Počet záznamů: 1  

USP8 inhibition regulates autophagy flux and controls Salmonella infection

  1. 1.
    SYSNO ASEP0571023
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevUSP8 inhibition regulates autophagy flux and controls Salmonella infection
    Tvůrce(i) Santelices, J. (US)
    Ou, M. (US)
    Maegawa, G. H. B. (US)
    Hercík, Kamil (UOCHB-X)
    Edelmann, M. J. (US)
    Číslo článku1070271
    Zdroj.dok.Frontiers in Cellular and Infection Microbiology. - : Frontiers Media - ISSN 2235-2988
    Roč. 13, March (2023)
    Poč.str.12 s.
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovadeubiquitinating enzymes ; deubiquitinases ; Salmonella ; USP8 ; autophagy ; chemical proteomics
    Obor OECDMedicinal chemistry
    Způsob publikováníOpen access
    Institucionální podporaUOCHB-X - RVO:61388963
    UT WOS000962124300001
    EID SCOPUS85151509577
    DOI10.3389/fcimb.2023.1070271
    AnotaceIntroduction: Ubiquitination is an important protein modification that regulates various essential cellular processes, including the functions of innate immune cells. Deubiquitinases are enzymes responsible for removing ubiquitin modification from substrates, and the regulation of deubiquitinases in macrophages during infection with Salmonella Typhimurium and Yersinia enterocolitica remains unknown. Methods: To identify deubiquitinases regulated in human macrophages during bacterial infection, an activity-based proteomics screen was conducted. The effects of pharmacological inhibition of the identified deubiquitinase, USP8, were examined, including its impact on bacterial survival within macrophages and its role in autophagy regulation during Salmonella infection. Results: Several deubiquiitnases were differentially regulated in infected macrophages. One of the deubiquitinases identified was USP8, which was downregulated upon Salmonella infection. Inhibition of USP8 was associated with a decrease in bacterial survival within macrophages, and it was found to play a distinct role in regulating autophagy during Salmonella infection. The inhibition of USP8 led to the downregulation of the p62 autophagy adaptor. Discussion: The findings of this study suggest a novel role of USP8 in regulating autophagy flux, which restricts intracellular bacteria, particularly during Salmonella infection.
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
    Rok sběru2024
    Elektronická adresahttps://doi.org/10.3389/fcimb.2023.1070271
Počet záznamů: 1  

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