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    • Original Article
      Open Access

      Identification of Keratinocyte Mitogens: Implications for Hyperproliferation in Psoriasis and Atopic Dermatitis

      JID Innovations
      Vol. 2Issue 1100066Published online: October 21, 2021
      • Hanna Niehues
      • Gijs Rikken
      • Ivonne M.J.J. van Vlijmen-Willems
      • Diana Rodijk-Olthuis
      • Piet E.J. van Erp
      • Patrick L.J.M. Zeeuwen
      • and others
      Cited in Scopus: 0
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        Psoriasis and atopic dermatitis are chronic inflammatory skin diseases characterized by keratinocyte (KC) hyperproliferation and epidermal acanthosis (hyperplasia). The milieu of disease-associated cytokines and soluble factors is considered a mitogenic factor; however, pinpointing the exact mitogens in this complex microenvironment is challenging. We employed organotypic human epidermal equivalents, faithfully mimicking native epidermal proliferation and stratification, to evaluate the proliferative effects of a broad panel of (literature-based) potential mitogens.
        Identification of Keratinocyte Mitogens: Implications for Hyperproliferation in Psoriasis and Atopic Dermatitis
      • Original Article
        Open Access

        Deletion of TNFAIP6 Gene in Human Keratinocytes Demonstrates a Role for TSG-6 to Retain Hyaluronan Inside Epidermis

        JID Innovations
        Vol. 1Issue 4100054Published online: August 23, 2021
        • Céline Evrard
        • Emilie Faway
        • Evelyne De Vuyst
        • Olivier Svensek
        • Valérie De Glas
        • David Bergerat
        • and others
        Cited in Scopus: 0
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          TSG-6 is a soluble protein secreted in the extracellular matrix by various cell types in response to inflammatory stimuli. TSG-6 interacts with extracellular matrix molecules, particularly hyaluronan (HA), and promotes cutaneous wound closure in mice. Between epidermal cells, the discrete extracellular matrix contains HA and a tiny amount of TSG-6. However, challenges imposed to keratinocytes in reconstructed human epidermis revealed strong induction of TSG-6 expression, after exposure to T helper type 2 cytokines to recapitulate the atopic dermatitis phenotype or after fungal infection that causes secretion of cytokines and antimicrobial peptides.
          Deletion of TNFAIP6 Gene in Human Keratinocytes Demonstrates a Role for TSG-6 to Retain Hyaluronan Inside Epidermis
        • Review
          Open Access

          Cracking the Skin Barrier: Liquid-Liquid Phase Separation Shines under the Skin

          JID Innovations
          Vol. 1Issue 3100036Published online: July 5, 2021
          • Alexa Regina Chua Avecilla
          • Felipe Garcia Quiroz
          Cited in Scopus: 0
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            Central to forming and sustaining the skin’s barrier, epidermal keratinocytes (KCs) fluxing to the skin surface undergo a rapid and enigmatic transformation into flat, enucleated squames. At the crux of this transformation are intracellular keratohyalin granules (KGs) that suddenly disappear as terminally differentiating KCs transition to the cornified skin surface. Defects in KGs have long been linked to skin barrier disorders. Through the biophysical lens of liquid-liquid phase separation (LLPS), these enigmatic KGs recently emerged as liquid-like membraneless organelles whose assembly and subsequent pH-triggered disassembly drive squame formation.
            Cracking the Skin Barrier: Liquid-Liquid Phase Separation Shines under the Skin
          • Original Article
            Open Access

            Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis

            JID Innovations
            Vol. 1Issue 3100033Published online: June 14, 2021
            • Petra Pavel
            • Géraldine Leman
            • Martin Hermann
            • Christian Ploner
            • Thomas O. Eichmann
            • Deborah Minzaghi
            • and others
            Cited in Scopus: 0
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              Alterations of the lipid profile of the stratum corneum have an important role in the pathogenesis of atopic dermatitis (AD) because they contribute to epidermal barrier impairment. However, they have not previously been envisioned as a cellular response to altered metabolic requirements in AD epidermis. In this study, we report that the lipid composition in the epidermis of flaky tail, that is, ft/ft mice mimics that of human lesional AD (ADL) epidermis, both showing a shift toward shorter lipid species.
              Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis
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