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Time- and dose-dependent seeding tendency of exogenous tau R2 and R3 aggregates in cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15640%2F23%3A73618356" target="_blank" >RIV/61989592:15640/23:73618356 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15110/23:73618356

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0006291X23002425?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0006291X23002425?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.bbrc.2023.02.057" target="_blank" >10.1016/j.bbrc.2023.02.057</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Time- and dose-dependent seeding tendency of exogenous tau R2 and R3 aggregates in cells

  • Original language description

    Tauopathies are a group of neurodegenerative diseases categorised into three types, 3R, 4R, or 3Rþ4R (mixed) tauopathies, based on the tau isoforms that make up the aberrant filaments. It is supposed that all six tau isoforms share functional characteristics. However, differences in the neuropathological features associated with different tauopathies offer the possibility that disease progression and tau accumulation may vary depending on the isoform composition. The presence or absence of repeat 2 (R2) in the microtubule-binding domain defines the type of isoform, which might influence tau pathology associated with a particular tau isoform. Therefore, our study aimed to identify the differences in the seeding propensities of R2 and repeat 3 (R3) aggregates using HEK293T biosensor cells. We show that the seeding induced by R2 was generally higher than by R3 aggregates, and lower concentrations of R2 aggregates are sufficient to induce seeding. Next, we found that both R2 and R3 aggregates dosedependently increased triton-insoluble Ser262 phosphorylation of native tau, which is only visible in cells seeded with higher concentrations (12.5 nM or 100 nM) of R2 and R3 aggregates, despite the seeding by the lower concentrations of R2 aggregates after 72 h. However, the accumulation of tritoninsoluble pSer262 tau was visible earlier in cells induced with R2 than in R3 aggregates. Our findings suggest that the R2 region may contribute to the early and enhanced induction of tau aggregation and define the difference in disease progression and neuropathology of 4R tauopathies.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

  • ISSN

    0006-291X

  • e-ISSN

    1090-2104

  • Volume of the periodical

    653

  • Issue of the periodical within the volume

    31.03.2023

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    4

  • Pages from-to

    102-105

  • UT code for WoS article

    000949585300001

  • EID of the result in the Scopus database

    2-s2.0-85150430796