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α-Synuclein Penetrates Mucin Hydrogels Despite Its Mucoadhesive Properties.

Authors :
Marczynski M
Rickert CA
Semerdzhiev SA
van Dijk WR
Segers-Nolten IMJ
Claessens MMAE
Lieleg O
Source :
Biomacromolecules [Biomacromolecules] 2019 Dec 09; Vol. 20 (12), pp. 4332-4344. Date of Electronic Publication: 2019 Nov 25.
Publication Year :
2019

Abstract

Recent research indicates that the progression of Parkinson's disease can start from neurons of the enteric nervous system, which are in close contact with the gastrointestinal epithelium: α-synuclein molecules can be transferred from these epithelial cells in a prion-like fashion to enteric neurons. Thin mucus layers constitute a defense line against the exposure of noninfected cells to potentially harmful α-synuclein species. We show that-despite its mucoadhesive properties-α-synuclein can translocate across mucin hydrogels, and this process is accompanied by structural rearrangements of the mucin molecules within the gel. Penetration experiments with different α-synuclein variants and synthetic peptides suggest that two binding sites on α-synuclein are required to accomplish this rearrangement of the mucin matrix. Our results support the notion that the translocation of α-synuclein across mucus barriers observed here might be a critical step in the infection of the gastrointestinal epithelium and the development of Parkinson's disease.

Details

Language :
English
ISSN :
1526-4602
Volume :
20
Issue :
12
Database :
MEDLINE
Journal :
Biomacromolecules
Publication Type :
Academic Journal
Accession number :
31721560
Full Text :
https://doi.org/10.1021/acs.biomac.9b00905