| Literature DB >> 36229715 |
Rui Wang1,2, Haigang Ren2, Elena Kaznacheyeva3, Xiaojun Lu4, Guanghui Wang5,6.
Abstract
The accumulation of pathological α-synuclein (α-syn) in the central nervous system and the progressive loss of dopaminergic neurons in the substantia nigra pars compacta are the neuropathological features of Parkinson's disease (PD). Recently, the findings of prion-like transmission of α-syn pathology have expanded our understanding of the region-specific distribution of α-syn in PD patients. Accumulating evidence suggests that α-syn aggregates are released from neurons and endocytosed by glial cells, which contributes to the clearance of α-syn. However, the activation of glial cells by α-syn species produces pro-inflammatory factors that decrease the uptake of α-syn aggregates by glial cells and promote the transmission of α-syn between neurons, which promotes the spread of α-syn pathology. In this article, we provide an overview of current knowledge on the role of glia and α-syn pathology in PD pathogenesis, highlighting the relationships between glial responses and the spread of α-syn pathology.Entities:
Keywords: Astrocyte activation; Microglial activation; Neuroinflammation; Parkinson's disease; α-synuclein pathology
Year: 2022 PMID: 36229715 DOI: 10.1007/s12264-022-00957-z
Source DB: PubMed Journal: Neurosci Bull ISSN: 1995-8218 Impact factor: 5.271