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GDF11 inhibits adipogenesis and improves mature adipocytes metabolic function via WNT/beta-catenin and ALK5/SMAD2/3 pathways

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F22%3A00077732" target="_blank" >RIV/00159816:_____/22:00077732 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/22:00127398

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1111/cpr.13310" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1111/cpr.13310</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/cpr.13310" target="_blank" >10.1111/cpr.13310</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    GDF11 inhibits adipogenesis and improves mature adipocytes metabolic function via WNT/beta-catenin and ALK5/SMAD2/3 pathways

  • Original language description

    Objective: GDF11 is a member of the TGF-beta superfamily that was recently implicated as potential &quot;rejuvenating&quot; factor, which can ameliorate metabolic disorders. The main objective of the presented study was to closely characterize the role of GDF11 signaling in the glucose homeostasis and in the differentiation of white adipose tissue. Methods: We performed microscopy imaging, biochemical and transcriptomic analyses of adipose tissues of 9 weeks old ob/ob mice and murine and human preadipocyte cell lines. Results: Our in vivo experiments employing GDF11 treatment in ob/ob mice showed improved glucose/insulin homeostasis, decreased weight gain and white adipocyte size. Furthermore, GDF11 treatment inhibited adipogenesis in pre-adipocytes by ALK5-SMAD2/3 activation in cooperation with the WNT/beta-catenin pathway, whose inhibition resulted in adipogenic differentiation. Lastly, we observed significantly elevated levels of the adipokine hormone adiponectin and increased glucose uptake by mature adipocytes upon GDF11 exposure. Conclusion: We show evidence that link GDF11 to adipogenic differentiation, glucose, and insulin homeostasis, which are pointing towards potential beneficial effects of GDF11-based &quot;anti-obesity&quot; therapy.

  • 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

    10601 - Cell biology

Result continuities

  • Project

    <a href="/en/project/EF15_003%2F0000492" target="_blank" >EF15_003/0000492: Unveiling the molecular determinants of agingto design new therapeutics</a><br>

  • Continuities

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

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    CELL PROLIFERATION

  • ISSN

    0960-7722

  • e-ISSN

    1365-2184

  • Volume of the periodical

    55

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    15

  • Pages from-to

    nestrankovano

  • UT code for WoS article

    000835228000001

  • EID of the result in the Scopus database