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Publication : Impaired NF-kappa B activation and increased production of tumor necrosis factor alpha in transgenic mice expressing keratin K10 in the basal layer of the epidermis.

First Author  Santos M Year  2003
Journal  J Biol Chem Volume  278
Issue  15 Pages  13422-30
PubMed ID  12566451 Mgi Jnum  J:82950
Mgi Id  MGI:2656111 Doi  10.1074/jbc.M208170200
Citation  Santos M, et al. (2003) Impaired NF-kappa B Activation and Increased Production of Tumor Necrosis Factor alpha in Transgenic Mice Expressing Keratin K10 in the Basal Layer of the Epidermis. J Biol Chem 278(15):13422-30
abstractText  Both the diversity and the precisely regulated tissue- and differentiation-specific expression patterns of keratins suggest that these proteins have specific functions in epithelia besides their well known maintenance of cell integrity. In the search for these specific functions, our previous results have demonstrated that the expression of K10, a keratin expressed in postmitotic suprabasal cells of the epidermis, prevents cell proliferation through the inhibition of Akt kinase activity. Given the roles of Akt in NF-kappaB signaling and the importance of these processes in the epidermis, a study was made into the possible alterations of the NF-kappaB pathway in transgenic mice expressing K10 in the proliferative basal layer. It was found that the inhibition of Akt, mediated by K10 expression, leads to impaired NF-kappaB activity. This appears to occur through the decreased expression of IKKbeta and IKKgamma. Remarkably, increased production of tumor necrosis factor alpha and concomitant JNK activation was observed in the epidermis of these transgenic mice. These results confirm that keratin K10 functions in vivo include the control of many aspects of epithelial physiology, which affect the cells not only in a cell autonomous manner but also influence tissue homeostasis.
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