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Restoring LSECtin expression in cirrhosis

Restoring LSECtin expression in cirrhosis

Benedikt Michael Simbrunner (ORCID: 0000-0001-8181-9146)
  • Grant DOI 10.55776/J4934
  • Funding program Erwin Schrödinger
  • Status ended
  • Start June 1, 2025
  • End October 31, 2025
  • Funding amount € 49,000

Disciplines

Clinical Medicine (100%)

Keywords

    Cirrhosis, LSEC, Portal Hypertension, Inflammation

Abstract

Liver cirrhosis is a serious chronic disease in which healthy liver tissue is gradually replaced by scar tissue due to long-term damage (e.g., from alcohol). As a result, the liver progressively loses its function including its ability to support the immune system. Specialized cells in the livers blood vessels, known as LSEC cells, play a key role in controlling inflammation, but they lose this function in cirrhosis. A planned research project will investigate the role of a protein called LSECtin in these LSEC cells. This protein, which plays an important role in the livers immune system, is no longer produced in sufficient amounts during cirrhosis. The research will examine whether specific immune signaling molecules (interleukins 10 and 13; IL-10 and IL-13) can help restore the production of LSECtin. In a further step, the project will explore whether the production of LSECtin can be stimulated through targeted changes in the way genetic material is packaged so- called epigenetic mechanisms. A substance that directly influences these mechanisms will be used. It will be delivered to the affected cells using tiny transport particles. The project will also analyze liver tissue samples from patients with cirrhosis to compare the findings from laboratory models with real-life disease conditions. The goal is to find new ways to boost LSECtin production and thereby improve the livers immune system in cirrhosis potentially paving the way for future treatment options.

Research institution(s)
  • Universidad Miguel Hernandez - 100%

Research Output

  • 3 Publications
  • 1 Scientific Awards
Publications
  • 2025
    Title Bile acid signaling in MASLD: From pathogenesis to therapeutic applications.
    DOI 10.1097/hep.0000000000001539
    Type Journal Article
    Author Paternostro R
    Journal Hepatology (Baltimore, Md.)
  • 2026
    Title Biomarkers of Extracellular Matrix Remodelling Are Linked to Severity and Outcome of Advanced Chronic Liver Disease.
    DOI 10.1111/apt.70407
    Type Journal Article
    Author Simbrunner B
    Journal Alimentary pharmacology & therapeutics
    Pages 648-661
  • 2025
    Title Antagonizing epigenetically controlled PAF/PAF-R pathway improves liver function during experimental cirrhosis.
    DOI 10.1016/j.biopha.2025.118804
    Type Journal Article
    Author Caparrós E
    Journal Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
    Pages 118804
Scientific Awards
  • 2025
    Title 3nd INTERNATIONAL WORKSHOP ON LIVER AND GUT FIBROSIS
    Type Personally asked as a key note speaker to a conference
    Level of Recognition Continental/International

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