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Expression of S100A8/A9 in HaCaT keratinocytes alters the rate of cell proliferation and differentiation
被引:40
|作者:
Voss, Andreas
[1
]
Bode, Guenther
[1
]
Sopalla, Claudia
[1
]
Benedyk, Malgorzata
[1
]
Varga, Georg
[1
,2
]
Boehm, Markus
[2
]
Nacken, Wolfgang
[3
]
Kerkhoff, Claus
[1
]
机构:
[1] Univ Munster, Inst Immunol, D-4400 Munster, Germany
[2] Univ Munster, Dept Dermatol, D-4400 Munster, Germany
[3] Univ Munster, Inst Mol Virol, ZMBE, D-4400 Munster, Germany
来源:
FEBS LETTERS
|
2011年
/
585卷
/
02期
关键词:
S100;
protein;
Epithelial cell;
Stress response;
Cell growth;
Cell differentiation;
NF kappa B activation;
NF-KAPPA-B;
BINDING-PROTEINS;
ARACHIDONIC-ACID;
NADPH OXIDASE;
SKIN;
ACTIVATION;
KINASE;
CANCER;
GENES;
MICE;
D O I:
10.1016/j.febslet.2010.12.037
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
S100A8/A9 promotes NADPH oxidase in HaCaT keratinocytes and subsequently increases NF kappa B 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 NF kappa B activation, TNF alpha-induced IL-8 gene expression and NF kappa B 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. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:440 / 446
页数:7
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