Tau-FG-nucleoporin98 interaction and impaired nucleocytoplasmic transport in Alzheimer's disease
© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissionsoup.com..
An emerging pathophysiology associated with the neurodegenerative Alzheimer's disease (AD) is the impairment of nucleocytoplasmic transport (NCT). The impairment can originate from damage to the nuclear pore complex (NPC) or other factors involved in NCT. The phenylalanine-glycine nucleoporins (FG-Nups) form a crucial component of the NPC, which is central to NCT. Recent discoveries have highlighted that the neuropathological protein tau is involved in direct interactions with the FG-Nups and impairment of the NCT process. Targeting such interactions may lead to the identification of novel interaction inhibitors and offer new therapeutic alternatives for the treatment of AD. This review highlights recent findings associated with impaired NCT in AD and the interaction between tau and the FG-Nups.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:22 |
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Enthalten in: |
Briefings in functional genomics - 22(2023), 2 vom: 13. Apr., Seite 161-167 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Nag, Niharika [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 17.04.2023 Date Revised 12.05.2023 published: Print Citation Status MEDLINE |
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doi: |
10.1093/bfgp/elac022 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM344426610 |
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520 | |a An emerging pathophysiology associated with the neurodegenerative Alzheimer's disease (AD) is the impairment of nucleocytoplasmic transport (NCT). The impairment can originate from damage to the nuclear pore complex (NPC) or other factors involved in NCT. The phenylalanine-glycine nucleoporins (FG-Nups) form a crucial component of the NPC, which is central to NCT. Recent discoveries have highlighted that the neuropathological protein tau is involved in direct interactions with the FG-Nups and impairment of the NCT process. Targeting such interactions may lead to the identification of novel interaction inhibitors and offer new therapeutic alternatives for the treatment of AD. This review highlights recent findings associated with impaired NCT in AD and the interaction between tau and the FG-Nups | ||
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