Fibulin-4 regulates expression of the tropoelastin gene and consequent elastic-fibre formation by human fibroblasts

被引:14
作者
Chen, Qiuyun [1 ]
Zhang, Teng [1 ]
Roshetsky, Joseph F. [1 ]
Ouyang, Zhufeng [1 ]
Essers, Jeroen [2 ,3 ,4 ]
Fan, Chun [1 ]
Wang, Qing [1 ]
Hinek, Aleksander [5 ,6 ]
Plow, Edward F. [1 ]
DiCorleto, Paul E. [7 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Mol Cardiol, Cleveland, OH 44195 USA
[2] Erasmus MC, Dept Cell Biol & Genet, NL-3015GE Rotterdam, Netherlands
[3] Erasmus MC, Dept Radiat Oncol, NL-3015GE Rotterdam, Netherlands
[4] Erasmus MC, Dept Vasc Surg, NL-3015GE Rotterdam, Netherlands
[5] Univ Toronto, Hosp Sick Children, Ctr Heart, Toronto, ON M5G 1X8, Canada
[6] Univ Toronto, Dept Lab Med & Pathol, Toronto, ON M5G 1X8, Canada
[7] Cleveland Clin, Lerner Res Inst, Dept Cell Biol, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
elastic-fibre formation; elastin; extracellular-matrix protein; fibulin-4; human foreskin fibroblast; tropoelastin gene; WILLIAMS-BEUREN-SYNDROME; GROWTH-FACTOR-BETA; SUPRAVALVULAR AORTIC-STENOSIS; MESSENGER-RNA LEVELS; EXTRACELLULAR-MATRIX; COSTELLO-SYNDROME; BINDING-PROTEIN; DEVELOPMENTAL REGULATION; IMPAIRED ELASTOGENESIS; PERINATAL LETHALITY;
D O I
10.1042/BJ20090993
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
Elastic fibres are essential for normal physiology in numerous tissues, including arteries, lungs and skin. Fibulin-4 is an elastic-fibre-associated glycoprotein that is indispensable for elastic-fibre formation in mice. However, the mechanism by which fibulin-4 executes this function remains to be determined. Here, we established an in vitro functional assay system in which fibulin-4 was knocked down in human foreskin fibroblasts using siRNA (small interfering RNA) technology. With two different siRNAs, substantial knockdown of fibulin-4 was achieved, and this suppression was associated with impaired elastic-fibre formation by the fibroblasts. Real-time reverse transcription-PCR analysis showed that knockdown of fibulin-4 expression was accompanied by reduced expression of tropoelastin mRNA. Further analysis showed that this decrease was caused by transcriptional down-regulation of tropoelastin. This effect was selective, since the mRNA level of other elastic-fibre-associated proteins, including fibrillin-1, lysyl oxidase and lysyl oxidase-like-1, was not affected. Moreover, addition of conditioned medium from cultures of CHO (Chinese-hamster ovary) cells overexpressing fibulin-4 stimulated tropoelastin expression and elastic-fibre formation in cultures of Williams-Beuren-syndrome fibroblasts. Knocking down or knocking out fibulin-4 in mice led to a decrease in tropoelastin expression in the aorta. These results indicate that fibulin-4, considered as a structural protein, may also participate in regulating elastic-fibre formation in human cells through an unanticipated mechanism, namely the regulation of tropoelastin expression.
引用
收藏
页码:79 / 89
页数:11
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