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Pathogenic Potential of Hic1-Expressing Cardiac Stromal Progenitors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F20%3A00531041" target="_blank" >RIV/68378050:_____/20:00531041 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/journal/cell-stem-cell/vol/26/issue/2" target="_blank" >https://www.sciencedirect.com/journal/cell-stem-cell/vol/26/issue/2</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.stem.2019.12.008" target="_blank" >10.1016/j.stem.2019.12.008</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Pathogenic Potential of Hic1-Expressing Cardiac Stromal Progenitors

  • Original language description

    The cardiac stroma contains multipotent mesenchymal progenitors. However, lineage relationships within cardiac stromal cells are poorly defined. Here, we identified heart-resident PDGFRa(+) SCA-1(+) cells as cardiac fibro/adipogenic progenitors (cFAPs) and show that they respond to ischemic damage by generating fibrogenic cells. Pharmacological blockade of this differentiation step with an anti-fibrotic tyrosine kinase inhibitor decreases post-myocardial infarction (post-MI) remodeling and leads to improvement in cardiac function. In the undamaged heart, activation of cFAPs through lineage-specific deletion of the gene encoding the quiescence-associated factor HIC1 reveals additional pathogenic potential, causing fibrofatty infiltration within the myocardium and driving major pathological features pathognomonic in arrhythmogenic cardiomyopathy (AC). In this regard, cFAPs contribute to multiple pathogenic cell types within cardiac tissue and therapeutic strategies aimed at modifying their activity are expected to have tremendous benefit for the treatment of diverse cardiac diseases.

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cell Stem Cell

  • ISSN

    1934-5909

  • e-ISSN

  • Volume of the periodical

    26

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    16

  • Pages from-to

    205-220

  • UT code for WoS article

    000512951100011

  • EID of the result in the Scopus database