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1000 Titel
  • Congenic expression of poly-GA but not poly-PR in mice triggers selective neuron loss and interferon responses found in C9orf72 ALS
1000 Autor/in
  1. LaClair, Katherine D. |
  2. Zhou, Qihui |
  3. Michaelsen, Meike |
  4. Wefers, Benedikt |
  5. Brill, Monika S. |
  6. Janjic, Aleksandar |
  7. Rathkolb, Birgit |
  8. Farny, Daniel |
  9. Cygan, Mikolaj |
  10. de Angelis, Martin Hrabe |
  11. Wurst, Wolfgang |
  12. Neumann, Manuela |
  13. Enard, Wolfgang |
  14. Misgeld, Thomas |
  15. Arzberger, Thomas |
  16. Edbauer, Dieter |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-06-19
1000 Erschienen in
1000 Quellenangabe
  • 140(2):121-142
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-020-02176-0 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7360660/ |
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
lokal Interferon
lokal Amyotrophic Lateral Sclerosis/pathology [MeSH]
lokal C9orf72 Protein/genetics [MeSH]
lokal Microglia
lokal Nerve Degeneration/immunology [MeSH]
lokal Animals [MeSH]
lokal DNA Repeat Expansion/genetics [MeSH]
lokal Mice, Transgenic [MeSH]
lokal Neurodegeneration
lokal Mice [MeSH]
lokal FTD
lokal Mouse model
lokal Original Paper
lokal ALS
lokal Interferons/biosynthesis [MeSH]
lokal Neurons/pathology [MeSH]
lokal Amyotrophic Lateral Sclerosis/genetics [MeSH]
lokal Amyotrophic Lateral Sclerosis/immunology [MeSH]
lokal Nerve Degeneration/pathology [MeSH]
lokal Disease Models, Animal [MeSH]
lokal Nerve Degeneration/genetics [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TGFDbGFpciwgS2F0aGVyaW5lIEQu|https://frl.publisso.de/adhoc/uri/WmhvdSwgUWlodWk=|https://frl.publisso.de/adhoc/uri/TWljaGFlbHNlbiwgTWVpa2U=|https://frl.publisso.de/adhoc/uri/V2VmZXJzLCBCZW5lZGlrdA==|https://frl.publisso.de/adhoc/uri/QnJpbGwsIE1vbmlrYSBTLg==|https://frl.publisso.de/adhoc/uri/SmFuamljLCBBbGVrc2FuZGFy|https://frl.publisso.de/adhoc/uri/UmF0aGtvbGIsIEJpcmdpdA==|https://frl.publisso.de/adhoc/uri/RmFybnksIERhbmllbA==|https://frl.publisso.de/adhoc/uri/Q3lnYW4sIE1pa29sYWo=|https://frl.publisso.de/adhoc/uri/ZGUgQW5nZWxpcywgTWFydGluIEhyYWJl|https://frl.publisso.de/adhoc/uri/V3Vyc3QsIFdvbGZnYW5n|https://frl.publisso.de/adhoc/uri/TmV1bWFubiwgTWFudWVsYQ==|https://frl.publisso.de/adhoc/uri/RW5hcmQsIFdvbGZnYW5n|https://frl.publisso.de/adhoc/uri/TWlzZ2VsZCwgVGhvbWFz|https://frl.publisso.de/adhoc/uri/QXJ6YmVyZ2VyLCBUaG9tYXM=|https://orcid.org/0000-0002-7186-4653
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1000 Erstellt am 2023-11-17T02:36:53.280+0100
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