Project: Study of the molecular pathways through which linear (de)ubiquitination governs skin inflammation and aberrant epidermal stem cell activation
2020-01-01 – 2023-12-31
- Abstract
Inflammatory signaling pathways need to be tightly regulated in order to avoid chronic inflammation and the development of inflammatory pathology One of the regulatory proteins responsible for such control is OTULIN, a deubiquitinating enzyme which specifically cleaves linear ubiquitin chains generated by the linear ubiquitin chain assembly complex
We have generated keratinocyte-specific OTULIN knockout mice which develop a severe inflammatory skin condition and exhibit markedly enhanced epidermal stem cell activation In this project, we will investigate the molecular pathways that are affected by the lack of OTULIN in the epithelial cells of the skin, in order to understand how OTULIN regulates inflammatory signaling and cell death responses in the skin Skin harbors many well-characterized stem cell populations and therefore represents an ideal model system to study the intercellular crosstalk between immune cells and stem cells The results of this research will identify crucial mediators of stem cell activation and this knowledge may lay the grounds for novel therapeutic approaches in the treatment of inflammatory skin disorders
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- Journal Article
- A1
- open access
ATG9A-mediated autophagy prevents inflammatory skin disease by limiting TNFR1-driven STING activation and ZBP1-dependent cell death
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- Journal Article
- A1
- open access
Colibactin-driven colon cancer requires adhesin-mediated epithelial binding
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- Journal Article
- A1
- open access
NLRP3 inflammasome activation and pyroptosis are dispensable for tau pathology
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OTULIN as a crucial regulator of keratinocyte death, stem cell identity and Wnt signaling
(2024) -
- Journal Article
- A1
- open access
Cell death as an architect of adult skin stem cell niches
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- Journal Article
- A1
- open access
Myeloid A20 is critical for alternative macrophage polarization and type-2 immune-mediated helminth resistance
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- Miscellaneous
- open access
A20 : a jack of all trades
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- Journal Article
- A1
- open access
Inflammasome signaling is dispensable for ß-amyloid-induced neuropathology in preclinical models of Alzheimer's disease
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- Journal Article
- A1
- open access
Myeloid OTULIN deficiency couples RIPK3-dependent cell death to Nlrp3 inflammasome activation and IL-1β secretion
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- Journal Article
- A1
- open access
Protein citrullination and NET formation do not contribute to the pathology of A20/TNFAIP3 mutant mice