing and processing enzyme maturation in pancreatic beta cells. Diabetologia. 2023;66(11):2042-2061. doi:10.1007/s00125-023-05979-4
dc.identifier.urihttps://hdl.handle.net/1805/39594
dc.language.isoen_US
dc.publisherSpringer
dc.relation.isversionof10.1007/s00125-023-05979-4
dc.relation.journalDiabetologia
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectBeta cell biology
dc.subjectCalcium imaging
dc.subjectCalcium signalling
dc.subjectEndoplasmic reticulum
dc.subjectInsulin secretion
dc.subjectInsulin synthesis
dc.subjectProinsulin processing
dc.subjectProtein trafficking
dc.titleSERCA2 regulates proinsulin processing and processing enzyme maturation in pancreatic beta cells
dc.typeArticle
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