Unraveling α-synuclein and amylin co-aggregation: pathological insights and biomarker development for Parkinson's disease

Theranostics. 2025 Jun 20;15(15):7409-7424. doi: 10.7150/thno.112396. eCollection 2025.

Abstract

Background: Patients with diabetes have a higher morbidity in Parkinson's disease (PD) than others, but the mechanism underlying this link remains controversial. The co-aggregation of α-synuclein (α-syn) and amylin has been hypothesized as a key contributor. Methods: Molecular interaction analysis and co-immunoprecipitation were conducted to assess the feasibility of co-aggregation. We developed a tailored surface-based fluorescence distribution method to detect the co-aggregate in the subject's serum sample and brain-derived L1CAM-positive Extracellular Vesicles. Subjects include Health Controls (HC), PD patients and multiple system atrophy (MSA) patients. Results: The co-aggregates were detected in PD patient samples, in both serum and brain-derived extracellular vesicles (EVs). We demonstrated that the co-aggregate count could distinguish PD patients from healthy individuals. Our results revealed a positive correlation between co-aggregate count and Parkinson's disease scales or diabetes markers, highlighting the role of co-aggregation in promoting PD progression. The distribution of co-aggregates demonstrated diversity among different α-synucleinopathies; a high co-aggregates count was found in EVs and serum of PD patients, but not in the serum of MSA patients. Conclusion: The existence of α-syn-amylin co-aggregates was confirmed. Our findings suggest that α-syn-amylin co-aggregation may play a pivotal role in PD pathology, and have the potential as a biomarker. These results point to a potential path for early-diagnosis and therapeutic intervention.

MeSH terms

  • Aged
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Brain / metabolism
  • Brain / pathology
  • Extracellular Vesicles / metabolism
  • Female
  • Humans
  • Islet Amyloid Polypeptide* / blood
  • Islet Amyloid Polypeptide* / metabolism
  • Male
  • Middle Aged
  • Multiple System Atrophy / blood
  • Multiple System Atrophy / metabolism
  • Multiple System Atrophy / pathology
  • Parkinson Disease* / blood
  • Parkinson Disease* / diagnosis
  • Parkinson Disease* / metabolism
  • Parkinson Disease* / pathology
  • Protein Aggregates
  • alpha-Synuclein* / blood
  • alpha-Synuclein* / metabolism

Substances

  • alpha-Synuclein
  • Islet Amyloid Polypeptide
  • Biomarkers
  • SNCA protein, human
  • Protein Aggregates