TY - JOUR
T1 - α-Synuclein Penetrates Mucin Hydrogels despite Its Mucoadhesive Properties
AU - Marczynski, Matthias
AU - Rickert, Carolin A.
AU - Semerdzhiev, Slav A.
AU - Van Dijk, Wouter R.
AU - Segers-Nolten, Ine M.J.
AU - Claessens, Mireille M.A.E.
AU - Lieleg, Oliver
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/12/9
Y1 - 2019/12/9
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85075696584&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.9b00905
DO - 10.1021/acs.biomac.9b00905
M3 - Article
C2 - 31721560
AN - SCOPUS:85075696584
SN - 1525-7797
VL - 20
SP - 4332
EP - 4344
JO - Biomacromolecules
JF - Biomacromolecules
IS - 12
ER -