The Differentiation-Associated Keratinocyte Protein Cornifelin Contributes to Cell-Cell Adhesion of Epidermal and Mucosal Keratinocytes.
Acantholysis
/ genetics
Cell Adhesion
Cell Differentiation
Cells, Cultured
Desmogleins
/ metabolism
Desmosomes
/ physiology
Epidermis
/ metabolism
Humans
Intercellular Signaling Peptides and Proteins
/ metabolism
Keratinocytes
/ physiology
Membrane Proteins
/ genetics
Mouth Mucosa
/ metabolism
Organ Culture Techniques
RNA, Small Interfering
/ genetics
Journal
The Journal of investigative dermatology
ISSN: 1523-1747
Titre abrégé: J Invest Dermatol
Pays: United States
ID NLM: 0426720
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
05
09
2018
revised:
05
04
2019
accepted:
14
04
2019
pubmed:
28
5
2019
medline:
9
6
2020
entrez:
27
5
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 31129056
pii: S0022-202X(19)31569-6
doi: 10.1016/j.jid.2019.04.019
pii:
doi:
Substances chimiques
CDSN protein, human
0
CNFN protein, human
0
Desmogleins
0
Intercellular Signaling Peptides and Proteins
0
Membrane Proteins
0
RNA, Small Interfering
0
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2292-2301.e9Informations de copyright
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.