Novel strategies for targeting cellular senescence
Novel strategies for targeting cellular senescence
Disciplines
Biology (50%); Clinical Medicine (30%); Medical-Theoretical Sciences, Pharmacy (20%)
Keywords
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Senescence,
Mitochondria,
Inter-Organelle Communication,
Proteostasis,
Nutrient Signaling,
Biological Aging
Aging is a complex process driving the progressive functional decline of various tissues. The FWF research group "SENIOPROM" aims to better understand the molecular mechanisms that contribute to cell aging, also known as cellular senescence. In mammals, including humans, senescent cells accumulate during aging, compromise organs` function, and contribute to various age-related diseases. In the SENIOPROM project, we aim to elucidate how the interplay of mitochondria with other organelles, new mechanisms of metabolic regulation, and the maintenance of functional proteins contribute to cell senescence. Based on these subcellular processes, we aim to develop and characterize new small molecules that selectively remove senescent cells or render them harmless. We utilize cell cultures, different model organisms, and simplified artificial human organs to investigate mechanisms and test potential new treatment strategies. SENIOPROM generates added value through the interdisciplinary collaboration between molecular and cell biology, biotechnology, pharmacology, and computational and medicinal chemistry. The consortium involves three recently established PIs working at the University of Innsbruck (Teresa Kaserer), the Medical University of Graz (Corina Madreiter-Sokolowski), and the Medical University of Vienna (Markus Schosserer) with one well-established expert in senescence research from the Institute for Biomedical Aging Research at Innsbruck University, Pidder Jansen-Dürr, who will also serve as coordinator of the SENIOPROM project. Further information can be found at www.senioprom.com.
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consortium member (01.03.2023 -)
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consortium member (01.03.2023 -)
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consortium member (01.03.2023 -)
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consortium member (01.03.2023 -)
- Universität Innsbruck
- Johannes Grillari, Ludwig Boltzmann Gesellschaft , national collaboration partner
- Gerd Leitinger, Medizinische Universität Graz , national collaboration partner
- Hubert Gstach, Universität Wien , national collaboration partner
Research Output
- 24 Citations
- 5 Publications
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2025
Title A novel super-resolution STED microscopy analysis approach to observe spatial MCU and MICU1 distribution dynamics in cells DOI 10.1016/j.bbamcr.2025.119900 Type Journal Article Author Hirtl M Journal Biochimica et Biophysica Acta (BBA) - Molecular Cell Research Pages 119900 Link Publication -
2024
Title Targeting organ-specific mitochondrial dysfunction to improve biological aging DOI 10.1016/j.pharmthera.2024.108710 Type Journal Article Author Madreiter-Sokolowski C Journal Pharmacology & Therapeutics Pages 108710 Link Publication -
2024
Title In vitro examination of Piezo1-TRPV4 dynamics: implications for placental endothelial function in normal and preeclamptic pregnancies DOI 10.1152/ajpcell.00794.2024 Type Journal Article Author Allerkamp H Journal American Journal of Physiology-Cell Physiology -
2024
Title 2'-O-ribose methylation levels of ribosomal RNA distinguish different types of growth arrest in human dermal fibroblasts DOI 10.1242/jcs.261930 Type Journal Article Author Yang G Journal Journal of Cell Science Link Publication -
2024
Title Mitochondrial Dysfunction in Endothelial Progenitor Cells: Unraveling Insights from Vascular Endothelial Cells DOI 10.3390/biology13020070 Type Journal Article Author Kulovic-Sissawo A Journal Biology Pages 70 Link Publication