The autoimmune response induced by α-synuclein peptides drives neuronal cell death and glial cell activation.
Yong-Ho ChoeMin Gi JoBo Gyu KimSangwon LeeBina LeeSeon-Hee KimHyemin SeongWoong-Sun YooMinkyeong KimDong-Kun LeeSeong Jae KimSeung Pil YunMingyo KimPublished in: Journal of autoimmunity (2024)
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.
Keyphrases
- cell death
- multiple sclerosis
- drug induced
- single cell
- cell cycle arrest
- spinal cord
- traumatic brain injury
- cell therapy
- bone marrow
- neuropathic pain
- induced apoptosis
- type diabetes
- skeletal muscle
- mass spectrometry
- oxidative stress
- endoplasmic reticulum stress
- mesenchymal stem cells
- climate change
- brain injury
- cell proliferation
- high resolution
- stress induced
- endothelial cells
- atomic force microscopy