Interleukin 6 protects pancreatic β cells from apoptosis by stimulation of autophagy

dc.contributor.authorLinnemann, Amelia K.
dc.contributor.authorBlumer, Joseph
dc.contributor.authorMarasco, Michelle R.
dc.contributor.authorBattiola, Therese J.
dc.contributor.authorUmhoefer, Heidi M.
dc.contributor.authorHan, Jee Young
dc.contributor.authorLamming, Dudley W.
dc.contributor.authorDavis, Dawn Belt
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2019-04-30T20:24:56Z
dc.date.available2019-04-30T20:24:56Z
dc.date.issued2017-09
dc.description.abstractIL-6 is a pleiotropic cytokine with complex roles in inflammation and metabolic disease. The role of IL-6 as a pro- or anti-inflammatory cytokine is still unclear. Within the pancreatic islet, IL-6 stimulates secretion of the prosurvival incretin hormone glucagon-like peptide 1 (GLP-1) by α cells and acts directly on β cells to stimulate insulin secretion in vitro. Uncovering physiologic mechanisms promoting β-cell survival under conditions of inflammation and stress can identify important pathways for diabetes prevention and treatment. Given the established role of GLP-1 in promoting β-cell survival, we hypothesized that IL-6 may also directly protect β cells from apoptosis. Herein, we show that IL-6 robustly activates signal transducer and activator of transcription 3 (STAT3), a transcription factor that is involved in autophagy. IL-6 stimulates LC3 conversion and autophagosome formation in cultured β cells. In vivo IL-6 infusion stimulates a robust increase in lysosomes in the pancreas that is restricted to the islet. Autophagy is critical for β-cell homeostasis, particularly under conditions of stress and increased insulin demand. The stimulation of autophagy by IL-6 is regulated via multiple complementary mechanisms including inhibition of mammalian target of rapamycin complex 1 (mTORC1) and activation of Akt, ultimately leading to increases in autophagy enzyme production. Pretreatment with IL-6 renders β cells resistant to apoptosis induced by proinflammatory cytokines, and inhibition of autophagy with chloroquine prevents the ability of IL-6 to protect from apoptosis. Importantly, we find that IL-6 can activate STAT3 and the autophagy enzyme GABARAPL1 in human islets. We also see evidence of decreased IL-6 pathway signaling in islets from donors with type 2 diabetes. On the basis of our results, we propose direct stimulation of autophagy as a novel mechanism for IL-6-mediated protection of β cells from stress-induced apoptosis.—Linnemann, A. K., Blumer, J., Marasco, M. R., Battiola, T. J., Umhoefer, H. M., Han, J. Y., Lamming, D. W., Davis, D. B. Interleukin 6 protects pancreatic β cells from apoptosis by stimulation of autophagy.en_US
dc.identifier.citationLinnemann, A. K., Blumer, J., Marasco, M. R., Battiola, T. J., Umhoefer, H. M., Han, J. Y., … Davis, D. B. (2017). Interleukin 6 protects pancreatic β cells from apoptosis by stimulation of autophagy. FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 31(9), 4140–4152. doi:10.1096/fj.201700061RRen_US
dc.identifier.urihttps://hdl.handle.net/1805/19040
dc.language.isoen_USen_US
dc.publisherFederation of American Societies for Experimental Biologyen_US
dc.relation.isversionof10.1096/fj.201700061RRen_US
dc.relation.journalFASEB journalen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectPancreasen_US
dc.subjectIsleten_US
dc.subjectDiabetesen_US
dc.titleInterleukin 6 protects pancreatic β cells from apoptosis by stimulation of autophagyen_US
dc.typeArticleen_US
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572685/en_US
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