Interferon expression in the pancreases of patients with type I diabetes
- PMID: 7540571
- DOI: 10.2337/diab.44.6.658
Interferon expression in the pancreases of patients with type I diabetes
Abstract
We have used a reverse transcriptase-polymerase chain reaction (RT-PCR) protocol to examine the expression of cytokines in the pancreases and islets of patients with type I diabetes. We detect a significant increase in the level of expression of interferon (IFN)-alpha in the pancreases of the diabetic patients as compared with the control pancreases. In contrast, IFN-beta was detected at comparable levels in both groups, while IFN-gamma was detected in three of four control pancreases and one of four pancreases from the diabetic individuals. The IFN-alpha cDNAs generated by the RT-PCR were cloned and sequenced to determine which alpha-subtypes were being expressed. We found that the repertoire of subtypes was quite limited in any one individual (diabetic or not), although each individual was different with respect to the pattern of subtypes expressed. We also examined these pancreases for the expression of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-2, IL-4, and IL-6. We found no detectable expression of TNF-alpha or IL-2 in any pancreases, and the expression of the other cytokines was variable, with no pattern emerging from the comparison of the diabetic and nondiabetic individuals. We conclude that, of the cytokines examined, only IFN-alpha was significantly increased in the diabetic patients, a result that is consistent with the possibility that this cytokine is directly involved in the development of type I diabetes.
Similar articles
-
Cytokine gene expression in pancreatic islet-infiltrating leukocytes of BB rats: expression of Th1 cytokines correlates with beta-cell destructive insulitis and IDDM.Diabetes. 1996 Jun;45(6):749-54. doi: 10.2337/diab.45.6.749. Diabetes. 1996. PMID: 8635648
-
Dominant TCR alpha-chain clonotypes and interferon-gamma are expressed in the pancreas of patients with recent-onset insulin-dependent diabetes mellitus.Diabetes Res Clin Pract. 1996 Sep;34(1):37-46. doi: 10.1016/s0168-8227(96)01328-9. Diabetes Res Clin Pract. 1996. PMID: 8968689
-
Interleukin-18 mRNA, but not interleukin-18 receptor mRNA, is constitutively expressed in islet beta-cells and up-regulated by interferon-gamma.Eur Cytokine Netw. 2000 Jun;11(2):193-205. Eur Cytokine Netw. 2000. PMID: 10903798
-
Inducible nitric oxide synthase (iNOS) in pancreatic islets of nonobese diabetic mice: identification of iNOS- expressing cells and relationships to cytokines expressed in the islets.Endocrinology. 1996 May;137(5):2093-9. doi: 10.1210/endo.137.5.8612552. Endocrinology. 1996. PMID: 8612552
-
Differential regulation of Th1-type and Th2-type cytokine profiles in pancreatic islets of C57BL/6 and BALB/c mice by multiple low doses of streptozotocin.Immunobiology. 2002 Mar;205(1):35-50. doi: 10.1078/0171-2985-00109. Immunobiology. 2002. PMID: 11999343
Cited by
-
Innate Viral Sensor MDA5 and Coxsackievirus Interplay in Type 1 Diabetes Development.Microorganisms. 2020 Jul 3;8(7):993. doi: 10.3390/microorganisms8070993. Microorganisms. 2020. PMID: 32635205 Free PMC article. Review.
-
MafA Expression Preserves Immune Homeostasis in Human and Mouse Islets.Genes (Basel). 2018 Dec 18;9(12):644. doi: 10.3390/genes9120644. Genes (Basel). 2018. PMID: 30567413 Free PMC article.
-
Genetic Mechanisms Highlight Shared Pathways for the Pathogenesis of Polygenic Type 1 Diabetes and Monogenic Autoimmune Diabetes.Curr Diab Rep. 2019 Mar 19;19(5):20. doi: 10.1007/s11892-019-1141-6. Curr Diab Rep. 2019. PMID: 30888520 Free PMC article. Review.
-
Type 1 diabetes and interferon therapy: a nationwide survey in Japan.Diabetes Care. 2011 Sep;34(9):2084-9. doi: 10.2337/dc10-2274. Epub 2011 Jul 20. Diabetes Care. 2011. PMID: 21775762 Free PMC article.
-
Progression of type 1 diabetes from the prediabetic stage is controlled by interferon-α signaling.Proc Natl Acad Sci U S A. 2017 Apr 4;114(14):3708-3713. doi: 10.1073/pnas.1700878114. Epub 2017 Mar 21. Proc Natl Acad Sci U S A. 2017. PMID: 28325871 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical