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α-Synuclein Penetrates Mucin Hydrogels Despite Its Mucoadhesive Properties.

Matthias MarczynskiCarolin A RickertSlav A SemerdzhievWouter R van DijkIne M J Segers-NoltenMireille M A E ClaessensOliver Lieleg
Published in: Biomacromolecules (2019)
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.
Keyphrases
  • drug delivery
  • spinal cord
  • induced apoptosis
  • hyaluronic acid
  • gene expression
  • extracellular matrix
  • wound healing
  • oxidative stress