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

Citation
Linnemann, A. K., et al. “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, pp. 4140-4152.
Center Indiana University
Author Amelia K Linnemann, Joseph Blumer, Michelle R Marasco, Therese J Battiola, Heidi M Umhoefer, Jee Young Han, Dudley W Lamming, Dawn Belt Davis
Keywords diabetes, islet, pancreas
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 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. 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 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.

Year of Publication
2017
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Volume
31
Issue
9
Number of Pages
4140-4152
Date Published
12/2017
ISSN Number
1530-6860
DOI
10.1096/fj.201700061RR
Alternate Journal
FASEB J.
PMID
28592636
PMCID
PMC5572685
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