1. The Differentiation-Associated Keratinocyte Protein Cornifelin Contributes to Cell-Cell Adhesion of Epidermal and Mucosal Keratinocytes
- Author
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Maria Gschwandtner, Adolf Ellinger, Michael Mildner, Tanja Wagner, Polina Kalinina, Maria Laggner, Erwin Tschachler, Leopold Eckhart, Bahar Golabi, Reinhard Gruber, Lucian Beer, and Ulrike Kuchler
- Subjects
Keratinocytes ,0301 basic medicine ,Human skin ,Dermatology ,Biochemistry ,03 medical and health sciences ,Organ Culture Techniques ,0302 clinical medicine ,Cell Adhesion ,Stratum corneum ,medicine ,Humans ,RNA, Small Interfering ,Oral mucosa ,Cell adhesion ,Molecular Biology ,Cells, Cultured ,Corneocyte ,integumentary system ,Epidermis (botany) ,Chemistry ,Acantholysis ,Mouth Mucosa ,Membrane Proteins ,Cell Differentiation ,Desmosomes ,Cell Biology ,medicine.disease ,Cell biology ,030104 developmental biology ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Intercellular Signaling Peptides and Proteins ,Epidermis ,Desmogleins ,Keratinocyte - Abstract
Cornifelin (CNFN) has been identified as a protein component of epidermal corneocytes. Here, we investigated the tissue distribution of CNFN and potential consequences of CNFN deficiency on epithelial function in in vitro models of human skin and oral mucosa. Our detailed bioinformatics and immunostaining analysis revealed that CNFN is not only expressed in human epidermis but also in noncornifying oral mucosa. In normal epidermis, CNFN was confined to the upper granular layer and the stratum corneum. By contrast, in both partly cornifying and noncornifying oral mucosa, CNFN was expressed in a cell membrane-associated pattern over several suprabasal layers. Small interfering RNA-mediated knockdown of CNFN in epidermal keratinocytes (KCs) was associated with only subtle alterations of the overall epidermal architecture in skin models in vitro but led to altered morphology of corneodesmosomes, as detected by electron microscopy. Using dispase treatment followed by mechanical stress, epithelial sheets of CNFN-deficient epidermal KCs were easily disrupted, whereas their CNFN-competent counterparts remained intact. In contrast to the epidermal KCs, CNFN knockdown in oral KCs had a more severe effect and caused pronounced acantholysis in organotypic models of oral mucosa. Together, these findings indicate that CNFN is a structural component of the cell adhesion system of differentiated KCs in both epidermis and oral mucosa.
- Published
- 2019
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