The effect of cytosolic adaptive responses associated with long-term mitochondrial stress on the Tau protein aggregation.

2019/33/B/NZ3/00533

Keywords

Descriptors

  • NZ3_001: Biologia komórki
  • NZ1_002: Biochemia
  • NZ3_005: Neurobiologia molekularna

Panel

NZ3 – Cellular and developmental biology: cell biology, developmental biology, ageing biology, neurobiology

Host institution

Uniwersytet Warszawski, Centrum Nowych Technologii Uniwersytetu Warszawskiego

Voivodeship: mazowieckie

Other projects carried out by the institution »

Principal investigator (from the host institution)

dr Łukasz Samluk

Number of co-investigators in the project: 3

Call

OPUS 17 – announced on 2019-03-15

Amount awarded
1 491 100 PLN
Project start date
2020-04-23
Project end date
2023-10-22
Project duration
42 months (the same as in the proposal)
Project status
Project settled

Project description

Download the project description in a pdf file

Note — project descriptions were prepared by the authors of the applications themselves and placed in the system in an unchanged form.

Information in the final report

Publication in academic press/journals (2)

  1. Immunoproteasome-specific subunit PSMB9 induction is required to regulate cellular proteostasis upon mitochondrial dysfunction.

    Authors:
    Minji Kim, Remigiusz A. Serwa, Lukasz Samluk, Ida Suppanz, Agata Kodroń, Tomasz M. Stępkowski, Praveenraj Elancheliyan, Biniyam Tsegaye, SilkeOeljeklaus, Michal Wasilewski, Bettina Warscheid, and Agnieszka Chacinska
    Academic press:
    Nature communications (year: 2023, volume: 14, pages: Article number: 4092), Publisher: Nature Portfolio
    Status:
    Published
    DOI:
    10.1038/s41467-023-39642-8 – link to the publication
  2. Long-term mitochondrial stress induces early steps of Tau aggregation by increasing reactive oxygen species levels and affecting cellular proteostasis.

    Authors:
    Lukasz Samluk*, Piotr Ostapczuk, and Magdalena Dziembowska
    Academic press:
    Molecular Biology of the Cell (MBoC) (year: 2022, volume: 33, pages: ar67), Publisher: American Society of Cell Biology
    Status:
    Published
    DOI:
    10.1091/mbc.E21-11-0553 – link to the publication

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