Dataset DZNE-2023-00186

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Dataset: Cerebrospinal Fluid (CSF) Proteomics of A30P-αS mice

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2022
PRoteomics IDEntifications Database

PRoteomics IDEntifications Database ()

Abstract: Here, we took advantage of well-defined mouse models for α-synucleinopathy (A30P-αS ) to explore proteome changes in the cerebrospinal fluid which are related to these distinct proteopathic lesions. Non-targeted liquid chromatography-mass spectrometry revealed that the majority of proteins that undergo age- and disease-related changes in either mouse model was linked to microglia, and more specifically to previously described disease state-specific microglia transcriptomic signatures. The finding that such transcriptomic changes translate into corresponding protein changes in cerebrospinal fluid is of high clinical relevance, supporting efforts to identify bodily fluid biomarkers that reflect the various functional states of microglial activation in Parkinson’s disease.


Contributing Institute(s):
  1. Neuroproteomics (AG Lichtenthaler)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Appears in the scientific report 2022
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The record appears in these collections:
Document types > Other Resources > Datasets
Institute Collections > M DZNE > M DZNE-AG Lichtenthaler
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Publications Database


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Signatures of glial activity can be detected in the CSF proteome
Proceedings of the National Academy of Sciences of the United States of America 119(24), e2119804119 () [10.1073/pnas.2119804119] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS


 Record created 2023-01-27, last modified 2025-01-27


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