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1000 Titel
  • Circular RNA profiling distinguishes medulloblastoma groups and shows aberrant RMST overexpression in WNT medulloblastoma
1000 Autor/in
  1. Rickert, Daniel |
  2. Bartl, Jasmin |
  3. Picard, Daniel |
  4. Bernardi, Flavia |
  5. Qin, Nan |
  6. Lovino, Marta |
  7. Puget, Stéphanie |
  8. Meyer, Frauke-Dorothee |
  9. Mahoungou Koumba, Idriss |
  10. Beez, Thomas |
  11. Varlet, Pascale |
  12. Dufour, Christelle |
  13. Fischer, Ute |
  14. Borkhardt, Arndt |
  15. Reifenberger, Guido |
  16. Ayrault, Olivier |
  17. Remke, Marc |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-17
1000 Erschienen in
1000 Quellenangabe
  • 141(6):975-978
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-021-02306-2 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113310/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Parkinson's disease (PD) is a progressive neurodegenerative disorder that is neuropathologically characterized by degeneration of dopaminergic neurons of the substantia nigra (SN) and formation of Lewy bodies and Lewy neurites composed of aggregated α-synuclein. Proteolysis of α-synuclein by matrix metalloproteinases was shown to facilitate its aggregation and to affect cell viability. One of the proteolysed fragments, Gln79-α-synuclein, possesses a glutamine residue at its N-terminus. We argue that glutaminyl cyclase (QC) may catalyze the pyroglutamate (pGlu)79-α-synuclein formation and, thereby, contribute to enhanced aggregation and compromised degradation of α-synuclein in human synucleinopathies. Here, the kinetic characteristics of Gln79-α-synuclein conversion into the pGlu-form by QC are shown using enzymatic assays and mass spectrometry. Thioflavin T assays and electron microscopy demonstrated a decreased potential of pGlu79-α-synuclein to form fibrils. However, size exclusion chromatography and cell viability assays revealed an increased propensity of pGlu79-α-synuclein to form oligomeric aggregates with high neurotoxicity. In brains of wild-type mice, QC and α-synuclein were co-expressed by dopaminergic SN neurons. Using a specific antibody against the pGlu-modified neo-epitope of α-synuclein, pGlu79-α-synuclein aggregates were detected in association with QC in brains of two transgenic mouse lines with human α-synuclein overexpression. In human brain samples of PD and dementia with Lewy body subjects, pGlu79-α-synuclein was shown to be present in SN neurons, in a number of Lewy bodies and in dystrophic neurites. Importantly, there was a spatial co-occurrence of pGlu79-α-synuclein with the enzyme QC in the human SN complex and a defined association of QC with neuropathological structures. We conclude that QC catalyzes the formation of oligomer-prone pGlu79-α-synuclein in human synucleinopathies, which may-in analogy to pGlu-Aβ peptides in Alzheimer's disease-act as a seed for pathogenic protein aggregation.
1000 Sacherschließung
lokal Pathology
lokal Neurosciences
lokal Correspondence
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/Umlja2VydCwgRGFuaWVs|https://frl.publisso.de/adhoc/uri/QmFydGwsIEphc21pbg==|https://frl.publisso.de/adhoc/uri/UGljYXJkLCBEYW5pZWw=|https://frl.publisso.de/adhoc/uri/QmVybmFyZGksIEZsYXZpYQ==|https://frl.publisso.de/adhoc/uri/UWluLCBOYW4=|https://frl.publisso.de/adhoc/uri/TG92aW5vLCBNYXJ0YQ==|https://frl.publisso.de/adhoc/uri/UHVnZXQsIFN0w6lwaGFuaWU=|https://frl.publisso.de/adhoc/uri/TWV5ZXIsIEZyYXVrZS1Eb3JvdGhlZQ==|https://frl.publisso.de/adhoc/uri/TWFob3VuZ291IEtvdW1iYSwgSWRyaXNz|https://frl.publisso.de/adhoc/uri/QmVleiwgVGhvbWFz|https://frl.publisso.de/adhoc/uri/VmFybGV0LCBQYXNjYWxl|https://frl.publisso.de/adhoc/uri/RHVmb3VyLCBDaHJpc3RlbGxl|https://frl.publisso.de/adhoc/uri/RmlzY2hlciwgVXRl|https://frl.publisso.de/adhoc/uri/Qm9ya2hhcmR0LCBBcm5kdA==|https://frl.publisso.de/adhoc/uri/UmVpZmVuYmVyZ2VyLCBHdWlkbw==|https://frl.publisso.de/adhoc/uri/QXlyYXVsdCwgT2xpdmllcg==|https://orcid.org/0000-0002-9404-9993
1000 Hinweis
  • DeepGreen-ID: 047f0eeb57f04a09b1947734a4cca70f ; 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)
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1000 Erstellt am 2023-05-11T10:41:25.438+0200
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1000 Zuletzt bearbeitet 2023-10-14T01:02:10.996+0200
1000 Objekt bearb. Sat Oct 14 01:02:10 CEST 2023
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