Download
s00401-020-02178-y.pdf 3,16MB
WeightNameValue
1000 Titel
  • SFPQ and Tau: critical factors contributing to rapid progression of Alzheimer’s disease
1000 Autor/in
  1. Younas, Neelam |
  2. Zafar, Saima |
  3. Shafiq, Mohsin |
  4. Noor, Aneeqa |
  5. Siegert, Anna |
  6. Arora, Amandeep Singh |
  7. Galkin, Alexey |
  8. Zafar, Ayesha |
  9. Schmitz, Mathias |
  10. Stadelmann, Christine |
  11. Andreoletti, Olivier |
  12. Ferrer, Isidre |
  13. Zerr, Inga |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-06-23
1000 Erschienen in
1000 Quellenangabe
  • 140(3):317-339
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-020-02178-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423812/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Dysfunctional RNA-binding proteins (RBPs) have been implicated in several neurodegenerative disorders. Recently, this paradigm of RBPs has been extended to pathophysiology of Alzheimer's disease (AD). Here, we identified disease subtype specific variations in the RNA-binding proteome (RBPome) of sporadic AD (spAD), rapidly progressive AD (rpAD), and sporadic Creutzfeldt Jakob disease (sCJD), as well as control cases using RNA pull-down assay in combination with proteomics. We show that one of these identified proteins, splicing factor proline and glutamine rich (SFPQ), is downregulated in the post-mortem brains of rapidly progressive AD patients, sCJD patients and 3xTg mice brain at terminal stage of the disease. In contrast, the expression of SFPQ was elevated at early stage of the disease in the 3xTg mice, and in vitro after oxidative stress stimuli. Strikingly, in rpAD patients' brains SFPQ showed a significant dislocation from the nucleus and cytoplasmic colocalization with TIA-1. Furthermore, in rpAD brain lesions, SFPQ and p-tau showed extranuclear colocalization. Of note, association between SFPQ and tau-oligomers in rpAD brains suggests a possible role of SFPQ in oligomerization and subsequent misfolding of tau protein. In line with the findings from the human brain, our in vitro study showed that SFPQ is recruited into TIA-1-positive stress granules (SGs) after oxidative stress induction, and colocalizes with tau/p-tau in these granules, providing a possible mechanism of SFPQ dislocation through pathological SGs. Furthermore, the expression of human tau in vitro induced significant downregulation of SFPQ, suggesting a causal role of tau in the downregulation of SFPQ. The findings from the current study indicate that the dysregulation and dislocation of SFPQ, the subsequent DNA-related anomalies and aberrant dynamics of SGs in association with pathological tau represents a critical pathway which contributes to rapid progression of AD.
1000 Sacherschließung
lokal Creutzfeldt-Jakob Syndrome/metabolism [MeSH]
lokal Brain/pathology [MeSH]
lokal RNA-Binding Proteins/metabolism [MeSH]
lokal Humans [MeSH]
lokal RNA-binding proteins
lokal Cytoplasm/metabolism [MeSH]
lokal Animals [MeSH]
lokal Stress granules
lokal PTB-Associated Splicing Factor/metabolism [MeSH]
lokal Rapidly progressive Alzheimer’s disease
lokal Mice, Transgenic [MeSH]
lokal Down-Regulation/physiology [MeSH]
lokal RNA-Binding Proteins/genetics [MeSH]
lokal Brain/metabolism [MeSH]
lokal Original Paper
lokal 3xTg mice
lokal Alzheimer Disease/metabolism [MeSH]
lokal Dislocation
lokal SFPQ
lokal tau Proteins/metabolism [MeSH]
lokal Alzheimer Disease/pathology [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/WW91bmFzLCBOZWVsYW0=|https://frl.publisso.de/adhoc/uri/WmFmYXIsIFNhaW1h|https://frl.publisso.de/adhoc/uri/U2hhZmlxLCBNb2hzaW4=|https://frl.publisso.de/adhoc/uri/Tm9vciwgQW5lZXFh|https://frl.publisso.de/adhoc/uri/U2llZ2VydCwgQW5uYQ==|https://frl.publisso.de/adhoc/uri/QXJvcmEsIEFtYW5kZWVwIFNpbmdo|https://frl.publisso.de/adhoc/uri/R2Fsa2luLCBBbGV4ZXk=|https://frl.publisso.de/adhoc/uri/WmFmYXIsIEF5ZXNoYQ==|https://frl.publisso.de/adhoc/uri/U2NobWl0eiwgTWF0aGlhcw==|https://frl.publisso.de/adhoc/uri/U3RhZGVsbWFubiwgQ2hyaXN0aW5l|https://frl.publisso.de/adhoc/uri/QW5kcmVvbGV0dGksIE9saXZpZXI=|https://frl.publisso.de/adhoc/uri/RmVycmVyLCBJc2lkcmU=|https://frl.publisso.de/adhoc/uri/WmVyciwgSW5nYQ==
1000 Hinweis
  • DeepGreen-ID: 129b25d1be3d453e80a1e327490defdd ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Dateien
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6466738.rdf
1000 Erstellt am 2023-11-17T02:35:52.672+0100
1000 Erstellt von 322
1000 beschreibt frl:6466738
1000 Zuletzt bearbeitet Fri Dec 01 04:46:39 CET 2023
1000 Objekt bearb. Fri Dec 01 04:46:39 CET 2023
1000 Vgl. frl:6466738
1000 Oai Id
  1. oai:frl.publisso.de:frl:6466738 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

View source