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The Role of Galectin-9 as Mediator of Atopic Dermatitis: Effect on Keratinocytes.
- Source :
-
Cells [Cells] 2021 Apr 20; Vol. 10 (4). Date of Electronic Publication: 2021 Apr 20. - Publication Year :
- 2021
-
Abstract
- Galectin-9 (Gal-9) is a beta-galactoside-binding protein with a variety of biological functions related to immune response. However, in allergic diseases, its mechanism of action is not fully understood. This study evaluates the expression pattern of Gal-9 in patients with atopic dermatitis (AD), in ovalbumin (OVA)-induced experimental atopic dermatitis (AD) in mice, as well as its effect on human keratinocytes. The skin of OVA-immunized BALB/c mice was challenged with drops containing OVA on days 11, 14-18, and 21-24. HaCaT cells were cultured in the following experimental conditions: control (growth medium only) or stimulated with TNF-α/IFN-γ, or IL-4, or IL-17 with or without Gal-9 treatment. AD was characterized by increased levels of Gal-9 in mouse and human skin, especially in the epidermis, and with a marked influx of Gal-9 positive eosinophils and mast cells compared to the control group. Gal-9 showed an immunomodulatory effect on keratinocytes by decreasing the release of IL-6 by IL-4-stimulated keratinocytes or increasing the IL-6 and RANTES levels by IL-17- or TNF-α/IFN-γ-stimulated cells, respectively. Under IL-17, Gal-9 treatment also altered the proliferation rate of cells. Overall, increased levels of Gal-9 in AD skin contribute to the control of inflammatory response and the proliferative process of keratinocytes, suggesting this lectin as a relevant therapeutic target.
- Subjects :
- Animals
Cell Movement
Cell Proliferation
Cytokines metabolism
Disease Models, Animal
Humans
Inflammation pathology
Male
Mice, Inbred BALB C
Skin pathology
Up-Regulation genetics
Mice
Dermatitis, Atopic metabolism
Dermatitis, Atopic pathology
Galectins metabolism
Keratinocytes metabolism
Keratinocytes pathology
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 10
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 33923930
- Full Text :
- https://doi.org/10.3390/cells10040947