Anquetil Florence, Sabouri Somayeh, Thivolet Charles, Rodriguez-Calvo Teresa, Zapardiel-Gonzalo Jose, Amirian Natalie, Schneider Darius, Castillo Ericka, Lajevardi Yasaman, von Herrath Matthias G
Type 1 Diabetes Center, La Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
Type 1 Diabetes Center, La Jolla Institute for Allergy and Immunology, La Jolla, CA, USA; Novo Nordisk Diabetes Research & Development Center, Seattle, Washington, USA.
J Autoimmun. 2017 Jul;81:68-73. doi: 10.1016/j.jaut.2017.03.006. Epub 2017 Mar 18.
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.
白细胞介素-1β(IL-1β)已知可在体外引发β细胞功能障碍,并可能在1型糖尿病和2型糖尿病的发病机制中发挥作用。然而,几项试图阻断IL-1β功能的临床试验成效甚微。因此,我们重新研究了IL-1β在人类糖尿病和非糖尿病胰腺中的局部表达情况。我们从糖尿病胰腺器官捐赠者网络(nPOD)获取了胰腺组织切片,包括非糖尿病患者(n = 9)、非糖尿病自身抗体阳性患者(AAb +,n = 5)、1型糖尿病患者(n = 6)和2型糖尿病患者(n = 6)的捐赠者。通过原位杂交系统研究胰岛中IL-1β mRNA的存在情况,并通过间接免疫荧光研究IL-1β蛋白的情况。我们发现,在非糖尿病和糖尿病捐赠者中,胰岛内IL-1β的产生水平相当。有趣的是,IL-1β的主要来源是α细胞而非β细胞。我们的研究结果对先前文献中提出的IL-1β在糖尿病胰腺中的作用提出了质疑。此外,我们关于IL-1β定位的结果应促使人们进一步研究IL-1β在胰腺α细胞生理学中的作用。