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LH15071

The role of mitochondrial energy metabolism and redox regulations in pulmonary hypertension

Public support

  • Provider

    Ministry of Education, Youth and Sports

  • Programme

    KONTAKT II

  • Call for proposals

    KONTAKT II 5 (SMSM2015LH5)

  • Main participants

    Fyziologický ústav AV ČR, v. v. i.

  • Contest type

    VS - Public tender

  • Contract ID

    MSMT-32267/2015-1

Alternative language

  • Project name in Czech

    Role mitochondriálního energetického a redoxního metabolismu v rozvoji plicní hypertenze

  • Annotation in Czech

    The proposed project will study the detailed role of mitochondrial bioenergetics and redox regulations in initiation and development of pulmonary hypertension induced by chronic hypoxia. We will use the unique biological model, i.e. calf and human fibroblasts derived from pulmonary arteries. The study deals with nowadays widely respected metabolic theory of pulmonary hypertension. We will focus on mitochondria as the principal powerhouse and redox regulator of cellular metabolism. We will uncover changes in substrate distribution for mitochondrial bioenergetics; the role and regulation of suppressed respiratory Complex I activity; the role of reactive oxygen species originated in mitochondria vs. cytosolic compartment and the role of mitochondrial morphology changes in calf and human fibroblasts derived from animals/humans with developed pulmonary hypertension. The uncovered knowledge will be valuable in future for designing of proper therapy for people with pulmonary hypertension.

Scientific branches

  • R&D category

    ZV - Basic research

  • CEP classification - main branch

    ED - Physiology

  • CEP - secondary branch

    FC - Pneumology

  • CEP - another secondary branch

    EA - Morphology and cytology

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

    10601 - Cell biology<br>10602 - Biology (theoretical, mathematical, thermal, cryobiology, biological rhythm), Evolutionary biology<br>30105 - Physiology (including cytology)<br>30203 - Respiratory systems

Completed project evaluation

  • Provider evaluation

    V - Vynikající výsledky projektu (s mezinárodním významem atd.)

  • Project results evaluation

    We uncovered regulatory pathways of energy metabolism and redox state ofpulmonary arterial fibroblasts. Their changes lead to development of pulmonary hypertension. Affected fibroblasts increase their glycolysis vs. mitochondrial oxidation , show prooxidative metabolism, all causing high proliferation and proinflammatory status leading to remodelation of cell wall.

Solution timeline

  • Realization period - beginning

    Jan 1, 2016

  • Realization period - end

    Dec 31, 2017

  • Project status

    U - Finished project

  • Latest support payment

    Mar 2, 2017

Data delivery to CEP

  • Confidentiality

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

  • Data delivery code

    CEP18-MSM-LH-U/01:1

  • Data delivery date

    Jun 7, 2018

Finance

  • Total approved costs

    1,726 thou. CZK

  • Public financial support

    1,726 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    0 thou. CZK