The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions

• Published in: International journal of molecular sciences Vol. 23; no. 13; p. 7486
• Main Authors: Haftek, Marek, Oji, Vinzenz, Feldmeyer, Laurence, Hohl, Daniel, Hadj-Rabia, Smaïl, Abdayem, Rawad
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-07-2022; MDPI
• Subjects: Abdomen; Acids; Acne; Antibodies; Biopsy; Cholangitis; desquamation; Electron microscopy; Epidermis; Explants; Ichthyosis; ichthyosis hypotrichosis sclerosing cholangitis (IHSC/NISCH) syndrome; Lipids; Membranes; Microscopy; peeling skin disease (PSD); Permeability; Proteins; Salicylic acid; Skin diseases; Stratum corneum; tight junction; Tight junctions; ultrastructure
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23137486

We evaluated the presence of tight junction (TJ) remnants in the stratum corneum (SC) of in vitro reconstructed human epidermis and human skin explants subjected or not to an aggressive topical treatment with beta-lipohydroxy salicylic acid (LSA) for 24 h. LSA-treated samples showed an increased presence of TJ remnants in the two lowermost layers of the SC, as quantified with standard electron microscopy. The topical aggression-induced overexpression of TJ-like cell–cell envelope fusions may influence SC functions: (1) directly, through an enhanced cohesion, and (2) indirectly, by impeding accessibility of peripheral corneodesmosomes to extracellular hydrolytic enzymes and, thus, slowing down desquamation. Observations of ichthyotic epidermis in peeling skin disease (PSD; corneodesmosin deficiency; two cases) and ichthyosis hypotrichosis sclerosing cholangitis syndrome (IHSC/NISCH; absence of claudin-1; two cases) also demonstrated increased persistence of TJ-like intercellular fusions in pathological SC and contributed to the interpretation of the diseases’ pathological mechanisms.