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LV23007

Dioscuri Centre for Stem Cell Biology and Metabolic Diseases

Public support

  • Provider

    Ministry of Education, Youth and Sports

  • Programme

  • Call for proposals

  • Main participants

    Masarykova univerzita / Přírodovědecká fakulta

  • Contest type

    M2 - International cooperation

  • Contract ID

    MSMT-22090/2023-5

Alternative language

  • Project name in Czech

    Dioscuri Centre for Stem Cell Biology and Metabolic Diseases

  • Annotation in Czech

    The continued health of many of our organs, including the skeleton, relies on the function of specialized stem cells (SCs). These SCs reside in NICHES that support their long-term maintenance. Disruption of the NICHE, due to aging, injury, or genetic mutations, can lead to declines in SCs and a failure to maintain and repair tissues. Compared to our understanding of the SCs that maintain and repair our skeleton, we know much less about the cell types that constitute their NICHE. My prior large-scale genomics studies have uncovered a novel NICHE cell type for the skeleton. Intriguingly, these NICHE cells are defined by a unique metabolic profile, in particular enzymes for Phenylalanine/Tyrosine (Phe/Tyr) metabolism and glycogen synthesis. Mutations in Phe/Tyr metabolism genes lead to skeletal diseases in humans, HGD (Alkaptonuria, aka "black bone disease") and PAH (Phenylketonuria), suggesting a critical role of metabolism in NICHE cells to support the SC that maintain the skeleton. I have generated the first animal model for Alkaptonuria; hgd mutant zebrafish that fully recapitulates the black bone phenotype of human patients. I will establish a research centre that leverages the powerful genomic, genetic, and high-resolution imaging strengths of zebrafish to test the roles of metabolism in SC maintenance. Findings from my proposed studies will inform future therapies aimed at correcting metabolic diseases and restoring SC function and skeletal health by modulating the NICHE.

Scientific branches

  • R&D category

    ZV - Basic research

  • OECD FORD - main branch

    10601 - Cell biology

  • OECD FORD - secondary branch

  • OECD FORD - another secondary branch

  • CEP - equivalent branches <br>(according to the <a href="http://www.vyzkum.cz/storage/att/E6EF7938F0E854BAE520AC119FB22E8D/Prevodnik_oboru_Frascati.pdf">converter</a>)

    EA - Morphology and cytology

Solution timeline

  • Realization period - beginning

    Jul 1, 2024

  • Realization period - end

    Jun 30, 2029

  • Project status

    B - Running multi-year project

  • Latest support payment

    Oct 4, 2024

Data delivery to CEP

  • Confidentiality

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

  • Data delivery code

    CEP25-MSM-LV-R

  • Data delivery date

    Feb 20, 2025

Finance

  • Total approved costs

    35,504 thou. CZK

  • Public financial support

    32,515 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    2,989 thou. CZK