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Helmholtz Zentrum für Infektionsforschung Repository > Division of Microbiology (MIK) > Dept. Vaccinology (VAC) > publications of the RG Immunalterung und chronische Infektion (IMCI) > Expression of S100A8/A9 in HaCaT keratinocytes alters the rate of cell proliferation and differentiation.


Please use this identifier to cite or link to this item: http://hdl.handle.net/10033/202630
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Title: Expression of S100A8/A9 in HaCaT keratinocytes alters the rate of cell proliferation and differentiation.
Authors: Voss, Andreas
Bode, Günther
Sopalla, Claudia
Benedyk, Malgorzata
Varga, Georg
Böhm, Markus
Nacken, Wolfgang
Kerkhoff, Claus
Affiliation: Institute of Immunology, University of Muenster, Muenster, Germany.
Citation: Expression of S100A8/A9 in HaCaT keratinocytes alters the rate of cell proliferation and differentiation. 2011, 585 (2):440-6 FEBS Lett.
Journal: FEBS letters
Issue Date: 21-Jan-2011
URI: http://hdl.handle.net/10033/202630
DOI: 10.1016/j.febslet.2010.12.037
PubMed ID: 21192933
Abstract: S100A8/A9 promotes NADPH oxidase in HaCaT keratinocytes and subsequently increases NFκB activation, which plays important roles in the balance between epidermal growth and differentiation. S100A8/A9-positive HaCaT cells present with a significantly reduced rate of cell division and greater expression of two keratinocyte differentiation markers, involucrin and filaggrin, than control cells. S100A8/A9 mutants fail to enhance NFκB activation, TNFα-induced IL-8 gene expression and NFκB p65 phosphorylation, and S100A8/A9-positive cells demonstrate better cell survival in forced suspension culture than mutant cells. S100A8/A9 is induced in epithelial cells in response to stress. Therefore, S100A8/A9-mediated growth arrest could have implications for tissue remodeling and repair.
Type: Article
Language: en
MeSH: Adaptation, Physiological
Calgranulin A
Calgranulin B
Cell Differentiation
Cell Line
Cell Proliferation
Epithelial Cells
Humans
Keratinocytes
NF-kappa B
ISSN: 1873-3468
Appears in Collections: publications of the RG Immunalterung und chronische Infektion (IMCI)

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