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Projekt Druckansicht

Einfluss von Integrin-linked kinase auf Haut Homöostase und Hautkarzinogenese

Fachliche Zuordnung Dermatologie
Förderung Förderung von 2014 bis 2018
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 262258314
 
Erstellungsjahr 2018

Zusammenfassung der Projektergebnisse

The aim of this project was to understand the role of the niche in SC homeostasis and cancer, and in particular the role of the niche extracellular matrix (ECM) and cell-matrix interactions in this process. We particularly focused on cell-ECM interaction-mediated signaling through a central adaptor Integrin-linked kinase (ILK) in SC homeostasis and carcinogenesis of the skin. Using the HF as a paradigm for a SC niche we obseved that ILK is required for maintaining the SC niche. Deletion of ILK led to enhanced activation of HFSCs, ultimately resulting in their exhaustion. This was due to altered remodelling of the BM within the SC niche, promoting sustained activation of Wnt and Tgf-β2 pathways and a failure to reestablish quiescence. The enhanced SC activity led to increased replicative stress and DNA damage, which predisposed the ILK-deficient epidermis to skin carcinogenesis. Taken together this data indicates that ILK-mediated remodelling of the niche plays an essential role in SC fate regulation and skin homeostasis. In the second part of the project, we built on the knowledge on the importance of the ECM and the microenvironment to identify a specific combination of niche factors that for the first time allowed expansion and long-term maintenance of HFSCs. Utilizing this system we uncovered self-organizing phenotypic plasticity and dynamic bidirectional interconversion between HFSCs and their progeny, providing a cellular mechanism for homeostatic regulation of a SC niche. In summary, our study delineates how reciprocal interaction between SCs and their niches regulate SC fate and highlights the role of tissue architecture in coordinating cellular behaviours and protecting it from malignant transformation.

Projektbezogene Publikationen (Auswahl)

 
 

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