Lack of plakoglobin in epidermis leads to keratoderma.

Abstract

Loss-of-function mutation of Jup has been associated with Naxos disease, which is characterized by arrhythmogenic cardiomyopathy and the cutaneous disorder palmoplantar keratoderma. Previously, we have shown that genetic ablation of Jup in cardiomyocytes in mice leads to arrhythmogenic cardiomyopathy similar to Naxos disease in humans. Currently, to determine the pathogenesis of Naxos disease-associated keratoderma, we generated Jup mutant mice by inactivating Jup restrictively in keratinocytes. Jup mutant mice largely recapitulated the clinical features of human palmoplantar keratoderma: overcornification and thickening of the epidermis. Jup mutant mice also suffered skin ulceration and inflammation. Cell apoptosis and proliferation were significantly elevated in Jup mutant epidermis. Ultrastructural analyses revealed the disruption of the assembly of desmosomes and adherens junctions in Jup mutant epidermis. We also demonstrated the compensational increase in β-catenin at Jup mutant cell-cell junctions without altering its signaling activities. Our findings provide important insights for understanding the pathogenesis of human palmoplantar keratoderma.

• Authors: Deqiang Li, Wenjun Zhang, Ying Liu, Laura S Haneline, Weinian Shou
• Journal: The Journal of biological chemistry (J Biol Chem) Vol. 287 Issue 13 Pg. 10435-10443 (Mar 23 2012) ISSN: 1083-351X [Electronic] United States
• PMID: 22315228 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Desmoplakins
• JUP protein, human
• Jup protein, mouse
• gamma Catenin

Topics

• Adherens Junctions (genetics, metabolism, ultrastructure)
• Animals
• Apoptosis
• Arrhythmogenic Right Ventricular Dysplasia (genetics, metabolism, pathology)
• Cell Proliferation
• Desmoplakins (genetics, metabolism)
• Desmosomes (genetics, metabolism, ultrastructure)
• Epidermis (metabolism, ultrastructure)
• Hair Diseases (genetics, metabolism, pathology)
• Humans
• Keratoderma, Palmoplantar (genetics, metabolism, pathology)
• Mice
• Mice, Transgenic
• gamma Catenin (genetics, metabolism)