Institute of Immunology, University of Muenster, Muenster, Germany.
FEBS Lett. 2011 Jan 21;585(2):440-6. doi: 10.1016/j.febslet.2010.12.037. Epub 2010 Dec 28.
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.
S100A8/A9 可促进 HaCaT 角质细胞中的 NADPH 氧化酶,从而增加 NFκB 的激活,这在表皮生长和分化的平衡中起着重要作用。S100A8/A9 阳性 HaCaT 细胞的细胞分裂速度明显降低,两种角蛋白分化标志物——包裹蛋白和丝聚合蛋白的表达水平显著升高,高于对照细胞。S100A8/A9 突变体不能增强 NFκB 的激活、TNFα 诱导的 IL-8 基因表达和 NFκB p65 磷酸化,S100A8/A9 阳性细胞在强制悬浮培养中的细胞存活率优于突变细胞。S100A8/A9 是上皮细胞在应激反应中诱导产生的。因此,S100A8/A9 介导的生长停滞可能与组织重塑和修复有关。