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J Endocrinol. 2018 Aug 23. pii: JOE-18-0328. doi: 10.1530/JOE-18-0328. [Epub ahead of print]

Changes in insulin, glucagon and ER stress precede immune activation in type 1 diabetes.

Author information

1
J Crookshank, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada.
2
D Serrano, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada.
3
G Wang, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada.
4
C Patrick, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada.
5
B Morgan, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada.
6
M Pare, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada.
7
F Scott, Chronic Disease, Ottawa Hospital Research Institute, Ottawa, Canada fscott@ohri.ca.

Abstract

It is unknown whether there is a gene signature in pancreas which is associated with type 1 diabetes (T1D). We performed partial pancreatectomies on 30 day preinsulitic, diabetes-prone BioBreeding (BBdp) rats to prospectively identify factors involved in early prediabetes. Microarrays of the biopsies revealed downregulation of ER stress, metabolism and apoptosis. Based on these results, additional investigations compared gene expression in control (BBc) and BBdp rats age ~8, 30 and 60 days using RT-qPCR. Neonates had increased ER stress gene expression in pancreas. This was associated with decreased insulin, cleaved caspase-3 and Ins1 whereas Gcg and Pcsk2 were increased. The increase in ER stress was not sustained at 30 days and decreased by 60 days. In parallel, the liver gene profile showed a similar signature in neonates but with an early decrease of the unfolded protein response (UPR) at 30 days. This suggested that changes in the liver precede those in the pancreas. Tnf and Il1b expression was increased in BBdp pancreas in association with increased caspase-1, cleaved caspase-3 and decreased proinsulin area. Glucagon area was increased in both 30 day and 60 day BBdp rats. Increased co-localization of BIP and proinsulin was observed at 60 days in the pancreas, suggesting insulin-related ER dysfunction. We propose that dysregulated metabolism leads to ER stress in neonatal rats long before insulitis, creating a microenvironment in both pancreas and liver that promotes autoimmunity.

PMID:
30139929
DOI:
10.1530/JOE-18-0328

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