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Rockefeller University Press, Journal of Cell Biology, 7(179), p. 1599-1612, 2007

DOI: 10.1083/jcb.200706187

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Mice deficient in involucrin, envoplakin, and periplakin have a defective epidermal barrier

Journal article published in 2007 by Lisa M. Sevilla, Rachida Nachat, Karen R. Groot, John F. Klement, Jouni Uitto, Philippe Djian, Arto Määttä, Fiona M. Watt ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The cornified envelope is assembled from transglutaminase cross-linked proteins and lipids in the outermost epidermal layers and is essential for skin barrier function. Involucrin, envoplakin, and periplakin form the protein scaffold on which the envelope assembles. To examine their combined function, we generated mice deficient in all three genes. The triple knockouts have delayed embryonic barrier formation and postnatal hyperkeratosis (abnormal accumulation of cornified cells) resulting from impaired desquamation. Cornified envelopes form but are ultrastructurally abnormal, with reduced lipid content and decreased mechanical integrity. Expression of proteases is reduced and the protease inhibitor, serpina1b, is highly upregulated, resulting in defective filaggrin processing and delayed degradation of desmoglein 1 and corneodesmosin. There is infiltration of CD4+ T cells and a reduction in resident gammadelta+ T cells, reminiscent of atopic dermatitis. Thus, combined loss of the cornified envelope proteins not only impairs the epidermal barrier, but also changes the composition of T cell subpopulations in the skin.