Pericytes take up and degrade α-synuclein but succumb to apoptosis under cellular stress

Sci Rep. 2022 Oct 15;12(1):17314. doi: 10.1038/s41598-022-20261-0.

Abstract

Parkinson's disease (PD) is characterised by the progressive loss of midbrain dopaminergic neurons and the presence of aggregated α-synuclein (α-syn). Pericytes and microglia, two non-neuronal cells contain α-syn in the human brain, however, their role in disease processes is poorly understood. Pericytes, found surrounding the capillaries in the brain are important for maintaining the blood-brain barrier, controlling blood flow and mediating inflammation. In this study, primary human brain pericytes and microglia were exposed to two different α-synuclein aggregates. Inflammatory responses were assessed using immunocytochemistry, cytometric bead arrays and proteome profiler cytokine array kits. Fixed flow cytometry was used to investigate the uptake and subsequent degradation of α-syn in pericytes. We found that the two α-syn aggregates are devoid of inflammatory and cytotoxic actions on human brain derived pericytes and microglia. Although α-syn did not induce an inflammatory response, pericytes efficiently take up and degrade α-syn through the lysosomal pathway but not the ubiquitin-proteasome system. Furthermore, when pericytes were exposed the ubiquitin proteasome inhibitor-MG132 and α-syn aggregates, there was profound cytotoxicity through the production of reactive oxygen species resulting in apoptosis. These results suggest that the observed accumulation of α-syn in pericytes in human PD brains likely plays a role in PD pathogenesis, perhaps by causing cerebrovascular instability, under conditions of cellular stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Cytokines / metabolism
  • Humans
  • Parkinson Disease* / metabolism
  • Pericytes / metabolism
  • Proteasome Endopeptidase Complex / metabolism
  • Proteasome Inhibitors / metabolism
  • Proteome / metabolism
  • Reactive Oxygen Species / metabolism
  • Ubiquitin / metabolism
  • alpha-Synuclein* / metabolism

Substances

  • Cytokines
  • Proteasome Inhibitors
  • Proteome
  • Reactive Oxygen Species
  • Ubiquitin
  • alpha-Synuclein
  • Proteasome Endopeptidase Complex