14-3-3ε protein increases matrix metalloproteinase-2 gene expression via p38 MAPK signaling in NIH3T3 fibroblast cells

被引:13
作者
Lee, Eun Kyung [1 ,2 ]
Lee, Youn Sook [1 ]
Lee, Hansol [3 ]
Choi, Cheol Yong [1 ]
Park, Seok Hee [1 ]
机构
[1] Sungkyunkwan Univ, Dept Biol Sci, Suwon 440746, South Korea
[2] Inha Univ, Coll Med, Inchon 400121, South Korea
[3] Inha Univ, Dept Biol Sci, Inchon 402751, South Korea
关键词
14-3-3; proteins; extracellular matrix; matrix metalloproteinase 2; p38 mitogen-activated protein kinases; signal transduction; skin aging; II RECEPTOR GENE; SKIN IN-VIVO; DERMAL FIBROBLASTS; COLLAGENASE; GROWTH; MODULATION; TGF-BETA-1; MIGRATION; LIGHT;
D O I
10.3858/emm.2009.41.7.050
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
One of the 14-3-3 protein isoforms, 14-3-3 epsilon, was previously shown to be increased during skin aging. We suggest here a possible role for the 14-3-3 epsilon protein in skin aging by providing evidence that 14-3-3 epsilon increases the expression of the matrix-metalloproteinase (MMP)-2 gene in NIH3T3 fibroblast cells. Expression of the 14-3-3 epsilon gene in NIH3T3 cells primarily up-regulated the expression of the MMP-2 gene at the transcriptional level by inducing specific DNA binding proteins bound to an upstream region of the MMP-2 promoter from -1,629 to -1,612. Inhibition of endogenous 14-3-3 epsilon gene expression by RNA interference also decreased endogenous MMP-2 gene expression. Furthermore, up-regulation of the MMP-2 gene by 14-3-3 epsilon was suppressed by expression of a dominant-negative mutant of p38 MAP kinase. These findings strongly suggest that increased expression of 14-3-3 epsilon contributes to remodeling of extracellular matrix in skin through increasing MMP-2 gene expression via p38 MAP kinase signaling.
引用
收藏
页码:453 / 461
页数:9
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