| Literature DB >> 28325643 |
Florence Anquetil1, Somayeh Sabouri1, Charles Thivolet1, Teresa Rodriguez-Calvo1, Jose Zapardiel-Gonzalo1, Natalie Amirian1, Darius Schneider1, Ericka Castillo1, Yasaman Lajevardi1, Matthias G von Herrath2.
Abstract
Interleukin-1β (IL-1β) is known to trigger beta cell dysfunction in vitro and could potentially play a role during the pathogenesis of type 1 diabetes and type 2 diabetes. However, several clinical trials attempting to block IL-1β function have had minimal success. We therefore re-investigated local expression of IL-1β in human diabetic and non-diabetic pancreata. We obtained pancreatic tissue sections from the Network for Pancreatic Organ Donors with Diabetes (nPOD) including non-diabetic (n = 9), non-diabetic auto-antibody positive (AAb+, n = 5), type 1 diabetes (n = 6), and type 2 diabetes (n = 6) donors. Islets were systematically investigated for the presence of IL-1β mRNA by in situ hybridization and IL-1β protein by indirect immunofluorescence. We found that intra-islet IL-1β was produced at comparable level in both non-diabetic and diabetic donors. Interestingly, the main source for IL-1β was alpha cells but not beta cells. Our findings call into question the role of IL-1β in the diabetic pancreas as it has been proposed in previous literature. Additionally, our results regarding the localization of IL-1β should lead to further investigation into the role of IL-1β in the physiology of pancreatic alpha cells.Entities:
Keywords: Alpha cells; Interleukin-1β; Pancreas; Type 1 diabetes
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Year: 2017 PMID: 28325643 PMCID: PMC5507672 DOI: 10.1016/j.jaut.2017.03.006
Source DB: PubMed Journal: J Autoimmun ISSN: 0896-8411 Impact factor: 7.094