The role of endoplasmic reticulum aminopeptidases in type 1 diabetes mellitus

Life Sci. 2023 Jun 15:323:121701. doi: 10.1016/j.lfs.2023.121701. Epub 2023 Apr 12.

Abstract

Type-I diabetes mellitus (T1DM) is generally considered as a chronic, T-cell mediated autoimmune disease. This notwithstanding, both the endogenous characteristics of β-cells, and their response to environmental factors and exogenous inflammatory stimuli are key events in disease progression and exacerbation. As such, T1DM is now recognized as a multifactorial condition, with its onset being influenced by both genetic predisposition and environmental factors, among which, viral infections represent major triggers. In this frame, endoplasmic reticulum aminopeptidase 1 (ERAP1) and 2 (ERAP2) hold center stage. ERAPs represent the main hydrolytic enzymes specialized in trimming of N-terminal antigen peptides to be bound by MHC class I molecules and presented to CD8+ T cells. Thus, abnormalities in ERAPs expression alter the peptide-MHC-I repertoire both quantitatively and qualitatively, fostering both autoimmune and infectious diseases. Although only a few studies succeeded in determining direct associations between ERAPs variants and T1DM susceptibility/outbreak, alterations of ERAPs do impinge on a plethora of biological events which might indeed contribute to the disease development/exacerbation. Beyond abnormal self-antigen peptide trimming, these include preproinsulin processing, nitric oxide (NO) production, ER stress, cytokine responsiveness, and immune cell recruitment/activity. The present review brings together direct and indirect evidence focused on the immunobiological role of ERAPs in T1DM onset and progression, covering both genetic and environmental aspects.

Keywords: ER stress; ERAP1; ERAP2; MHC-I; Pancreatic β-cell; Preproinsulin; Viral infections.

Publication types

  • Review

MeSH terms

  • Aminopeptidases / genetics
  • Aminopeptidases / metabolism
  • Diabetes Mellitus, Type 1* / metabolism
  • Endoplasmic Reticulum / metabolism
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Minor Histocompatibility Antigens / metabolism
  • Peptides / chemistry

Substances

  • Aminopeptidases
  • Histocompatibility Antigens Class I
  • Peptides
  • Minor Histocompatibility Antigens
  • ERAP1 protein, human
  • ERAP2 protein, human