Insulin-degrading enzyme regulates insulin-directed cellular autoimmunity in murine type 1 diabetes

Front Immunol. 2024 Nov 12:15:1474453. doi: 10.3389/fimmu.2024.1474453. eCollection 2024.

Abstract

Type 1 diabetes results from the destruction of pancreatic beta cells by autoreactive T cells. As an autoantigen with extremely high expression in beta cells, insulin triggers and sustains the autoimmune CD4+ and CD8+ T cell responses and islet inflammation. We have previously shown that deficiency for insulin-degrading enzyme (IDE), a ubiquitous cytosolic protease with very high affinity for insulin, induces endoplasmic reticulum (ER) stress and proliferation in islet cells and protects non-obese diabetic mice (NOD) from diabetes. Here we wondered whether IDE deficiency affects autoreactive CD8+ T cell responses to insulin and thereby immune pathogenesis in NOD mice. We find that Ide-/- NOD harbor fewer diabetogenic T cells and reduced numbers of CD8+ T cells recognizing the dominant autoantigen insulin and islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP). Using in vitro digestions and cellular antigen presentation assays, we show that generation of the dominant insulin epitope B15-23 involves both the proteasome and IDE. IDE deficiency attenuates MHC-I presentation of the immunodominant insulin epitope by beta cells to cognate CD8+ T cells. Consequently, Ide-/- islets display reduced susceptibility to autoimmune destruction upon grafting, and to killing by insulin-specific CD8+ T cells. Moreover, Ide-/- mice are partly resistant to disease transfer by CD8+ T cells specific for insulin but not for IGRP. Thus, IDE has a dual role in beta cells, regulating ER stress and proliferation while at the same time promoting insulin-directed autoreactive CD8+ T cell responses.

Keywords: CD8+ T cell; antigen presentation; antigen processing; insulin; non-obese diabetic mouse; type 1 diabetes.

MeSH terms

  • Animals
  • Antigen Presentation / immunology
  • Autoantigens / immunology
  • Autoimmunity*
  • CD8-Positive T-Lymphocytes* / immunology
  • Diabetes Mellitus, Type 1* / immunology
  • Endoplasmic Reticulum Stress / immunology
  • Female
  • Glucose-6-Phosphatase / genetics
  • Glucose-6-Phosphatase / immunology
  • Glucose-6-Phosphatase / metabolism
  • Insulin* / metabolism
  • Insulin-Secreting Cells* / immunology
  • Insulin-Secreting Cells* / metabolism
  • Insulysin* / genetics
  • Insulysin* / immunology
  • Insulysin* / metabolism
  • Mice
  • Mice, Inbred NOD*
  • Mice, Knockout*

Substances

  • Insulysin
  • Insulin
  • Autoantigens
  • G6pc2 protein, mouse
  • Glucose-6-Phosphatase

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by Juvenile Diabetes Research Foundation 5-2006-889, Juvenile Diabetes Research Foundation 1-2008-555, Fondation pour la Recherche Médicale DEQ20130326539, Agence Nationale de la Recherche ANR-18-CE92-0008, European Foundation for the Study of Diabetes-JDRF-Lilly 2017.