HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

Abstract
Naegeli-Franceschetti-Jadassohn syndrome (NFJS) is a rare autosomal dominant disorder characterized by loss of dermatoglyphics, reticulate hyperpigmentation of the skin, palmoplantar keratoderma, abnormal sweating, and other developmental anomalies of the teeth, hair, and skin. We recently demonstrated that NFJS is caused by heterozygous nonsense or frameshift mutations in the E1/V1-encoding region of KRT14, but the mechanisms for their deleterious effects in NFJS remain elusive. In this study, we further expand the spectrum of NFJS-causing mutations and demonstrate that these mutations result in haploinsufficiency for keratin 14 (K14). As increased apoptotic activity was observed in the epidermal basal cell layer in NFJS patients and as previous data suggested that type I keratins may confer resistance to tumor necrosis factor-alpha (TNF-alpha)-induced apoptosis in epithelial tissues, we assessed the effect of down-regulation of KRT14 expression on apoptotic activity in keratinocytes. Using a HaCaT cell-based assay, we found that decreased KRT14 expression is associated with increased susceptibility to TNF-alpha-induced apoptosis. This phenomenon was not observed when cells were cultured in the presence of doxycycline, a known negative regulator of TNF-alpha-dependant pro-apoptotic signaling. Collectively, our results indicate that NFJS results from haploinsufficiency for K14 and suggest that increased susceptibility of keratinocytes to pro-apoptotic signals may be involved in the pathogenesis of this ectodermal dysplasia syndrome.
AuthorsJennie Lugassy, John A McGrath, Peter Itin, Revital Shemer, Julian Verbov, Helen R Murphy, Akemi Ishida-Yamamoto, John J Digiovanna, Dani Bercovich, Nathan Karin, Alon Vitenshtein, Jouni Uitto, Reuven Bergman, Gabriele Richard, Eli Sprecher
JournalThe Journal of investigative dermatology (J Invest Dermatol) Vol. 128 Issue 6 Pg. 1517-24 (Jun 2008) ISSN: 1523-1747 [Electronic] United States
PMID18049449 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Keratin-14
  • Tumor Necrosis Factor-alpha
  • Keratins
Topics
  • Apoptosis
  • Cell Line
  • Child
  • Female
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Humans
  • Keratin-14 (genetics, physiology)
  • Keratinocytes (metabolism)
  • Keratins (metabolism)
  • Mutation
  • Skin Abnormalities (metabolism)
  • Skin Diseases (genetics)
  • Syndrome
  • Tumor Necrosis Factor-alpha (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: