Regulation of Interferon-kappa Expression in Normal and HPV-positive Human Keratinocytes

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URI: http://hdl.handle.net/10900/101677
http://nbn-resolving.de/urn:nbn:de:bsz:21-dspace-1016771
http://dx.doi.org/10.15496/publikation-43056
Dokumentart: Dissertation
Date: 2022-03-15
Language: English
Faculty: 7 Mathematisch-Naturwissenschaftliche Fakultät
Department: Biologie
Advisor: Stevanovic, Stefan (Prof. Dr.)
Day of Oral Examination: 2020-05-28
DDC Classifikation: 500 - Natural sciences and mathematics
570 - Life sciences; biology
Keywords: Humanes Papillomavirus , Interferon
Other Keywords:
type I interferon
interferon-kappa
keratinocytes
antiviral
HPV
License: Publishing license excluding print on demand
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Inhaltszusammenfassung:

Dissertation ist gesperrt bis 15. März 2022 !

Abstract:

Type I interferons (IFNs) mediate antiviral activity, modulate immune responses and have anti-tumor activity. They impart their activities by binding to the IFN-alpha receptor on the cell surface and inducing the expression of IFN-stimulated genes (ISGs). The best-studied type I IFNs, IFN-alpha and -beta, are only expressed at very low levels in the absence of appropriate stimuli but can be strongly induced in most cell types upon activation of pattern-recognition receptors (PRRs). In contrast, IFN-kappa, another type I IFN, is expressed in a constitutive and cell type-specific manner in keratinocytes and is only weakly induced by activation of PRRs. IFN-kappa possesses activity against high risk human papillomaviruses (HR-HPV) which infect keratinocytes and IFN-kappa expression is reduced by HR-HPVs. HR-HPV represent a major health issue as they are one of the most frequently sexually transmitted infectious agents and cause virtually all cervical carcinomas, the world’s third most common cancer in women, which leads to more than 300,000 deaths per year. In the present work, regulatory mechanisms underlying the unusual pattern of IFN-kappa expression have been uncovered, using both normal and HPV16-positive human keratinocytes. It could be shown that IFN-kappa expression is mediated by the transcription factors AP-2alpha and p63, which are critically involved in keratinocyte biology and might explain the cell type-specific expression of this IFN. In addition, two signaling pathways which fine-tune IFN-kappa expression have been identified: TGF-beta1 signaling increases whereas ERK1/2 activity decreases IFN-kappa and ISG expression, both in normal and HPV16-positive keratinocytes, suggesting that IFN-kappa expression can be manipulated in pathological settings. Furthermore, increased IFN-kappa and ISG expression in HPV16-positive keratinocytes was accompanied by a decrease in viral transcription.

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