Please use this identifier to cite or link to this item:
http://dx.doi.org/10.25673/85874
Title: | Expression and activity of IL-17 receptor subunits in human cutaneous cells as targets for anti-IL-17 therapeutic antibodies |
Author(s): | Wohlrab, Johannes Gerloff, Dennis Gebhardt, Kathleen |
Issue Date: | 2022 |
Type: | Article |
Language: | English |
Abstract: | The key players in different chronic inflammatory skin diseases are cytokines belonging to the IL-17 group, IL-17 receptors and a T helper cell population, Th17 cells. Successful therapeutic strategies that target either IL-17 or the major IL-17 receptor IL-17RA have confirmed the immune-pathogenic pathway. To study the IL-17-ligand – receptor axis at the molecular level, a number of cutaneous cell types from healthy human subjects has been cultured and analyzed for the expression of IL-17 receptors. IL-17RA was the most abundantly expressed receptor type in keratinocytes, epidermal stem cells, fibroblasts, mesenchymal stem cells, hemo- and lymphovascular endothelial cells. IL-17RC and IL-17RD showed moderate expression, while the genes for IL-17RB and IL-17RE were poorly expressed. In none of the investigated cell types, IL-17 ligands caused an increased expression level of the five receptor types in time- and dose-dependent experiments. No evidence for IL-17A, -C, -E or -F induced signal transduction cascades could be obtained by a qRT-PCR and western blot analyses. Further studies are necessary to identify relevant co-stimulating factors from IL-17 subtypes under physiological and pathophysiological conditions. |
URI: | https://opendata.uni-halle.de//handle/1981185920/87826 http://dx.doi.org/10.25673/85874 |
Open Access: | Open access publication |
License: | (CC BY 4.0) Creative Commons Attribution 4.0 |
Sponsor/Funder: | Publikationsfonds MLU |
Journal Title: | Biomedicine & pharmacotherapy |
Publisher: | Elsevier Science |
Publisher Place: | Amsterdam [u.a.] |
Volume: | 146 |
Original Publication: | 10.1016/j.biopha.2021.112569 |
Appears in Collections: | Open Access Publikationen der MLU |
Files in This Item:
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1-s2.0-S0753332221013561-main.pdf | 4.23 MB | Adobe PDF | View/Open |