Establishment of Two Mouse Models for CEDNIK Syndrome Reveals the Pivotal Role of SNAP29 in Epidermal Differentiation

2016 | journal article. A publication with affiliation to the University of Göttingen.

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​Establishment of Two Mouse Models for CEDNIK Syndrome Reveals the Pivotal Role of SNAP29 in Epidermal Differentiation​
Schiller, S. A.; Seebode, C.; Wieser, G. L.; Goebbels, S.; Möbius, W. ; Horowitz, M. & Sarig, O. et al.​ (2016) 
Journal of Investigative Dermatology136(3) pp. 672​-679​.​ DOI: 

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Schiller, Stina A.; Seebode, Christina; Wieser, Georg L.; Goebbels, Sandra; Möbius, Wiebke ; Horowitz, Mia; Sarig, Ofer; Sprecher, Eli; Emmert, Steffen
Loss-of-function mutations in the synaptosomal-associated protein 29 (SNAP29) gene cause the cerebral dysgenesis, neuropathy, ichthyosis, and keratoderma syndrome. In this study, we created total (Snap29(-/-)) as well as keratinocyte-specific (Snap29(fl/fl)/K14-Cre) Snap29 knockout mice. Both mutant mice exhibited a congenital distinct ichthyotic phenotype resulting in neonatal lethality. Mutant mice revealed acanthosis and hyperkeratosis as well as abnormal keratinocyte differentiation and increased proliferation. In addition, the epidermal barrier was severely impaired. These results indicate an essential role of SNAP29 in epidermal differentiation and barrier formation. Markedly decreased deposition of lamellar body contents in mutant mice epidermis and the observation of malformed lamellar bodies indicate severe impairments in lamellar body function due to the Snap29 knockout. We also found increased microtubule associated protein-1 light chain 3, isoform B-II levels, unchanged p62/SQSTM1 protein amounts, and strong induction of the endoplasmic reticulum stress marker C/EBP homologous protein in mutant mice. This emphasizes a role of SNAP29 in autophagy and endoplasmic reticulum stress. Our murine models serve as powerful tools for investigating keratinocyte differentiation processes and provide insights into the essential contribution of SNAP29 to epidermal differentiation.
Issue Date
Nature Publishing Group
Journal of Investigative Dermatology 
1523-1747; 0022-202X



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