α-突触核蛋白肽诱导的自身免疫反应会导致神经细胞死亡和神经胶质细胞活化。

IF 7.9 1区 医学 Q1 IMMUNOLOGY
Yong-ho Choe , Min Gi Jo , Bo Gyu Kim , Sangwon Lee , Bina Lee , Seon-Hee Kim , Hyemin Seong , Woong-Sun Yoo , Minkyeong Kim , Dong-Kun Lee , Seong Jae Kim , Seung Pil Yun , Mingyo Kim
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引用次数: 0

摘要

帕金森病(PD)是一种进行性神经退行性疾病,与多巴胺能神经元的丧失和神经炎症有关。最近的研究发现了 T 细胞在帕金森病发病机制中的作用。此外,这些研究还表明,α-突触核蛋白(α-Syn)与异常的T细胞反应有关,可能作为表位并引发自身免疫性T细胞反应。然而,α-Syn 介导的自身免疫反应是否发生,是否与神经元细胞死亡和神经胶质细胞活化有关,目前尚不清楚。在这项研究中,我们研究了α-Syn肽诱导的自身免疫T细胞反应,并评估了α-Syn肽介导的自身免疫反应的神经毒性效应。用α-Syn肽免疫小鼠会增强自身免疫反应,如肽召回反应、向Th1/Th17细胞极化和调节性T细胞失衡。此外,α-Syn 自身免疫反应导致与脾脏细胞共培养的初级神经元死亡。用α-Syn肽免疫脾细胞的条件培养基处理可诱导小胶质细胞和毒性A1型星形胶质细胞活化。综上所述,我们的研究结果证明了α-Syn引发的自身免疫反应的潜在作用及其对神经细胞死亡和神经胶质细胞活化的贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The autoimmune response induced by α-synuclein peptides drives neuronal cell death and glial cell activation

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.

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来源期刊
Journal of autoimmunity
Journal of autoimmunity 医学-免疫学
CiteScore
27.90
自引率
1.60%
发文量
117
审稿时长
17 days
期刊介绍: The Journal of Autoimmunity serves as the primary publication for research on various facets of autoimmunity. These include topics such as the mechanism of self-recognition, regulation of autoimmune responses, experimental autoimmune diseases, diagnostic tests for autoantibodies, as well as the epidemiology, pathophysiology, and treatment of autoimmune diseases. While the journal covers a wide range of subjects, it emphasizes papers exploring the genetic, molecular biology, and cellular aspects of the field. The Journal of Translational Autoimmunity, on the other hand, is a subsidiary journal of the Journal of Autoimmunity. It focuses specifically on translating scientific discoveries in autoimmunity into clinical applications and practical solutions. By highlighting research that bridges the gap between basic science and clinical practice, the Journal of Translational Autoimmunity aims to advance the understanding and treatment of autoimmune diseases.
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