Wiederherstellung von LSECtin Expression bei Leberzirrhose
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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.
| Title | Year(s) | DOI / Link |
|---|---|---|
| Antagonizing epigenetically controlled PAF/PAF-R pathway improves liver function during experimental cirrhosisBiomedicine & Pharmacotherapy | 2025 | 10.1016/j.biopha.2025.118804 |
| Bile acid signaling in MASLD: From pathogenesis to therapeutic applications. |
No additional funding sources recorded.
| 2025 |
| 10.1097/hep.0000000000001539 |
| Biomarkers of Extracellular Matrix Remodelling Are Linked to Severity and Outcome of Advanced Chronic Liver DiseaseAlimentary Pharmacology & Therapeutics | 2025 | 10.1111/apt.70407 |