The autoimmune response induced by α-synuclein peptides drives neuronal cell death and glial cell activation

J Autoimmun. 2024 Jul:147:103256. doi: 10.1016/j.jaut.2024.103256. Epub 2024 May 24.

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disorder associated with the loss of dopaminergic neurons and neuroinflammation. Recent studies have identified a role of T cells in the pathogenesis of PD. Additionally, these studies suggested that α-synuclein (α-Syn) is related to abnormal T-cell responses and may act as an epitope and trigger autoimmune T-cell responses. However, it is unclear whether the α-Syn-mediated autoimmune response occurs and whether it is related to neuronal cell death and glial cell activation. In this study, we investigated the autoimmune T-cell response induced by α-Syn peptides and evaluated the neurotoxic effect of the α-Syn peptide-mediated autoimmune response. The immunization of mice with α-Syn peptides resulted in enhanced autoimmune responses, such as the peptide recall response, polarization toward Th1/Th17 cells, and regulatory T cell imbalance. Furthermore, the α-Syn autoimmune response led to the death of primary neurons cocultured with splenocytes. Treatment with conditioned media from α-Syn peptide-immunized splenocytes induced microglia and toxic A1-type astrocyte activation. Taken together, our results provide evidence of the potential role of the α-Syn-initiated autoimmune response and its contribution to neuronal cell death and glial cell activation.

Keywords: Autoimmune response; Glial cell activation; Neuronal cell death; Parkinson's disease; T cell; α-Syn peptide; α-Synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmunity*
  • Cell Death* / drug effects
  • Cells, Cultured
  • Female
  • Humans
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology
  • Mice
  • Mice, Inbred C57BL
  • Neuroglia / drug effects
  • Neuroglia / immunology
  • Neuroglia / metabolism
  • Neurons* / immunology
  • Neurons* / metabolism
  • Neurons* / pathology
  • Parkinson Disease / immunology
  • Parkinson Disease / metabolism
  • Parkinson Disease / pathology
  • Peptides / immunology
  • T-Lymphocytes, Regulatory / immunology
  • alpha-Synuclein* / immunology
  • alpha-Synuclein* / metabolism

Substances

  • alpha-Synuclein
  • Peptides