Interleukin 6 protects pancreatic β cells from apoptosis by stimulation of autophagy
dc.contributor.author | Linnemann, Amelia K. | |
dc.contributor.author | Blumer, Joseph | |
dc.contributor.author | Marasco, Michelle R. | |
dc.contributor.author | Battiola, Therese J. | |
dc.contributor.author | Umhoefer, Heidi M. | |
dc.contributor.author | Han, Jee Young | |
dc.contributor.author | Lamming, Dudley W. | |
dc.contributor.author | Davis, Dawn Belt | |
dc.contributor.department | Pediatrics, School of Medicine | en_US |
dc.date.accessioned | 2019-04-30T20:24:56Z | |
dc.date.available | 2019-04-30T20:24:56Z | |
dc.date.issued | 2017-09 | |
dc.description.abstract | IL-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.citation | Linnemann, 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.201700061RR | en_US |
dc.identifier.uri | https://hdl.handle.net/1805/19040 | |
dc.language.iso | en_US | en_US |
dc.publisher | Federation of American Societies for Experimental Biology | en_US |
dc.relation.isversionof | 10.1096/fj.201700061RR | en_US |
dc.relation.journal | FASEB journal | en_US |
dc.rights | Publisher Policy | en_US |
dc.source | PMC | en_US |
dc.subject | Pancreas | en_US |
dc.subject | Islet | en_US |
dc.subject | Diabetes | en_US |
dc.title | Interleukin 6 protects pancreatic β cells from apoptosis by stimulation of autophagy | en_US |
dc.type | Article | en_US |
ul.alternative.fulltext | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572685/ | en_US |
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