دورية أكاديمية

The major histocompatibility complex participates in Parkinson’s disease

التفاصيل البيبلوغرافية
العنوان: The major histocompatibility complex participates in Parkinson’s disease
المؤلفون: Rou Gu, Jianyu Pan, Maher Un Nisa Awan, Xiaowei Sun, Fang Yan, Liping Bai, Jie Bai
المصدر: Pharmacological Research, Vol 203, Iss , Pp 107168- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: Parkinson’s disease, major histocompatibility complex, immune response, inflammation reaction, Therapeutics. Pharmacology, RM1-950
الوصف: Parkinson’s disease (PD) is a common neurodegenerative disease characterized by progressive loss of dopaminergic neurons in the substantia nigra and the aggregation of alpha-synuclein (α-syn). The central nervous system (CNS) has previously been considered as an immune-privileged area. However, studies have shown that the immune responses are involved in PD. The major histocompatibility complex (MHC) presents antigens from antigen-presenting cells (APCs) to T lymphocytes, immune responses will be induced. MHCs are expressed in microglia, astrocytes, and dopaminergic neurons. Single nucleotide polymorphisms in MHC are related to the risk of PD. The aggregated α-syn triggers the expression of MHCs by activating glia cells. CD4+ and CD8+ T lymphocytes responses and microglia activation are detected in brains of PD patients. In addiction immune responses further increase blood-brain barrier (BBB) permeability and T cell infiltration in PD. Thus, MHCs are involved in PD through participating in immune and inflammatory responses.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1096-1186
Relation: http://www.sciencedirect.com/science/article/pii/S1043661824001129; https://doaj.org/toc/1096-1186
DOI: 10.1016/j.phrs.2024.107168
URL الوصول: https://doaj.org/article/027dad0149d6499ba44b382a3dcaf2dd
رقم الأكسشن: edsdoj.027dad0149d6499ba44b382a3dcaf2dd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10961186
DOI:10.1016/j.phrs.2024.107168