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The Antimicrobial Protein Psoriasin (S100A7) Is Upregulated in Atopic Dermatitis and after Experimental Skin Barrier Disruption  Regine Gläser, Ulf Meyer-Hoffert,

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Presentation on theme: "The Antimicrobial Protein Psoriasin (S100A7) Is Upregulated in Atopic Dermatitis and after Experimental Skin Barrier Disruption  Regine Gläser, Ulf Meyer-Hoffert,"— Presentation transcript:

1 The Antimicrobial Protein Psoriasin (S100A7) Is Upregulated in Atopic Dermatitis and after Experimental Skin Barrier Disruption  Regine Gläser, Ulf Meyer-Hoffert, Jürgen Harder, Jesko Cordes, Maike Wittersheim, Julia Kobliakova, Regina Fölster-Holst, Ehrhardt Proksch, Jens-Michael Schröder, Thomas Schwarz  Journal of Investigative Dermatology  Volume 129, Issue 3, Pages (March 2009) DOI: /jid Copyright © 2009 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 Psoriasin immunoreactivity is enhanced in lesional atopic dermatitis skin. (a) To localize the expression of psoriasin in human skin biopsies of AD patients and normal controls immunohistochemical staining was performed. Lesional skin of AD patients revealed increased psoriasin expression compared to nonlesional skin and healthy controls at correlating sites. Bars indicate 50μm. (b) Specificity testing was performed by preincubation of the antibody with various concentrations of natural skin-derived psoriasin. Blocking the antibody with higher concentrations than 0.06μg psoriasin resulted in complete inhibition of immunoreactivity in a tissue sample derived from the face of a healthy person. Immunostaining of psoriasis vulgaris served as a further positive control. Bars indicate 50μm. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2009 The Society for Investigative Dermatology, Inc Terms and Conditions

3 Figure 2 High concentrations of psoriasin are secreted in atopic dermatitis (AD) skin. A defined area (0.55cm2) of the skin of AD patients and matching normal controls was rinsed with sodium-phosphate buffer (pH 7.4). Soluble psoriasin concentrations were determined using a psoriasin-specific ELISA with two mAbs generated against natural psoriasin. Each sample was tested in triplicates. Bars indicate the median concentration. Groups were compared using the Wilcoxon matched pairs test (n=12). Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2009 The Society for Investigative Dermatology, Inc Terms and Conditions

4 Figure 3 TNF-α induced psoriasin secretion is inhibited by Th2 cytokines and Th17 cytokines induce psoriasin secretion in primary keratinocytes. (a, b) Psoriasin concentration was measured by ELISA in the supernatants of cultured primary keratinocytes after incubation with different cytokines (TNF-α, IL-4, and -13: 50ng/ml, IL-17, and -22: 20ng/ml) for 16hour. One representative out of three independent experiments is shown. Each stimulation was performed in triplicates. Bars indicate the SEM. Significance levels were determined in comparison to “TNF-α-values” (a) or the medium control (b) using the unpaired Student's t-test. *P<0.05; **P<0.01. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2009 The Society for Investigative Dermatology, Inc Terms and Conditions

5 Figure 4 Psoriasin secretion is enhanced after experimental disruption of the skin barrier in healthy persons. (a) A defined area (0.55cm2) of the forearm skin of healthy volunteers (n=12) was rinsed with sodium-phosphate buffer (pH 7.4) before (“control”) and after tape stripping at indicated time points. Psoriasin concentration in 1,000μl washing fluid was determined using a psoriasin-specific ELISA. Each sample was tested in triplicates. Bars indicate the median concentration. All time points were compared to the control values using the Wilcoxon matched pairs test. *P<0.05. (b) A defined area (0.55cm2) of both forearms of healthy volunteers (n=8) was rinsed with sodium-phosphate buffer (pH 7.4) before (“control”) and after tape stripping at indicated time points and the test area of one arm was held under occlusion for 24hour. Psoriasin concentration in the washing fluids was determined as indicated in (a). Both time points under investigation were compared to the control values using the Wilcoxon matched pairs test. *P<0.05, **P<0.01. (c) Immunohistochemical analysis of psoriasin expression in skin biopsies taken 24hour after experimental skin barrier disruption by tape stripping without and under occlusion in comparison to the untreated control at the same localization (forearm). The upper and lower panels represent two different individuals. Bars indicate 50μm. SC: Stratum corneum, E: epidermis, HF: hair follicle. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2009 The Society for Investigative Dermatology, Inc Terms and Conditions

6 Figure 5 Experimental setting of the in vivo experiments to determine the active secretion of antimicrobial psoriasin. (a) Determination of the transepidermal water loss (TEWL) of a standardized area on the forearm before and during skin barrier disruption. (b) Serial tape-stripping to reach a TEWL of 40g/m2 per hour. (c) Collection of washing fluids derived from the untreated forearm and the pretreated area at different time points. (d) Additional occlusion experiments were performed using Finn Chambers on Scanpor. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2009 The Society for Investigative Dermatology, Inc Terms and Conditions

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