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The protein deacetylase SIRT2 exerts metabolic control over adaptive β cell proliferation
Matthew Wortham, Bastian Ramms, Chun Zeng, Jacqueline R. Benthuysen, Somesh Sai, Dennis P. Pollow, Fenfen Liu, Michael Schlichting, Austin R. Harrington, Bradley Liu, Thazha P. Prakash, Elaine C. Pirie, Han Zhu, Siyouneh Baghdasarian, Sean T. Lee, Victor A. Ruthig, Kristen L. Wells, Johan Auwerx, Orian S. Shirihai, Maike Sander
Matthew Wortham, Bastian Ramms, Chun Zeng, Jacqueline R. Benthuysen, Somesh Sai, Dennis P. Pollow, Fenfen Liu, Michael Schlichting, Austin R. Harrington, Bradley Liu, Thazha P. Prakash, Elaine C. Pirie, Han Zhu, Siyouneh Baghdasarian, Sean T. Lee, Victor A. Ruthig, Kristen L. Wells, Johan Auwerx, Orian S. Shirihai, Maike Sander
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Research Article Endocrinology Metabolism

The protein deacetylase SIRT2 exerts metabolic control over adaptive β cell proliferation

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Abstract

Selective and controlled expansion of endogenous β cells has been pursued as a potential therapy for diabetes. Ideally, such therapies would preserve feedback control of β cell proliferation to avoid excessive β cell expansion. Here, we identified a regulator of β cell proliferation whose inactivation resulted in controlled β cell expansion: the protein deacetylase sirtuin 2 (SIRT2). Sirt2 deletion in β cells of mice increased β cell proliferation during hyperglycemia with little effect under homeostatic conditions, indicating preservation of feedback control of β cell mass. SIRT2 restrains proliferation of human islet β cells, demonstrating conserved SIRT2 function. Analysis of acetylated proteins in islets treated with a SIRT2 inhibitor revealed that SIRT2 deacetylates enzymes involved in oxidative phosphorylation, dampening the adaptive increase in oxygen consumption during hyperglycemia. At the transcriptomic level, Sirt2 inactivation has context-dependent effects on β cells, with Sirt2 controlling how β cells interpret hyperglycemia as a stress. Finally, we provide proof of principle that systemic administration of a glucagon-like peptide 1–coupled (GLP1-coupled), Sirt2-targeting antisense oligonucleotide achieves β cell Sirt2 inactivation and stimulates β cell proliferation during hyperglycemia. Overall, these studies identify a therapeutic strategy for increasing β cell mass in diabetes without circumventing feedback control of β cell proliferation. Future work should test the extent to which these findings translate to human β cells from individuals with or without diabetes.

Authors

Matthew Wortham, Bastian Ramms, Chun Zeng, Jacqueline R. Benthuysen, Somesh Sai, Dennis P. Pollow, Fenfen Liu, Michael Schlichting, Austin R. Harrington, Bradley Liu, Thazha P. Prakash, Elaine C. Pirie, Han Zhu, Siyouneh Baghdasarian, Sean T. Lee, Victor A. Ruthig, Kristen L. Wells, Johan Auwerx, Orian S. Shirihai, Maike Sander

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Figure 3

SIRT2 deacetylates metabolic enzymes and restrains islet OxPhos during hyperglycemia.

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SIRT2 deacetylates metabolic enzymes and restrains islet OxPhos during h...
(A) Schematic of proteomics experiment to identify proteins deacetylated by SIRT2 in human islets. (B) GO enrichment analysis of proteins exhibiting 1.5-fold or higher acetylation following AGK2 treatment compared with vehicle control, as detected by differential abundance following lysate enrichment using an antibody recognizing acetyl-lys. (C) Schematic of metabolic enzymes deacetylated by SIRT2. Proteins with increased acetyl-lys following AGK2 treatment are indicated with red arrows. Cytosolic reactions downstream of pyruvate are shaded. (D and E) OCR of islets from untreated (D) or S961-treated (E; as in Figure 2I) control and Sirt2Δβ mice treated sequentially with the indicated glucose concentrations (in mM), oligomycin (Oligo.), FCCP, and antimycin/rotenone (A/R). n = 5–6 pools of islets/group. The OCR was assessed using size-matched islets following 48 hours of culture in standard islet medium containing 8 mM glucose (D) or in freshly isolated islets (E). Tamoxifen-treated Sirt2+/+ Pdx1CreER and Sirt2fl/+ Pdx1CreER mice were used as controls. Data are shown as the mean ± SEM. Statistical differences were calculated using a 2-way ANOVA for each time block. **P < 0.01 for genotype.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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